Polycystin 2 is increased in disease to protect against stress-induced cell death

Brill, Allison L.; Fischer, Tom T.; Walters, Jennifer M.; Marlier, Arnaud; Sewanan, Lorenzo R.; Wilson, Parker C.; Johnson, Eric K.; Moeckel, Gilbert; Cantley, Lloyd G.; Campbell, Stuart G.; Nerbonne, Jeanne M.; Chung, Hee Jung; Robert, Marie E.; Ehrlich, Barbara E.

doi:10.1038/s41598-019-57286-x

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Published: 15 January 2020

Polycystin 2 is increased in disease to protect against stress-induced cell death

Allison L. Brill ORCID: orcid.org/0000-0002-5046-3578¹,
Tom T. Fischer ORCID: orcid.org/0000-0002-2138-9102^2,3,
Jennifer M. Walters^4,5,
Arnaud Marlier⁶,
Lorenzo R. Sewanan⁷,
Parker C. Wilson⁸^nAff11,
Eric K. Johnson⁹,
Gilbert Moeckel⁸,
Lloyd G. Cantley⁶,
Stuart G. Campbell⁷,
Jeanne M. Nerbonne ORCID: orcid.org/0000-0001-8334-8499^9,10,
Hee Jung Chung^4,5,
Marie E. Robert⁸ &
…
Barbara E. Ehrlich ORCID: orcid.org/0000-0001-9657-9704^1,2

Scientific Reports volume 10, Article number: 386 (2020) Cite this article

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Abstract

Polycystin 2 (PC2 or TRPP1, formerly TRPP2) is a calcium-permeant Transient Receptor Potential (TRP) cation channel expressed primarily on the endoplasmic reticulum (ER) membrane and primary cilia of all cell and tissue types. Despite its ubiquitous expression throughout the body, studies of PC2 have focused primarily on its role in the kidney, as mutations in PC2 lead to the development of autosomal dominant polycystic kidney disease (ADPKD), a debilitating condition for which there is no cure. However, the endogenous role that PC2 plays in the regulation of general cellular homeostasis remains unclear. In this study, we measure how PC2 expression changes in different pathological states, determine that its abundance is increased under conditions of cellular stress in multiple tissues including human disease, and conclude that PC2-deficient cells have increased susceptibility to cell death induced by stress. Our results offer new insight into the normal function of PC2 as a ubiquitous stress-sensitive protein whose expression is up-regulated in response to cell stress to protect against pathological cell death in multiple diseases.

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Introduction

Polycystin-2 (PC2 or TRPP1, formerly TRPP2) is a Transient Receptor Potential (TRP) channel most well-known for its associated pathology. When mutated, PC2 causes autosomal dominant polycystic kidney disease (ADPKD), a debilitating condition leading to bilateral renal cyst formation and eventual kidney failure¹. Located primarily on the endoplasmic reticulum (ER) and primary cilia of all cell and tissue types^2,3,4,5, PC2 is a calcium (Ca²⁺)-permeant cation channel whose expression level directly affects Ca²⁺ release from the ER⁵. As such, PC2 is thought to play a key role in regulating Ca²⁺-regulated homeostasis and signaling pathways⁶. This is supported by findings showing that polycystin-deficient cells exhibit dysregulated Ca²⁺ mobilization and Ca²⁺-regulated signaling pathways^5,7, including pathologically increased cAMP levels^8,9 and changes in mitochondrial Ca²⁺ uptake^10,11. The aberrant Ca²⁺ signaling caused by loss of polycystins is therefore often pointed to as a central cause of enhanced apoptosis^12,13, excess fluid secretion^14,15, and metabolic abnormalities^{10,11,16,17,18} seen in cystic kidney cells. Given the importance of PC2 in ADPKD development, most studies of PC2 have focused on its function in the kidney. However, the ubiquitous expression of PC2 in all cell types suggests that it is important in maintaining Ca²⁺ homeostasis in tissues beyond the kidney.

The tight regulation of intracellular Ca²⁺ is necessary for many physiological functions, including protecting cells against outside stressors. Oxidative and ER stress responses require Ca²⁺ influx from both the extracellular environment and intracellular stores as a key initial step for combating cell damage^19,20,21,22. This elevated intracellular Ca²⁺ coordinates many physiological functions, such as changes in Ca²⁺-dependent gene transcription and activation of pro-survival pathways²³. Because altered Ca²⁺ signaling occurs in cells with differential PC2 expression⁵, it follows that cells with changed PC2 levels may exhibit altered cellular homeostasis in response to stress. Indeed, beyond ADPKD, the polycystins have been linked to multiple extrarenal pathologies involving dysregulated Ca²⁺ and stress, including the development of liver²⁴ and pancreatic²⁵ cysts, cerebral aneurysms^26,27, cardiac disease²⁸, and cancer²⁹. For instance, increased PC2 levels enhance colorectal cancer aggressiveness via modulation of cancer cell proliferation and migration through aberrant Ca²⁺-modulated signaling pathways³⁰. Conversely, decreased PC2 corresponds to increased interstitial fibrosis and heightened sensitivity to injury in response to kidney ischemia³¹. It is established that the gene encoding for PC2, Pkd2, is differentially expressed during animal development to coordinate left-right axis determination in mice^32,33 and zebrafish³⁴. However, despite reports of altered PC2 expression in pathological states^31,35,36,37, the conditions under which PC2 levels are regulated after development and into adulthood remain incompletely understood. Furthermore, how transcriptionally-regulated changes in PC2 levels influence the cellular response to stress remains unexplored. An understanding of how PC2 levels are regulated in somatic cells will give further insight into its involvement in maintaining normal cellular homeostasis, and may provide potential new targets for the treatment of ADPKD and other diseases affected by polycystin or Ca²⁺ dysfunction.

Given that increased PC2 levels correlate with enhanced cell viability and proliferation³⁰, and that elevated Ca²⁺ promotes the activation of pro-survival pathways³⁸, we hypothesized that PC2 expression is enhanced under conditions of stress to help protect against cell death. In this study, we found that levels of PC2 increase in disease states with ER and oxidative stress. PC2 up-regulation occurred under pathological conditions in multiple tissue types, including the kidney, liver, brain, and hearts of both humans and animal models. Finally, PC2 knock-down and knock-out cells showed increased susceptibility to stress-induced cell death. Collectively, our results indicate that PC2 acts in all tissues as a ubiquitous stress response protein whose expression levels correlate with cell survival in response to stress.

Results

PC2 levels are increased in kidneys with acute kidney injury

As one of its main functions, PC2 modulates intracellular Ca²⁺ signaling. Studies demonstrate that the expression level of PC2 directly impacts the amount of ER Ca²⁺ released in response to inositol 1,4,5-trisphosphate (InsP3)-dependent stimuli^39,40,41. Because kidney tubules afflicted with ischemia-induced acute kidney injury (AKI) exhibit intracellular Ca²⁺ overload and altered Ca²⁺ dynamics⁴², we tested whether the expression level of PC2 was changed in AKI-afflicted kidneys. To model injury, mice were subjected to renal unilateral ischemia/reperfusion (I/R) injury with nephrectomy in which the right renal pedicle was clamped for 27 minutes, reperfused, then sacrificed 72 hours later and the right kidney collected. Left nephrectomized kidney was used as sham control (pre-injury). Increased 4-hydroxynonenal (4-HNE) and nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB), and degradation of inhibitor of kappa (IκBα) confirmed the induction of AKI in I/R kidneys compared to nephrectomy controls (Figs. 1A,B, S1A–C). Strikingly, PC2 abundance was also significantly increased in kidneys with I/R injury (Fig. 1A,C), consistent with work showing increased levels of PC2 in rat kidneys with AKI^31,35. We then tested whether this increase was occurring transcriptionally by measuring the mRNA levels of Pkd2 in nephrectomy control and AKI kidneys. We found that the kidneys afflicted with AKI had significantly higher levels of Pkd2 mRNA (Fig. 1D), indicating that both PC2 transcript and protein are increased with stress. To confirm the translational relevance of this response in humans, we performed immunofluorescent staining for PC2, collecting ducts (staining for the lectin Dolichos biflorus agglutinin [DBA]), and mitochondria (staining for the voltage-dependent anion channel [VDAC]) in normal human kidneys (NHK) or kidneys from patients diagnosed with acute tubular injury (AKI; Figs. 1E, S1D; patient information included in Table S1). Quantification of PC2 intensity per cell area revealed that, as in the murine response to AKI, PC2 was significantly increased in human kidney tubules with AKI (Fig. S1E).

PC2 is increased in livers with non-alcoholic fatty liver disease

Whereas kidney cyst development with ADPKD is well-established, pathologies caused by mutations to PKD2 do not exclusively affect the kidneys. The development of cysts arising from hepatic epithelial cells is a common extrarenal result of ADPKD²⁴. Like cystic kidney cells, PC2-null cystic liver cells exhibit altered intracellular Ca²⁺ handling and changes in intracellular signaling pathways, indicating the importance of PC2 in tissues outside of the kidney⁴³. To investigate whether PC2 abundance also changes in liver cells with stress, we fed mice a normal diet (ND) as control, or high-fat diet (HFD) to induce insulin resistance and hepatic stress⁴⁴. After 8 weeks, mice were subjected to glucose tolerance tests, and the HFD-fed mice were found to be glucose intolerant compared to ND-fed mice (Fig. 2A,B). Livers from these mice were collected and showed increased levels of 4-HNE and C/EBP Homologous Protein (CHOP; Figs. 2C, S2A,B), indicating the induction of stress in HFD-fed mice. Immunoblotting for PC2 showed a significant increase in stressed livers from HFD-fed mice (Figs. 2C, S2C). Additionally, qPCR analysis of liver mRNA from mice fed ND or HFD showed a significant increase in Pkd2 mRNA in the HFD-fed mouse livers (Fig. 2D), demonstrating that stress-related Pkd2 up-regulation is not restricted to renal tissue.

