Nicotinamide phosphoribosyltransferase (NAMPT) upregulation in human pulmonary artery endothelial cells (hPAECs) is associated with pulmonary arterial hypertension (PAH) progression and pulmonary vascular remodeling. The underlying mechanisms regulating NAMPT expression are still not clear. In this study, we aimed to study the regulation of NAMPT expression by microRNA410 (miR410) in hPAECs and explore the role of miR410 in the pathogenesis of experimental pulmonary hypertension. We show that miR410 targets the 3′ UTR of NAMPT and that, concomitant with NAMPT upregulation, miR410 is downregulated in lungs of mice exposed to hypoxia-induced pulmonary hypertension (HPH). Our results also demonstrate that miR410 directly inhibits NAMPT expression. Overexpression of miR410 in hPAECs inhibits basal and VEGF-induced proliferation, migration and promotes apoptosis of hPAECs, while miR410 inhibition via antagomirs has the opposite effect. Finally, administration of miR410 mimics in vivo attenuated induction of NAMPT in PAECs and prevented the development of HPH in mice. Our results highlight the role of miR410 in the regulation of NAMPT expression in hPAECs and show that miR410 plays a potential role in PAH pathobiology by targeting a modulator of pulmonary vascular remodeling.
Pulmonary arterial hypertension (PAH) is a lethal vasculopathy of complex etiology that involves remodeling of distal pulmonary arteries leading to elevation of pulmonary vascular resistance. This process results in right ventricular (RV) failure and death1. There is still no cure for this disease. Thus, there is an imperative need to explore novel interventional pathways for PAH treatment.
Nicotinamide phosphoribosyl transferase (NAMPT), also named visfatin and pre-B cell colony-enhancing factor (PBEF), is a pleiotropic protein possessing extracellular proinflammatory cytokine-like activity and intracellular enzymatic activity as a phosphoribosyltransferase2,3,4,5,6,7,8. Our previous work demonstrated that NAMPT mediates pulmonary vascular remodeling and that inhibition of NAMPT activity is a potential therapeutic target for pulmonary arterial hypertension9. Specifically, we showed that NAMPT levels in human pulmonary artery endothelial cells (hPAECs) were upregulated in patients with PAH and that NAMPT promoted proliferation of hPAECs and human pulmonary artery smooth muscle cells (hPASMCs) via autocrine and paracrine effects, respectively9. The mechanisms for increased PAEC NAMPT expression in PAH are not known.
As a new class of posttranscriptional regulators of many cardiac and vascular diseases10, microRNAs (miRs) are a group of endogenous, small (approximately 22 nucleotides) non-coding RNAs which regulate