The translational relevance of these findings was verified by performing immunofluorescent staining of normal human livers (NHL) and livers from patients with diet-induced non-alcoholic steatohepatitis (NASH; Figs. 2E, S2D; patient information included in Table S2). Quantification of PC2 fluorescence per cell area demonstrated that human livers afflicted with non-alcoholic fatty liver disease (NAFLD) likewise have increased abundance of PC2 (Fig. 2F), supporting the hypothesis that PC2 retains critical function in tissues beyond the kidney.

PC2 is up-regulated with stress in cardiac tissue

Although the most striking symptom of ADPKD is the formation of bilateral renal cysts, the most common cause of death in ADPKD patients is a consequence of cardiac abnormalities^45,46. Due to the expression of PC2 in cardiac tissue and the apparent importance of the polycystins in heart function, PC2 levels were examined in a murine model of cardiomyopathy and were found to be increased in isoproterenol (ISO)-treated hearts compared to healthy controls³⁶. We observed that cellular stress was induced in the hearts of these ISO-treated mice as indicated by increased 4-HNE levels (Fig. S3A,B), confirming that, as in kidney and liver tissue, increased PC2 was accompanied by cellular stress in the ISO-treated hearts. To test whether PC2 was also transcriptionally up-regulated in the hearts of stressed mice, we compared mRNA levels of Pkd2 in left ventricular (LV) tissue samples from control (sham-operated) and stressed (subjected to transverse aortic constriction [TAC]) mice⁴⁷. Unlike the ISO-treated mice, TAC mice develop cardiac hypertrophy induced by a physical rather than chemical stressor. Compared to sham-operated mice, LV samples from TAC mice showed an increase in Pkd2 mRNA (Fig. S3C), confirming that PC2 is up-regulated transcriptionally in stressed mouse hearts using multiple methods of stress induction.

To determine whether up-regulation of PC2 with stress is conserved in human disease, we compared levels of PC2 in left ventricular (LV) tissue samples from non-failing (NF) human hearts and LV samples of failing human hearts, obtained from patients with ischemic cardiomyopathy (ICM) or non-ischemic cardiomyopathy (NICM; patient information included in Table S3)⁴⁸. PC2 was largely increased in the LV samples of ICM and NICM versus NF hearts (Figs. 3A, S3D), and levels of 4-HNE and CHOP were significantly increased in NICM hearts and trending toward increased in ICM samples (Fig. S3E,F). However, because these stress markers were not significantly increased in ICM samples, we questioned whether the up-regulation of PC2 correlated to the degree of stress in these heart samples. We therefore plotted the relative protein levels of PC2 versus CHOP and found a significant correlation between the expression of these proteins (Fig. 3B), demonstrating that although statistical analyses of 4-HNE and CHOP levels do not show a significant increase in ICM samples, the degree of stress in the heart directly correlates with levels of PC2. Plotting relative PC2 versus 4-HNE levels showed a trend toward correlation, but this was not statistically significant due to an outlier in the NICM group (Fig. S3G).

To test if the increased PC2 seen in NICM and ICM LV tissues was due to differential gene expression, we compared the mRNA levels of PKD2 in these samples versus NF LV samples. Transcript levels of PKD2 were elevated in LV samples from ICM and NICM patients (Fig. 3C), indicating that PC2 increase with stress occurs via transcriptional up-regulation in human hearts. To see if there were differences in cellular stress levels associated with increased PKD2 in the ICM and NICM failing hearts, curated lists of genes associated with cellular responses to ER and oxidative stress were collected from MetaCore (Clarivate Analytics) and Ingenuity Pathway Analysis (Ingenuity Systems, QIAGEN Bioinformatics). Genes from these lists were compiled (Tables S4 and 5, “Compiled”) and used to generate an expression heat map of NF, ICM, and NICM transcripts. All transcripts depicted in the heat map are significantly (p < 0.05) changed among the samples. Transcripts were sorted via hierarchical clustering and demonstrate distinct differential expression patterns in the stress genes of NF compared to ICM and NICM samples (Fig. 3D), demonstrating that up-regulation of PKD2 correlates with altered stress response genes in human hearts.

Because elevated PC2 was associated with increases in canonical markers of both ER (CHOP) and oxidative (4-HNE) stress (Figs. 1A,B, 2C, Fig. S2A,B, Fig. 3A,B, and Fig. S3D–F), we hypothesized that PKD2 expression was changed as part of the integrated stress response (ISR) pathway, an essential adaptive pathway that is activated in response to both ER and oxidative stressors^{49,50,51,52,53}. To explore this idea, we cross-referenced the compiled ER and oxidative stress gene lists to develop a more stringent list of stress-associated genes (Tables S4 and 5, “Overlapping”), and cross-referenced these overlapping lists to identify genes involved in both responses. Between 11 ER stress- and 32 oxidative stress-associated genes, there were 6 genes present in both groups (Fig. 3E), two of which were differentially expressed in the NF versus ICM and NICM heart samples (Fig. S3H,I). We then used correlation analysis with a cutoff of 70% correlation or higher and discovered that one of the ISR genes, NFE2L2, positively correlated with PKD2 expression (Fig. 3F; correlation = 79.2%). NFE2L2, also known as Nrf2, is a transcription factor that binds the antioxidant response element (ARE) and activates the expression of genes involved in the response to cellular insults^54,55,56,57. The other ISR gene that was changed in ICM and NICM samples, ATP2A2, did not pass the 70% correlation cutoff (Fig. S3J). We tested whether these correlations were conserved in the LV from stressed mouse hearts and discovered that, like the human hearts, stressed TAC mice had decreased levels of Atp2a2 (Fig. S3K) and a trend toward increased Nfe2l2 (Fig. S3L). These data suggest that, unlike other stress response proteins, PKD2 up-regulation is non-promiscuous and thus is directly associated with specific ISR pathways.

To then investigate whether PC2 expression increases as a direct consequence of cellular stress, we treated human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) with increasing concentrations of hydrogen peroxide (H₂O₂) to induce cell stress in vitro. H₂O₂ treatment led to increased levels of oxidative stress in iPSC-CMs as measured by 4-HNE (Figs. 3G, S3M). Immunoblotting for PC2 levels in iPSC-CMs showed two distinct bands, as has been previously observed⁵⁸. It is thought that the higher band depicts the full-length, N-glycosylated form of PC2, with the lower band depicting a potentially cleaved, inactive form of PC2. Quantification of full-length PC2 levels showed an increase after 2 hours of H₂O₂ treatment in iPSC-CMs, establishing that increased PC2 occurs as a direct consequence of cellular insult (Fig. 3G,H).

PC2 expression is increased in stressed brains

Having determined that PC2 abundance changes with stress in tissues known to rely on PC2 for proper function, we questioned whether its role as a stress-sensitive protein was conserved in tissues less studied in the context of PC2. Expression of PC2 in the brain led us to test whether its abundance is also altered with stress in the central nervous system. As a model of pathologically altered Ca²⁺ signaling and cell stress in the brain^59,60, we used kainic acid to induce acute seizures in mice⁶¹. Systemic injections of kainate cause epileptiform seizures in the hippocampus and induce hippocampus-restricted neuropathology comparable to that seen in patients with temporal lobe epilepsy⁶¹. Mice were injected intraperitoneally with saline (Sal) or kainic acid (KA; Fig. S4A), and their seizures scored according to a modified Racine scale every 10 minutes for 120 minutes (Fig. 4A, Table S6). Hippocampal lysates collected from randomly-paired, weight- and age-matched mice were found to have increased expression of PC2 in epileptic compared to saline-treated brains (Fig. 4B). Pkd2 and Nfe2l2 mRNA expression was likewise tested from hippocampi of saline- and KA-treated mice and found to be significantly increased with KA induction of epileptic seizures (Figs. 4C, S4B).

We then determined whether this increase was translatable to human disease by investigating if PC2 expression correlates with stress in human brains. Using the RNA-Seq dataset provided by the Allen Institute Ivy Glioblastoma Atlas Project⁶², we examined PKD2 expression in 3 different glioblastoma structures (hyperplastic blood vessels, microvascular proliferation, and leading edge; patient information included in Table S7). Leading edge (LE) samples showed relatively low amounts of PKD2 expression, whereas hyperplastic blood vessels (HBV) and microvascular proliferation (MVP) samples expressed relatively high amounts of PKD2 (Fig. 4D). These findings correlated with differential expression of the ISR genes NFE2L2 and ATP2A2 in the different glioblastoma structures (Fig. S4C,D), indicating altered ISR levels amongst these structures. We then used correlation analysis (correlation ≥ 70%) and found that, like in human hearts, PKD2 levels positively correlated with NFE2L2 in human brains (Fig. 4E; correlation = 76.8%), but not with ATP2A2 (Fig. S4E).

PC2 up-regulation protects cells against stress-induced cell death

Although we determined that PC2 expression is up-regulated as a consequence of cellular insult in multiple tissue types, whether this increase is detrimental or favorable for the cell remained unclear. To test this, we utilized a kidney epithelial cell line (LLC-PK1) with wild-type levels of PC2 (WT) or PC2 knocked down (PC2 KD; Fig. S5A) to assess PC2’s role in the cellular stress response. Cells were serum-starved (SS) to induce stress (Fig. S5A,B)^63,64,65 and, consistent with our findings in animal and human tissues, cells showed increased PC2 mRNA and protein expression following serum starvation (Fig. 5A–C, S5A,C) and treatment with tunicamycin (TM), an inducer of ER stress (Fig. S5D–F). We then measured cell viability of WT and PC2 KD cells under basal and stressed conditions. When stress was induced through serum starvation or with TM treatment, PC2 KD cells showed decreased cell viability compared to WT cells (Figs. 5D, S5G), consistent with previous work showing that loss of PC2 renders kidney cells hyper-sensitive to stress³¹, and indicating that up-regulation of PC2 occurs as a protective mechanism. To test our hypothesis that PC2 up-regulation protects against cell stress by enhancing intracellular Ca²⁺ signaling, we measured cell viability in serum-starved cells treated concurrently with the intracellular Ca²⁺ chelator BAPTA-AM. When Ca²⁺ signaling was blunted in SS WT cells through BAPTA-AM treatment, cell viability decreased to levels of SS PC2 KD cells (Fig. 5D). However, in SS KD cells treated with BAPTA-AM, there was no further decrease in cell viability (Figs. 5D, S5H), indicating that a PC2-dependent Ca²⁺ response plays a significant role in the cells’ ability to combat stress. Finally, we measured the degree of stress-induced apoptosis through immunofluorescence and western blot analyses of cleaved caspase-3 activation and found that, compared to WT cells, PC2 KD cells had increased levels of apoptosis when stressed (Figs. 5CE,F, S5A,D,I). The same results were observed when testing another cell line (mIMCD-3) containing normal levels of PC2 (WT) or with PC2 knocked out via CRISPR/Cas9 (PC2 KO; Fig. S5J–L). These data demonstrate that PC2 up-regulation serves to protect cells against stress, and that with inadequate levels of PC2, cells are rendered hyper-susceptible to stress-induced cell death.

Discussion

In this study, we establish that PC2 is a stress-responsive protein whose expression is elevated in a variety of cell types under multiple pathological conditions. Its up-regulation is a direct consequence of ER and oxidative stress, and its mRNA expression significantly correlates with Nfe2l2, a transcription factor that is part of the ISR pathway⁶⁶. Loss of PC2 resulted in a Ca²⁺-mediated decrease in cell viability in response to stress and increased levels of stress-induced apoptosis. Collectively, these findings demonstrate that PC2 plays an important role in general cell homeostasis in numerous tissue types, and that up-regulation of PC2 helps protect cells against stress-induced cell death under pathological conditions.

The importance of PC2 in the maintenance of cellular homeostasis is well-supported by the pathological dysfunctions that occur in cystic ADPKD cells. Our findings indicate that PC2 is increased transcriptionally with cell stress, and that this occurs in response to specific signaling pathways. The function of PC2 as a modulator of Ca²⁺ signaling fits well with these findings, as Ca²⁺ mobilization is a critical step in the cell’s ability to respond to and protect against pathological stressors. As our data indicate, enhanced Ca²⁺ signaling facilitated by PC2 following cell stress contributes significantly to the cell’s adaptive response, whereas blunted Ca²⁺ through intracellular chelation or the absence of PC2 causes hypersensitivity of the cells to outside stressors. Though changes in PC2 levels have been noted in different pathological conditions, the causes for its differential expression after development remained incompletely explored. In support of our findings, previous studies have shown that both Pkd2 transcript and protein levels are increased in kidneys following ischemia/reperfusion injury, and that mice with decreased levels of PC2 are more sensitive to injury in both kidney and smooth muscle cells^31,67,68,69. The correlation we discovered between PKD2 and NFE2L2 levels suggests that PKD2 may be up-regulated via Nrf2, a transcription factor that is increased following cellular insults including oxidative stress⁷⁰. Much of what is known regarding the transcriptional regulation of Pkd2 is based upon its cis-acting promoter region, which contains putative binding sites for developmentally-regulated transcription factors such as Sp1, NF-1, and AP-2^71,72. However, trans-regulatory effects on Pkd2 expression have not been described and may contain additional regulatory elements to alter PC2 levels.

Our results demonstrate that PC2 KD and KO renders cells susceptible to stress-induced death. It therefore logically follows that cystic cells characterized by loss the of PC2 would exhibit decreased cell viability in response to stress. In support of this, a standard phenotype associated with ADPKD is enhanced apoptosis during cyst development^69,73,74, where cellular stress levels are high due to many pathological factors, including renal ischemia and altered cell metabolism. In fact, treatment of ADPKD mice with caspase inhibitors (inhibitors of apoptosis) results in decreased cyst volume and cell proliferation⁷⁴. Additionally, PC2 haploinsufficient (Pkd2^+/-) kidney cells that express decreased overall levels of PC2 show hypersensitivity to cell stress. Pkd2^+/- mice develop larger, more pronounced kidney cysts when treated with Tumor Necrosis Factor alpha (TNFα, an inflammatory cytokine) to induce stress as compared to wild-type littermates, whereas treatment of Pkd2^+/- mice with TNFα inhibitor blocked cyst formation⁷⁵. Additional studies seeking effective treatment for kidney disease have identified resveratrol, a potent activator of Nrf2⁷⁶, as a potentially compelling therapeutic agent for slowing cyst progression in ADPKD^77,78. Whereas these studies have focused on the effects of resveratrol in ameliorating the inflammatory response associated with cyst development, it is possible that resveratrol may act through Nrf2 to help restore normal ISR activity in these cells as well.

Although renal cyst formation and kidney failure are arguably the most well-known symptoms of PC2 dysfunction, multiple extrarenal pathologies are also known to occur in patients with loss-of-function PKD2 mutations. Indeed, ADPKD patients commonly present with numerous manifestations of the disease, including colonic diverticula^79,80, hernia^81,82, cerebral aneurisms⁸³, and the development of hepatic⁸⁴, pancreatic²⁵, and seminal vesicle^85,86 cysts. Most notably, however, rather than renal failure, the major cause of death in patients with ADPKD is due to cardiac dysfunction⁸³. Studies seeking to elucidate how the loss of PC2 affects the heart have shown that with increased age, decreased PC2 levels result in cardiac dysfunction independent of renal abnormalities⁸⁷. Additionally, in agreement with our findings, PC2 levels are enhanced in cardiomyocytes with cardiac injury, and Pkd2^+/- mice show a diminished capacity to recover from injury following the cessation of stress³⁶. It has been suggested that the extrarenal manifestations seen in ADPKD patients are merely secondary effects caused by the main pathology of renal cysts. However, our findings highlight the importance of PC2 as a ubiquitous protein essential for proper cell function not only in the kidney, but in all tissue types. Based on this, the role of PC2 in numerous Ca²⁺-associated stress pathologies may prove to be a promising target by which to restore normal Ca²⁺ and/or ISR homeostasis.

Our in vitro data suggest that PC2 regulation of Ca²⁺ signaling is required to maintain cell viability in the face of stress. Whereas the function of PC2 as a Ca²⁺-permeable cation channel is well-established, there currently exists controversy over where PC2 exerts its intrinsic channel function. It is thought that due to the ER retention signal within its C-terminal tail, the majority of PC2 is located on the ER^5,88, with the rest being localized to the primary cilia in association with PC1⁸⁹ or TRPV4⁹⁰, where it exerts its anti-cystogenic function⁹¹. However, others have suggested that PC2 is also present and functions as a Ca²⁺ channel on the plasma membrane^92,93. In the context of our findings, we believe that PC2 exerts its stress response function from its localization on the ER based upon (1) immunofluorescent imaging demonstrating that PC2 localization remains intracellular, even under stressed conditions (Figs. S1D and S2D) and (2) the up-regulation of PC2 with stress in terminally-differentiated neurons and cardiomyocytes, whose cilia are stumpy, essentially vestigial organelles. Nevertheless, the localization of PC2 does not ultimately influence the findings of this manuscript, as PC2 is believed to facilitate enhanced cytoplasmic Ca²⁺ signaling whether functioning on the ER, primary cilia, or plasma membrane.

Additionally, though PC2 is itself can form a Ca²⁺-permeable cation channel, it is known to interact with other cation channels to enhance intracellular Ca²⁺ signaling (including the inositol 1,4,5-trisphosphate receptor^39,40,94, ryanodine receptor⁹⁵, and other TRP channels^90,96). Therefore, whether PC2 is altering intracellular Ca²⁺ signaling through its intrinsic channel activity or through interactions with other channels remains unclear. Interestingly, PC2 channel activity has been shown to be sensitive to H₂O₂, whose treatment caused an up-regulation of PC2 in human iPSC-CMs. Because the reported IC₅₀ of this inhibition is ~193 μM⁹⁷, we do not believe that the H₂O₂ concentration used in our experiment (up to 200 μM) would be sufficient to completely eliminate a Ca²⁺ current through PC2. Nonetheless, if it were the case that PC2 is fully inhibited with stress, our data showing that BAPTA-AM treatment (Fig. 5D) in PC2 KD cells has no effect on cell viability compared to WT cells demonstrates the requirement for PC2-mediated Ca²⁺ signaling in the response to cell stress, whether this is through PC2’s intrinsic channel activity or its interactions with other channels.

Our study is limited by the variability of sample size throughout the different types of tissues and stress. For all conditions, we tested at least n = 3 samples to ensure that proper statistics could be performed during analyses. When possible, we maximized the sample size to increase the power of our study. However, the sample size of human and mouse tissues varied depending upon availability. Variables affecting this included limited access to human pathological samples with specific diagnoses, and the survival of mice undergoing stress procedures. Additionally, though our data point to a potential link between PKD2 and NFE2L2 expression, we do not presume to state that NFE2L2 directly causes PKD2 up-regulation based on our results. Rather, our data show that PKD2 expression correlates with the activation of the ISR pathway due to its role as a stress response protein. The possibility remains that 1) increased Nrf2 may influence PKD2 expression directly, 2) NFE2L2 transcription may be increased due to altered signaling in cells with increased PC2, 3) PKD2 and NFE2L2 are up-regulated under similar stress conditions, but neither one directly affects the expression of the other, or 4) increased PKD2 mRNA is independent of its transcription, but rather is a consequence of post-transcriptional changes such as mRNA stability. Consequently, if and how PC2 and Nrf2 influence one another’s expression, along with the exact mechanism of increased PKD2 transcript will require further in-depth mechanistic studies.

Collectively, we describe a new functional role for PC2 as a stress-sensitive protein that is up-regulated in response to cellular insults in multiple disease states and tissue types. Moreover, loss of PC2 is sufficient to render cells hypersusceptible to stress-induced cell death, implicating altered stress response pathways in the development of polycystin-related pathologies. The ubiquitous expression of PC2 throughout the body raises the possibility that PC2 may contribute to disease states in other tissues where the ISR is induced or disrupted, and may provide a novel target to help ameliorate the progression of these diseases.

Materials and Methods

Reagents and antibodies

Anti-PC2 (sc-47734; for immunoblotting), anti-NFκB (sc-8008), and anti-IκBα (sc-1643) antibodies were purchased from Santa Cruz Biotechnology. Anti-PC2 antibody for immunofluorescent imaging was a kind gift from Dr. Stefan Somlo (Yale). Mouse anti-beta-Actin (#3700), rabbit anti-beta-Actin (#4970), anti-CHOP (#2895), anti-cleaved caspase-3 (#9664), and anti-GAPDH (#2118) antibodies were purchased from Cell Signaling Technology. Anti-4-Hydroxynonenal (ab48506), anti-eIF2α (ab50733), anti-phospho-eIF2α (ab32157) antibodies, and kainic acid (ab120100) were purchased from Abcam. Anti-VDAC (PA1-954A) antibody was purchased from Thermo Fisher Scientific. Hydrogen peroxide (H325-100) and BAPTA-AM (B1205) were purchased from Thermo Fisher Scientific. Tunicamycin (T7765), and Dimethyl sulfoxide (DMSO; W387520) were purchased from Sigma-Aldrich.

Animal studies

The Yale University and University of Illinois at Urbana-Champaign Institutional Animal Care and Use Committees (IACUC) approved the animal housing conditions and the experimental procedures conducted in this study. All experiments were performed in accordance with relevant guidelines and regulations. C57BL/6 mice were kept under standard laboratory conditions with free access to food and water. Control mice were provided 2018S Teklad global rodent diet (Envigo). For diet-induced obesity, mice were fed TD.06414 Teklad diet containing 60% kcal/fat (Envigo) for 8 weeks-14 months, as described in the figure legends, beginning at 10 weeks of age. All animal experiments were performed in a blinded manner.

Renal ischemia/reperfusion mouse model

Male 8- to 10-week-old C57BL/6 mice (National Institutes of Health/National Cancer Institute) were anesthetized with i.p. ketamine (100 mg/kg) and xylazine (10 mg/kg) then subjected to renal ischemia reperfusion (I/R) using a modified approach of that described previously⁹⁸. Briefly, the right renal pedicle was isolated through a midline abdominal incision and clamped for 27 minutes using a nontraumatic microaneurysm clip (B-2, Fine Science Tools). The left kidney was removed and collected immediately before I/R of the right kidney (Sham, nephrectomized kidney). Mice were kept at 37 °C at all times during the procedure, and reperfusion of kidneys was confirmed after clamp release. Mice were given 1 ml normal saline intraperitoneally to prevent dehydration and were euthanized 72 hours after I/R. Kidney tissue was harvested for immunoblotting as described below.

Glucose tolerance testing

At 18 weeks of age, mice were fasted for 16 hours before glucose tolerance testing. Glucose was administered via i.p. injection (1.5 g/kg body weight). Blood glucose measurements were taken immediately before injection and at 15, 30, 60, and 120 minutes following injection. Blood was collected using a lateral tail nick and glucose levels were measured using blood glucose strips and OneTouch glucometer (LifeScan).

Kainic acid-induced acute seizure mouse model

At 8–10 weeks of age, male C57BL/6 J mice (Jackson Laboratory, Stock Number: 000664) received an i.p. injection of kainic acid (30 mg/kg body weight) or an equal volume of 0.9% saline as described⁹⁹. Mice were returned to their cages and monitored for behavioral seizures every 10 minutes for 2 hours following injection. Behavioral seizures were scored according to a modified Racine scale as described previously^100,101. At 24 hours post injection, mice were euthanized by CO₂ inhalation and brains stored at −80 °C until use.

Brain lysate preparation

The dissected brain regions per mouse were homogenized in ice-cold homogenization buffer (Solution A) containing (in mM): 320 sucrose, 1 NaHCO₃, 1 MgCl₂, 0.5 CaCl₂, 0.4 HEPES (pH 7.4) and Halt protease inhibitors (Thermo Fisher Scientific) as previously described⁹⁹. After centrifuging at 1400 x g for 10 minutes at 4 °C, the homogenate supernatant (S1) was separated from insoluble tissue and nuclear pellet (P1). The S1 fraction was then centrifuged at 13,800 x g for 10 min at 4 °C. The supernatant with cytosolic soluble proteins (S2) was removed, and the remaining pellet with transmembrane proteins and membrane-bound proteins (P2 membrane fraction) was resuspended in ice-cold solution B containing (in mM): 160 sucrose, 6 Tris-HCl, 0.5% Triton-X (pH 8.0) and Halt protease inhibitors. Pierce BCA assay (Thermo Fisher Scientific) was performed to normalize protein concentrations to 1 mg/ml in Solution B (pH 7.4). The S1, S2, and P2 fractions were stored at −80 °C until use.

Western blot

Lysates of mouse kidneys, hearts, livers and human hearts were prepared by homogenization in radioimmunoprecipitation assay (RIPA) buffer containing SDS (Santa Cruz Biotechnology) with Halt protease and phosphatase inhibitor cocktail (Thermo Fisher). Lysates of mouse hippocampi were prepared as described above and the P2 fractions were run for western blotting. Cultured cells were lysed directly in M-PER mammalian protein extraction reagent (Thermo Fisher) supplemented with Halt protease and phosphatase inhibitor cocktail. Equal amounts of protein were loaded, and electrophoresis was performed in NuPAGE 4–12% gradient bis-tris polyacrylamide protein gels (Thermo Fisher). Proteins were transferred to PVDF membrane and blocked with 5% milk in phosphate-buffered saline with Tween-20 for 1 hour. Membranes were then incubated overnight with primary antibody at 4 °C. Blots were washed and incubated with secondary antibody for 1 hour at room temperature. After washing, the secondary antibody was visualized by Pierce ECL chemiluminescence reagents (Thermo Fisher) or using a LI-COR Odyssey imaging system (LI-COR Biosciences).

Human tissue

Human kidney and liver tissues were identified and obtained through the Department of Pathology at the Yale School of Medicine. All experimental protocols and the use of these tissues for research were approved by the Yale Institutional Review Board. All methods were carried out in accordance with relevant guidelines and regulations. Informed consent was obtained from all subjects donating samples. Tissues were fixed with 4% paraformaldehyde at 4 °C overnight, embedded in paraffin, and 5 μm sections were cut for immunofluorescence. Following deparaffinization and rehydration, antigen retrieval was performed by incubating the sections in a steamer for 20 min in sodium citrate buffer (10 mM Tri-sodium citrate, 0.05% Tween-20, pH 6.0). Sections were then quenched of autofluorescence, blocked and permeabilized, and incubated with anti-PC2 (Santa Cruz Biotechnology), anti-lectin Dolichos biflorus agglutinin (DBA; Vector Laboratories), and anti-VDAC (Cell Signaling) antibodies. Tissues were mounted in ProLong Gold Antifade Mountant (Life Technologies) and imaged with 40× and 100× oil-immersion lenses on a Leica SP8 gated STED Microscope using Leica LAS X software (Heidelberg, Germany). To enable comparison among samples, the same laser power, gain and acquisition settings were used across all slides.

Immunofluorescence

LLC-PK1 and mIMCD3 cells were immunostained as described previously⁴¹. Briefly, cells were plated on poly-L-lysine-coated glass coverslips and fixed with 4% paraformaldehyde for 10 minutes at 37 °C. After blocking in 2% BSA and 0.2% Triton X-100, cells were incubated in the same solution with primary antibody for active caspase 3 and PC2 overnight at 4 °C, then incubated in anti-rabbit AlexaFluor 488 (Life Technologies), phalloidin conjugated to tetramethylrhodamine (TRITC; Life Technologies), and anti-mouse AlexaFluor 633 (Life Technologies) for 1 hour before mounting with ProLong Gold antifade mounting reagent with DAPI (Life Technologies). Slides were imaged with a Leica TCS SP5 Confocal Laser Scanning Microscope.

To calculate PC2 and Cleaved Caspase 3 intensity, ImageJ (NIH) was used for image processing. All measurements of fluorescence intensity were calculated using images taken at 10X magnification to ensure unbiased and robust quantification. Individual cells or cell groups were selected as regions of interest (ROIs,) and the fluorescence intensity and area were calculated for each ROI. Intensity was divided by its corresponding area and averaged across each image. Five images were taken per condition and averaged to plot as Intensity/Area.

Human heart RNA-Seq

RNA Sequencing was performed on left ventricular tissue samples from non-failing (NF; n = 8) human donor hearts, and from failing human hearts obtained from patients with ischemic cardiomyopathy (ICM; n = 8) or non-ischemic cardiomyopathy (NICM; n = 8) as described previously⁴⁸. Data were analyzed using Qlucore Omics Explorer (Lund, Sweden). Normalized Reads Per Kilobase of transcript, per Million mapped reads (RPKM) values were log₂ transformed and fold change calculated. Curated lists of genes associated with cellular responses to ER and oxidative stress were collected and cross-referenced from MetaCore (Clarivate Analytics) and Ingenuity Pathway Analysis (Ingenuity Systems, QIAGEN Bioinformatics). The genes were compiled and used to generate an expression heat map of differentially regulated (p < 0.05) ER and oxidative stress-related genes. Linear regression analysis was performed to show significant (p < 0.0001) correlation between PKD2 and NFE2L2 transcripts.

iPSC culture and differentiation

Human induced pluripotent stem cells (iPSC) were acquired from the Coriell Institute (GM23338), as characterized previously¹⁰². iPSC colonies were maintained on growth-factor reduced Matrigel (Corning)-coated tissue culture plates in mTeSR1 medium (Stem Cell Technologies). iPSCs were differentiated into iPSC-derived cardiomyocytes (iPSC-CMs) following a sequential protocol of manipulating the WNT pathway¹⁰³, using 12.5 μM CHIR99021 (Stem Cell Technologies) for 24 hours and 5 μM IWP4 (Tocris Bioscience) for 48 hours on day 3 after the induction of differentiation. Subsequently, the differentiating cultures were maintained in RPMI + B2-insulin until day 11 when spontaneous beating was observed. Media was then changed to RPMI + B27 + insulin for 2 days, followed by 4 days of metabolic selection using DMEM without glucose and 4 mM lactate¹⁰⁴. iPSC-CMs were kept in RPMI + B27 + insulin until day 21 after the start of differentiation when they were dissociated and re-plated on a 12-well plate coated with 50 μg/ml fibronectin (bovine, Sigma-Aldrich)¹⁰⁵. iPSC-CMs were cultured for a subsequent 2 days in RPMI + B27 + insulin before experiments were performed.

Human glioblastoma project RNA-Seq

The open-source RNA-Seq dataset from The Allen Institute’s human glioblastoma project was used to interrogate the relationship between PKD2 expression in human brain and integrated stress response genes. RNA-Seq was performed on different glioblastoma structures as described⁶² and the FPKM values log₂ normalized before analysis with Qlucore Omics Explorer. Linear regression analysis was performed to show significant (p < 0.0001) correlation between PKD2 and NFE2L2 transcripts.

Creation of stable knockdown cells

Short hairpin RNA (shRNA) against Pkd2 was designed to be specific to the pig sequence. The previously described^41,106 PC2 shRNA constructs were put into a psiRNA vector (InvivoGen, San Diego, CA), which was stably transfected into LLC-PK1 cells. Cells were exposed to G418 (2.5 mg/ml) as previously described^41,106. LLC-PK1 cells were maintained in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and kept at 37 C in 5% CO₂.

In vitro stress treatment

Cells were plated on a 6-well plate (Corning) at a density of 400,000 cells per well. The following day, cells were either treated with the commonly used ER-stress inducer Tunicamycin (TM)¹⁰⁷ or serum-starved for 24 hours. After treatment, the cells were lysed and collected as described above for Western Blot or stained for Immunofluorescence.

Measurement of cellular stress

To assess the level of cellular stress in both in vivo and in vitro samples, we immunoblotted for several markers whose levels are changed in response to stress: 4-HNE, a reactive short-chain aldehyde formed during lipid peroxidation following oxidative stress¹⁰⁸; CHOP, a protein involved in ER-stress mediated apoptosis⁵¹; eIF2α, whose phosphorylation (p-EIF2α) is the core event in the integrated stress response pathway⁵⁰; cleaved caspase 3, a commonly used marker for apoptotic cells¹⁰⁹.

mRNA analysis

mRNA was extracted from animal tissue and cultured cells using a RNeasy RNA Isolation Kit (Qiagen, Hilden, Germany) and reverse-transcribed to complementary DNA (cDNA) using Multiscribe Reverse Transcriptase and random primers (Applied Biosystems, Foster City, CA). For real-time quantitative PCR, 20 ng of cDNA was used as transcript template in a reaction with Power SYBR Green Master Mix (Applied Biosystems) on a 7500 Fast Real-Time PCR system (Applied Biosystems). Fold change in Pkd2 (Fwd 5′—CAGAGGGGCTGCTACAGTTT—3′; Rev 5′—TTGAAGAGCTTAATCCAGACCA—3′) and Nfe2l2 (Fwd 5′—AGATGACCATGAGTCGCTTGC—3′; Rev 5′—CCTGATGAGGGGCAGTGAAG—3′) mRNA transcript levels compared to control samples were determined using the 2^−(ΔΔCT) method. Actin (Fwd 5′—GTGACGTTGACATCCGTAAAGA—3′; Rev 5′—GCCGGACTCATCGTACTCC—3′) or Gapdh (Fwd 5′—AGGTCGGTGTGAACGGATTTG—3′; Rev 5′—GGGGTCGTTGATGGCAACA—3′) were used as internal control.

CellTiter-Glo assay

Cells were plated at a density of 1000 cells per well on a 96-well plate (Corning) and treated the following day. After 24 hours of treatment, CellTiter-Glo Luminescent Cell Viability assays were carried out according to the manufacturer’s instructions (Promega Corporation). Experiments were performed in triplicates with 10 replicates per experiment.

Statistical analysis

For cell-based experiments, data were calculated from at least three separate preparations. For animal-based experiments, data were calculated from at least three biological replicates. Where appropriate, one-way analysis of variance (ANOVA) with multiple comparisons or non-parametric Mann Whitney U test was applied. Data are presented as (1) mean ± SD, or (2) median with range, as stated in the figure legend. In all experiments, p < 0.05 was considered statistically significant. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.

Data availability

The data generated, used, and/or analyzed in the current study are available from the corresponding author upon reasonable request.

References

Cornec-Le Gall, E. et al. PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis. American Journal of Kidney Diseases 70, 476–485, https://doi.org/10.1053/j.ajkd.2017.01.046 (2017).
Article CAS PubMed Google Scholar
Uhlen, M. et al. Towards a knowledge-based Human Protein Atlas. Nature biotechnology 28, 1248–1250, https://doi.org/10.1038/nbt1210-1248 (2010).
Article CAS PubMed Google Scholar
Uhlen, M. et al. Proteomics. Tissue-based map of the human proteome. Science (New York, N.Y.) 347, 1260419, https://doi.org/10.1126/science.1260419 (2015).
Article CAS Google Scholar
Thul, P. J. et al. A subcellular map of the human proteome. Science (New York, N.Y.) 356, https://doi.org/10.1126/science.aal3321 (2017).
Article Google Scholar
Koulen, P. et al. Polycystin-2 is an intracellular calcium release channel. Nature Cell Biology 4, 191–197, https://doi.org/10.1038/ncb754 (2002).
Article CAS PubMed Google Scholar
Cantiello, H. F. Regulation of calcium signaling by polycystin-2. American journal of physiology. Renal physiology 286, F1012–1029, https://doi.org/10.1152/ajprenal.00181.2003 (2004).
Article CAS PubMed Google Scholar
Anyatonwu, G. I. & Ehrlich, B. E. Calcium signaling and polycystin-2. Biochemical and Biophysical Research Communications 322, 1364–1373, https://doi.org/10.1016/j.bbrc.2004.08.043 (2004).
Article CAS PubMed Google Scholar
Hofer, A. M. Interactions between calcium and cAMP signaling. Current medicinal chemistry 19, 5768–5773 (2012).
Article CAS Google Scholar
Torres, V. E. & Harris, P. C. Strategies targeting cAMP signaling in the treatment of polycystic kidney disease. Journal of the American Society of Nephrology: JASN 25, 18–32, https://doi.org/10.1681/asn.2013040398 (2014).
Article CAS PubMed Google Scholar
Padovano, V. et al. The polycystins are modulated by cellular oxygen-sensing pathways and regulate mitochondrial function. Mol Biol Cell 28, 261–269, https://doi.org/10.1091/mbc.E16-08-0597 (2017).
Article CAS PubMed PubMed Central Google Scholar
Kuo, I. Y. et al. Polycystin 2 regulates mitochondrial Ca<sup>2 + </sup> signaling, bioenergetics, and dynamics through mitofusin 2. Science signaling 12, eaat7397, https://doi.org/10.1126/scisignal.aat7397 (2019).
Article CAS PubMed PubMed Central Google Scholar
Goilav, B. Apoptosis in polycystic kidney disease. Biochimica et biophysica acta 1812, 1272–1280, https://doi.org/10.1016/j.bbadis.2011.01.006 (2011).
Article CAS PubMed Google Scholar
Wegierski, T. et al. TRPP2 channels regulate apoptosis through the Ca2 + concentration in the endoplasmic reticulum. The EMBO journal 28, 490–499, https://doi.org/10.1038/emboj.2008.307 (2009).
Article CAS PubMed PubMed Central Google Scholar
Grantham, J. J. Lillian Jean Kaplan International Prize for advancement in the understanding of polycystic kidney disease. Understanding polycystic kidney disease: a systems biology approach. Kidney international 64, 1157–1162, https://doi.org/10.1046/j.1523-1755.2003.00242.x (2003).
Article PubMed Google Scholar
Calvet, J. P. Strategies to Inhibit Cyst Formation in ADPKD. Clinical Journal of the American Society of Nephrology 3, 1205, https://doi.org/10.2215/CJN.05651207 (2008).
Article PubMed Google Scholar
Rowe, I. et al. Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy. Nature medicine 19, 488–493, https://doi.org/10.1038/nm.3092 (2013).
Article CAS PubMed PubMed Central Google Scholar
Riwanto, M. et al. Inhibition of Aerobic Glycolysis Attenuates Disease Progression in Polycystic Kidney Disease. PloS one 11, e0146654, https://doi.org/10.1371/journal.pone.0146654 (2016).
Article CAS PubMed PubMed Central Google Scholar
Menezes, L. F., Lin, C. C., Zhou, F. & Germino, G. G. Fatty Acid Oxidation is Impaired in An Orthologous Mouse Model of Autosomal Dominant Polycystic Kidney Disease. EBioMedicine 5, 183–192, https://doi.org/10.1016/j.ebiom.2016.01.027 (2016).
Article PubMed PubMed Central Google Scholar
Roveri, A. et al. Effect of hydrogen peroxide on calcium homeostasis in smooth muscle cells. Archives of Biochemistry and Biophysics 297, 265–270, https://doi.org/10.1016/0003-9861(92)90671-I (1992).
Article CAS PubMed Google Scholar
Renard, D. C., Seitz, M. B. & Thomas, A. P. Oxidized glutathione causes sensitization of calcium release to inositol 1,4,5-trisphosphate in permeabilized hepatocytes. Biochemical Journal 284, 507, https://doi.org/10.1042/bj2840507 (1992).
Article CAS PubMed PubMed Central Google Scholar
Rooney, T. A., Renard, D. C., Sass, E. J. & Thomas, A. P. Oscillatory cytosolic calcium waves independent of stimulated inositol 1,4,5-trisphosphate formation in hepatocytes. Journal of Biological Chemistry 266, 12272–12282 (1991).
CAS PubMed Google Scholar
Wang, H. & Joseph, J. A. Mechanisms of hydrogen peroxide-induced calcium dysregulation in PC12 cells. Free Radical Biology and Medicine 28, 1222–1231, https://doi.org/10.1016/S0891-5849(00)00241-0 (2000).
Article CAS PubMed Google Scholar
Ermak, G. & Davies, K. J. Calcium and oxidative stress: from cell signaling to cell death. Molecular immunology 38, 713–721 (2002).
Article CAS Google Scholar
Chauveau, D., Fakhouri, F. & GrÜNfeld, J.-P. Liver Involvement in Autosomal-Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology 11, 1767 (2000).
CAS PubMed Google Scholar
Kim, J. A. et al. Pancreatic Cysts in Autosomal Dominant Polycystic Kidney Disease: Prevalence and Association with PKD2 Gene Mutations. Radiology 280, 762–770, https://doi.org/10.1148/radiol.2016151650 (2016).
Article PubMed PubMed Central Google Scholar
Chang, M. Y. & Ong, A. C. M. Autosomal Dominant Polycystic Kidney Disease: Recent Advances in Pathogenesis and Treatment. Nephron Physiology 108, p1–p7, https://doi.org/10.1159/000112495 (2008).
Article CAS PubMed Google Scholar
Vlak, M. H., Algra, A., Brandenburg, R. & Rinkel, G. J. Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis. The Lancet. Neurology 10, 626–636, https://doi.org/10.1016/s1474-4422(11)70109-0 (2011).
Article PubMed Google Scholar
Ecder, T. Cardiovascular complications in autosomal dominant polycystic kidney disease. Current hypertension reviews 9, 2–11 (2013).
Article Google Scholar
Yu, T.-M. et al. Risk of cancer in patients with polycystic kidney disease: a propensity-score matched analysis of a nationwide, population-based cohort study. The Lancet Oncology 17, 1419–1425, https://doi.org/10.1016/S1470-2045(16)30250-9 (2016).
Article PubMed Google Scholar
Sun, K., Xu, D. & Mei, C. The association between autosomal dominant polycystic kidney disease and cancer. International urology and nephrology 51, 93–100, https://doi.org/10.1007/s11255-018-1951-5 (2019).
Article CAS PubMed Google Scholar
Prasad, S., McDaid, J. P., Tam, F. W. K., Haylor, J. L. & Ong, A. C. M. Pkd2 Dosage Influences Cellular Repair Responses following Ischemia-Reperfusion Injury. The American Journal of Pathology 175, 1493–1503, https://doi.org/10.2353/ajpath.2009.090227 (2009).
Article CAS PubMed PubMed Central Google Scholar
Pennekamp, P. et al. The ion channel polycystin-2 is required for left-right axis determination in mice. Current biology: CB 12, 938–943 (2002).
Article CAS Google Scholar
Markowitz, G. S. et al. Polycystin-2 expression is developmentally regulated. American Journal of Physiology-Renal Physiology 277, F17–F25, https://doi.org/10.1152/ajprenal.1999.277.1.F17 (1999).
Article CAS Google Scholar
Bisgrove, B. W., Snarr, B. S., Emrazian, A. & Yost, H. J. Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer’s vesicle are required for specification of the zebrafish left-right axis. Developmental biology 287, 274–288, https://doi.org/10.1016/j.ydbio.2005.08.047 (2005).
Article CAS PubMed Google Scholar
Zhao, Y. Polycystin-2 expression is increased following experimental ischaemic renal injury. 17, 2138–2144, https://doi.org/10.1093/ndt/17.12.2138 (2002).
Article CAS Google Scholar
Giehl, E. et al. Polycystin 2-dependent cardio-protective mechanisms revealed by cardiac stress. Pflugers Archiv: European journal of physiology 469, 1507–1517, https://doi.org/10.1007/s00424-017-2042-7 (2017).
Article CAS PubMed Google Scholar
Lu, J. et al. Polycystin-2 Plays an Essential Role in Glucose Starvation-Induced Autophagy in Human Embryonic Stem Cell-Derived Cardiomyocytes. STEM CELLS 36, 501–513, https://doi.org/10.1002/stem.2764 (2018).
Article CAS PubMed Google Scholar
Gargalionis, A. N. et al. Polycystin-1 and polycystin-2 are involved in the acquisition of aggressive phenotypes in colorectal cancer. International Journal of Cancer 136, 1515–1527, https://doi.org/10.1002/ijc.29140 (2015).
Article CAS PubMed Google Scholar
Li, Y., Wright, J. M., Qian, F., Germino, G. G. & Guggino, W. B. Polycystin 2 Interacts with Type I Inositol 1,4,5-Trisphosphate Receptor to Modulate Intracellular Ca2 + Signaling. Journal of Biological Chemistry 280, 41298–41306, https://doi.org/10.1074/jbc.M510082200 (2005).
Article CAS PubMed Google Scholar
Sammels, E. et al. Polycystin-2 activation by inositol 1,4,5-trisphosphate-induced Ca 2 + release requires its direct association with the inositol 1,4,5-trisphosphate receptor in a signaling microdomain. 285, jbc.M109.090662, https://doi.org/10.1074/jbc.m109.090662 (2010).
Article CAS Google Scholar
Kuo, I. Y. et al. Cyst formation following disruption of intracellular calcium signaling. Proceedings of the National Academy of Sciences 111, 14283, https://doi.org/10.1073/pnas.1412323111 (2014).
Article ADS CAS Google Scholar
Young, E. W. & Humes, H. D. Calcium and acute renal failure. Mineral and electrolyte metabolism 17, 106–111 (1991).
CAS PubMed Google Scholar
Spirli, C. et al. Altered store operated calcium entry increases cyclic 3’,5’-adenosine monophosphate production and extracellular signal-regulated kinases 1 and 2 phosphorylation in polycystin-2-defective cholangiocytes. Hepatology (Baltimore, Md.) 55, 856–868, https://doi.org/10.1002/hep.24723 (2012).
Article CAS Google Scholar
Noeman, S. A., Hamooda, H. E. & Baalash, A. A. Biochemical study of oxidative stress markers in the liver, kidney and heart of high fat diet induced obesity in rats. Diabetol Metab Syndr 3, 17–17, https://doi.org/10.1186/1758-5996-3-17 (2011).
Article CAS PubMed PubMed Central Google Scholar
Fick, G. M., Johnson, A. M., Hammond, W. S. & Gabow, P. A. Causes of death in autosomal dominant polycystic kidney disease. Journal of the American Society of Nephrology: JASN 5, 2048–2056 (1995).
CAS PubMed Google Scholar
Orskov, B., Sorensen, V. R., Feldt-Rasmussen, B. & Strandgaard, S. Changes in causes of death and risk of cancer in Danish patients with autosomal dominant polycystic kidney disease and end-stage renal disease. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 27, 1607–1613, https://doi.org/10.1093/ndt/gfr467 (2012).
Article Google Scholar
Yang, K. C., Ku, Y. C., Lovett, M. & Nerbonne, J. M. Combined deep microRNA and mRNA sequencing identifies protective transcriptomal signature of enhanced PI3Kalpha signaling in cardiac hypertrophy. Journal of molecular and cellular cardiology 53, 101–112, https://doi.org/10.1016/j.yjmcc.2012.04.012 (2012).
Article CAS PubMed PubMed Central Google Scholar
Yang, K. C. et al. Deep RNA sequencing reveals dynamic regulation of myocardial noncoding RNAs in failing human heart and remodeling with mechanical circulatory support. Circulation 129, 1009–1021, https://doi.org/10.1161/circulationaha.113.003863 (2014).
Article CAS PubMed PubMed Central Google Scholar
Wang, C. et al. Inhibiting the integrated stress response pathway prevents aberrant chondrocyte differentiation thereby alleviating chondrodysplasia. eLife 7, e37673, https://doi.org/10.7554/eLife.37673 (2018).
Article PubMed PubMed Central Google Scholar
Pakos-Zebrucka, K. et al. The integrated stress response. EMBO Rep 17, 1374–1395, https://doi.org/10.15252/embr.201642195 (2016).
Article CAS PubMed PubMed Central Google Scholar
Harding, H. P. et al. Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells. Molecular Cell 6, 1099–1108, https://doi.org/10.1016/S1097-2765(00)00108-8 (2000).
Article CAS PubMed Google Scholar
Bhandary, B., Marahatta, A., Kim, H.-R. & Chae, H.-J. An involvement of oxidative stress in endoplasmic reticulum stress and its associated diseases. Int J Mol Sci 14, 434–456, https://doi.org/10.3390/ijms14010434 (2012).
Article CAS PubMed PubMed Central Google Scholar
Zeeshan, H. M., Lee, G. H., Kim, H. R. & Chae, H. J. Endoplasmic Reticulum Stress and Associated ROS. Int J Mol Sci 17, 327, https://doi.org/10.3390/ijms17030327 (2016).
Article CAS PubMed PubMed Central Google Scholar
Alam, J. et al. Nrf2, a Cap’n’Collar transcription factor, regulates induction of the heme oxygenase-1 gene. J Biol Chem 274, 26071–26078, https://doi.org/10.1074/jbc.274.37.26071 (1999).
Article CAS PubMed Google Scholar
Kensler, T. W., Wakabayashi, N. & Biswal, S. Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway. Annual review of pharmacology and toxicology 47, 89–116, https://doi.org/10.1146/annurev.pharmtox.46.120604.141046 (2007).
Article CAS PubMed Google Scholar
Kobayashi, A. et al. Oxidative and electrophilic stresses activate Nrf2 through inhibition of ubiquitination activity of Keap1. Molecular and cellular biology 26, 221–229, https://doi.org/10.1128/mcb.26.1.221-229.2006 (2006).
Article CAS PubMed PubMed Central Google Scholar
He, C. H. et al. Identification of Activating Transcription Factor 4 (ATF4) as an Nrf2-interacting Protein: IMPLICATION FOR HEME OXYGENASE-1 GENE REGULATION. Journal of Biological Chemistry 276, 20858–20865, https://doi.org/10.1074/jbc.M101198200 (2001).
Article CAS PubMed Google Scholar
Hofherr, A., Wagner, C., Fedeles, S., Somlo, S. & Köttgen, M. N-glycosylation determines the abundance of the transient receptor potential channel TRPP2. The Journal of biological chemistry 289, 14854–14867, https://doi.org/10.1074/jbc.M114.562264 (2014).
Article CAS PubMed PubMed Central Google Scholar
Gluck, M. R., Jayatilleke, E., Shaw, S., Rowan, A. J. & Haroutunian, V. CNS oxidative stress associated with the kainic acid rodent model of experimental epilepsy. Epilepsy research 39, 63–71 (2000).
Article CAS Google Scholar
Evans, M. C., Griffiths, T. & Meldrum, B. S. Kainic acid seizures and the reversibility of calcium loading in vulnerable neurons in the hippocampus. Neuropathology and applied neurobiology 10, 285–302 (1984).
Article CAS Google Scholar
Ben-Ari, Y. & Cossart, R. Kainate, a double agent that generates seizures: two decades of progress. Trends in neurosciences 23, 580–587 (2000).
Article CAS Google Scholar
Puchalski, R. B. et al. An anatomic transcriptional atlas of human glioblastoma. Science (New York, N.Y.) 360, 660, https://doi.org/10.1126/science.aaf2666 (2018).
Article ADS CAS Google Scholar
Zhang, Y. et al. Tauroursodeoxycholic acid (TUDCA) alleviates endoplasmic reticulum stress of nuclear donor cells under serum starvation. PloS one 13, e0196785, https://doi.org/10.1371/journal.pone.0196785 (2018).
Article CAS PubMed PubMed Central Google Scholar
Zhang, Y. et al. Inhibition of Starvation-Triggered Endoplasmic Reticulum Stress, Autophagy, and Apoptosis in ARPE-19 Cells by Taurine through Modulating the Expression of Calpain-1 and Calpain-2. Int J Mol Sci 18, 2146, https://doi.org/10.3390/ijms18102146 (2017).
Article CAS PubMed Central Google Scholar
Pandey, S., Lopez, C. & Jammu, A. Oxidative stress and activation of proteasome protease during serum deprivation-induced apoptosis in rat hepatoma cells; inhibition of cell death by melatonin. Apoptosis: an international journal on programmed cell death 8, 497–508 (2003).
Article CAS Google Scholar
Teske, B. F. et al. The eIF2 kinase PERK and the integrated stress response facilitate activation of ATF6 during endoplasmic reticulum stress. Molecular biology of the cell 22, 4390–4405, https://doi.org/10.1091/mbc.E11-06-0510 (2011).
Article CAS PubMed PubMed Central Google Scholar
Qian, Q. et al. Pkd2 haploinsufficiency alters intracellular calcium regulation in vascular smooth muscle cells. Human Molecular Genetics 12, 1875–1880, https://doi.org/10.1093/hmg/ddg190 (2003).
Article CAS PubMed Google Scholar
Brookes, Z. L. S. et al. Pkd2 mesenteric vessels exhibit a primary defect in endothelium-dependent vasodilatation restored by rosiglitazone. Am J Physiol Heart Circ Physiol 304, H33–H41, https://doi.org/10.1152/ajpheart.01102.2011 (2013).
Article ADS CAS PubMed Google Scholar
Chang, M. Y. et al. Haploinsufficiency of Pkd2 is associated with increased tubular cell proliferation and interstitial fibrosis in two murine Pkd2 models. Nephrology Dialysis Transplantation 21, 2078–2084, https://doi.org/10.1093/ndt/gfl150 (2006).
Article CAS Google Scholar
Zhang, D. D. Mechanistic Studies of the Nrf2-Keap1 Signaling Pathway. Drug Metabolism Reviews 38, 769–789, https://doi.org/10.1080/03602530600971974 (2006).
Article CAS PubMed Google Scholar
Park, J. H. et al. Cloning and characterization of the murine pkd2 promoter. Genomics 66, 305–312, https://doi.org/10.1006/geno.2000.6197 (2000).
Article CAS PubMed Google Scholar
Rodova, M., Islam, M. R., Maser, R. L. & Calvet, J. P. The polycystic kidney disease-1 promoter is a target of the beta-catenin/T-cell factor pathway. J Biol Chem 277, 29577–29583, https://doi.org/10.1074/jbc.M203570200 (2002).
Article CAS PubMed Google Scholar
Ecder, T. et al. Caspases, Bcl-2 proteins and apoptosis in autosomal-dominant polycystic kidney disease. Kidney international 61, 1220–1230, https://doi.org/10.1046/j.1523-1755.2002.00250.x (2002).
Article CAS PubMed Google Scholar
Edelstein, C. L. What is the role of tubular epithelial cell apoptosis in polycystic kidney disease (PKD)? Cell cycle (Georgetown, Tex.) 4, 1550–1554, https://doi.org/10.4161/cc.4.11.2185 (2005).
Article CAS Google Scholar
Bai, C.-X. et al. Formation of a new receptor-operated channel by heteromeric assembly of TRPP2 and TRPC1 subunits. EMBO reports 9, 472–479, https://doi.org/10.1038/embor.2008.29 (2008).
Article CAS PubMed PubMed Central Google Scholar
Palsamy, P. & Subramanian, S. Resveratrol protects diabetic kidney by attenuating hyperglycemia-mediated oxidative stress and renal inflammatory cytokines via Nrf2-Keap1 signaling. Biochimica et biophysica acta 1812, 719–731, https://doi.org/10.1016/j.bbadis.2011.03.008 (2011).
Article CAS PubMed Google Scholar
Moradi, H. & Vaziri, N. D. Effect of resveratrol on progression of polycystic kidney disease: a case of cautious optimism. Nephrology Dialysis Transplantation 31, 1755–1758, https://doi.org/10.1093/ndt/gfw097 (2016).
Article CAS PubMed Central Google Scholar
Wu, M. et al. Resveratrol delays polycystic kidney disease progression through attenuation of nuclear factor kappaB-induced inflammation. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 31, 1826–1834, https://doi.org/10.1093/ndt/gfw058 (2016).
Article CAS Google Scholar
Scheff, R. T., Zuckerman, G., Harter, H., Delmez, J. & Koehler, R. Diverticular disease in patients with chronic renal failure due to polycystic kidney disease. Annals of internal medicine 92, 202–204, https://doi.org/10.7326/0003-4819-92-2-202 (1980).
Article CAS PubMed Google Scholar
Sharp, C. K., Zeligman, B. E., Johnson, A. M., Duley, I. & Gabow, P. A. Evaluation of colonic diverticular disease in autosomal dominant polycystic kidney disease without end-stage renal disease. American journal of kidney diseases: the official journal of the National Kidney Foundation 34, 863–868, https://doi.org/10.1016/s0272-6386(99)70043-0 (1999).
Article CAS Google Scholar
Morris-Stiff, G., Coles, G., Moore, R., Jurewicz, A. & Lord, R. Abdominal wall hernia in autosomal dominant polycystic kidney disease. The British journal of surgery 84, 615–617 (1997).
Article CAS Google Scholar
Modi, K. B., Grant, A. C., Garret, A. & Rodger, R. S. Indirect inguinal hernia in CAPD patients with polycystic kidney disease. Advances in peritoneal dialysis. Conference on Peritoneal Dialysis 5, 84–86 (1989).
CAS PubMed Google Scholar
Fick, G. M. & Gabow, P. A. Hereditary and acquired cystic disease of the kidney. Kidney Int 46, 951–964, https://doi.org/10.1038/ki.1994.354 (1994).
Article CAS PubMed Google Scholar
Bae, K. T. et al. Magnetic resonance imaging evaluation of hepatic cysts in early autosomal-dominant polycystic kidney disease: the Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease cohort. Clinical journal of the American Society of Nephrology: CJASN 1, 64–69, https://doi.org/10.2215/cjn.00080605 (2006).
Article PubMed Google Scholar
Alpern, M. B., Dorfman, R. E., Gross, B. H., Gottlieb, C. A. & Sandler, M. A. Seminal vesicle cysts: association with adult polycystic kidney disease. Radiology 180, 79–80, https://doi.org/10.1148/radiology.180.1.2052727 (1991).
Article CAS PubMed Google Scholar
Danaci, M. et al. The prevalence of seminal vesicle cysts in autosomal dominant polycystic kidney disease. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 13, 2825–2828, https://doi.org/10.1093/ndt/13.11.2825 (1998).
Article CAS Google Scholar
Kuo, I. Y., Duong, S. L., Nguyen, L. & Ehrlich, B. E. Decreased Polycystin 2 Levels Result in Non-Renal Cardiac Dysfunction with Aging. PloS one 11, e0153632, https://doi.org/10.1371/journal.pone.0153632 (2016).
Article CAS PubMed PubMed Central Google Scholar
Cai, Y. et al. Identification and Characterization of Polycystin-2, the PKD2 Gene Product. Journal of Biological Chemistry 274, 28557–28565, https://doi.org/10.1074/jbc.274.40.28557 (1999).
Article CAS PubMed Google Scholar
Yoder, B. K., Hou, X. & Guay-Woodford, L. M. The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia. Journal of the American Society of Nephrology 13, 2508, https://doi.org/10.1097/01.ASN.0000029587.47950.25 (2002).
Article CAS PubMed Google Scholar
Kottgen, M. et al. TRPP2 and TRPV4 form a polymodal sensory channel complex. The Journal of cell biology 182, 437–447, https://doi.org/10.1083/jcb.200805124 (2008).
Article CAS PubMed PubMed Central Google Scholar
Walker, R. V. et al. Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model. Nature. Communications 10, 4072, https://doi.org/10.1038/s41467-019-12067-y (2019).
Article Google Scholar
Luo, Y., Vassilev, P. M., Li, X., Kawanabe, Y. & Zhou, J. Native Polycystin 2 Functions as a Plasma Membrane Ca<sup>2 + </sup>-Permeable Cation Channel in Renal Epithelia. Molecular and cellular biology 23, 2600, https://doi.org/10.1128/MCB.23.7.2600-2607.2003 (2003).
Article CAS PubMed PubMed Central Google Scholar
Scheffers, M. S. et al. Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells. Human Molecular Genetics 11, 59–67, https://doi.org/10.1093/hmg/11.1.59 (2002).
Article CAS PubMed Google Scholar
Santoso, N. G., Cebotaru, L. & Guggino, W. B. Polycystin-1, 2, and STIM1 interact with IP(3)R to modulate ER Ca release through the PI3K/Akt pathway. Cellular physiology and biochemistry: international journal of experimental cellular physiology, biochemistry, and pharmacology 27, 715–726, https://doi.org/10.1159/000330080 (2011).
Article CAS Google Scholar
Anyatonwu, G. I., Estrada, M., Tian, X., Somlo, S. & Ehrlich, B. E. Regulation of ryanodine receptor-dependent calcium signaling by polycystin-2. Proceedings of the National Academy of Sciences of the United States of America 104, 6454–6459, https://doi.org/10.1073/pnas.0610324104 (2007).
Article ADS CAS PubMed PubMed Central Google Scholar
Tsiokas, L. et al. Specific association of the gene product of PKD2 with the TRPC1 channel. Proceedings of the National Academy of Sciences of the United States of America 96, 3934–3939, https://doi.org/10.1073/pnas.96.7.3934 (1999).
Article ADS CAS PubMed PubMed Central Google Scholar
Montalbetti, N., Cantero, M. R., Dalghi, M. G. & Cantiello, H. F. Reactive oxygen species inhibit polycystin-2 (TRPP2) cation channel activity in term human syncytiotrophoblast. Placenta 29, 510–518, https://doi.org/10.1016/j.placenta.2008.02.015 (2008).
Article CAS PubMed Google Scholar
Kale, S. et al. Bone marrow stem cells contribute to repair of the ischemically injured renal tubule. The Journal of Clinical Investigation 112, 42–49, https://doi.org/10.1172/JCI17856 (2003).
Article CAS PubMed PubMed Central Google Scholar
Baculis, B. C. et al. Prolonged seizure activity causes caspase dependent cleavage and dysfunction of G-protein activated inwardly rectifying potassium channels. Scientific Reports 7, 12313, https://doi.org/10.1038/s41598-017-12508-y (2017).
Article ADS CAS PubMed PubMed Central Google Scholar
Racine, R. J. Modification of seizure activity by electrical stimulation. II. Motor seizure. Electroencephalography and clinical neurophysiology 32, 281–294 (1972).
Article CAS Google Scholar
Boehringer, R. et al. Chronic Loss of CA2 Transmission Leads to Hippocampal Hyperexcitability. Neuron 94, 642–655.e649, https://doi.org/10.1016/j.neuron.2017.04.014 (2017).
Article CAS PubMed Google Scholar
Cohn, R. et al. A Contraction Stress Model of Hypertrophic Cardiomyopathy due to Sarcomere Mutations. Stem cell reports 12, 71–83, https://doi.org/10.1016/j.stemcr.2018.11.015 (2019).
Article CAS PubMed Google Scholar
Lian, X. et al. Directed cardiomyocyte differentiation from human pluripotent stem cells by modulating Wnt/beta-catenin signaling under fully defined conditions. Nature protocols 8, 162–175, https://doi.org/10.1038/nprot.2012.150 (2013).
Article CAS PubMed Google Scholar
Tohyama, S. et al. Distinct metabolic flow enables large-scale purification of mouse and human pluripotent stem cell-derived cardiomyocytes. Cell stem cell 12, 127–137, https://doi.org/10.1016/j.stem.2012.09.013 (2013).
Article CAS PubMed Google Scholar
Edwards, S. L. et al. A Multiwell Cardiac μGMEA Platform for Action Potential Recordings from Human iPSC-Derived Cardiomyocyte Constructs. Stem cell reports 11, 522–536, https://doi.org/10.1016/j.stemcr.2018.06.016 (2018).
Article PubMed PubMed Central Google Scholar
DesRochers, T. M., Kuo, I. Y., Kimmerling, E. P., Ehrlich, B. E. & Kaplan, D. L. The effects of mycoplasma contamination upon the ability to form bioengineered 3D kidney cysts. PloS one 10, e0120097, https://doi.org/10.1371/journal.pone.0120097 (2015).
Article CAS PubMed PubMed Central Google Scholar
Oslowski, C. M. & Urano, F. In Methods in Enzymology Vol. 490 (ed P. Michael Conn) 71-92 (Academic Press, 2011).
Uchida, K. 4-Hydroxy-2-nonenal: a product and mediator of oxidative stress. Progress in Lipid Research 42, 318–343, https://doi.org/10.1016/S0163-7827(03)00014-6 (2003).
Article CAS PubMed Google Scholar
Brentnall, M., Rodriguez-Menocal, L., De Guevara, R. L., Cepero, E. & Boise, L. H. Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis. BMC Cell Biology 14, 32, https://doi.org/10.1186/1471-2121-14-32 (2013).
Article CAS PubMed PubMed Central Google Scholar

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Acknowledgements

We thank Qi Wang and Dr. Xiaoyong Yang for kindly providing liver cDNA samples from ND- and HFD-fed mice. We thank Dr. Bentley Lim, Eunice Cho (Yale University), and Dr. Olga Buzovetsky (The Rockefeller University) for helpful discussions and edits. We thank Esther Giehl (Charité – Universitätsmedizin Berlin) for the contribution of saline- and ISO-treated murine hearts. Federal and NIH grant support is acknowledged: 5P01DK057751 and P30DK090744 (B.E.E.), F31DK118836 (A.L.B.), 1R01NS083402 and 1R01NS097610 (H.J.C.), T32GM007205 (L.R.S.), and GM007324. We acknowledge the use of the Yale Center for Cellular and Molecular Imaging (NIH grants 5P30DK034989 and OD020142). L.R.S. was supported by a P.D. Soros Fellowship for New Americans. WT and PC2 KO mIMCD-3 cells were created by members of the George M. O’Brien Kidney Center at Yale (P30 DK079310). T.T.F. was supported by a scholarship from the German Academic Scholarship Foundation.

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Parker C. Wilson
Present address: Department of Pathology and Immunology, Washington University in St. Louis, St. Louis, MO, 63110, United States of America

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Department of Cellular and Molecular Physiology, Yale University, New Haven, CT, 06510, United States of America
Allison L. Brill & Barbara E. Ehrlich
Department of Pharmacology, Yale University, New Haven, CT, 06510, United States of America
Tom T. Fischer & Barbara E. Ehrlich
Institute of Pharmacology, Heidelberg University, Heidelberg, Germany
Tom T. Fischer
Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America
Jennifer M. Walters & Hee Jung Chung
Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America
Jennifer M. Walters & Hee Jung Chung
Department of Internal Medicine, Yale University, New Haven, CT, 06510, United States of America
Arnaud Marlier & Lloyd G. Cantley
Department of Biomedical Engineering, Yale University, New Haven, CT, 06510, United States of America
Lorenzo R. Sewanan & Stuart G. Campbell
Department of Pathology, Yale University, New Haven, CT, 06510, United States of America
Parker C. Wilson, Gilbert Moeckel & Marie E. Robert
Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, 63110, United States of America
Eric K. Johnson & Jeanne M. Nerbonne
Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO, 63110, United States of America
Jeanne M. Nerbonne

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Allison L. Brill
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Contributions

A.L.B. and B.E.E. conceived the project. A.L.B., T.T.F., J.F.W., and H.J.C. conducted experiments and analyzed data. A.M., L.R.S., P.C.W., E.K.J., G.M., L.G.C., S.G.C., J.M.N., H.J.C., and M.E.R. contributed reagents. A.L.B. drafted and edited the manuscript. B.E.E. and T.T.F. edited the manuscript. All authors agreed to the final manuscript.

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Correspondence to Barbara E. Ehrlich.

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Brill, A.L., Fischer, T.T., Walters, J.M. et al. Polycystin 2 is increased in disease to protect against stress-induced cell death. Sci Rep 10, 386 (2020). https://doi.org/10.1038/s41598-019-57286-x

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Received: 30 July 2019
Accepted: 23 December 2019
Published: 15 January 2020
DOI: https://doi.org/10.1038/s41598-019-57286-x

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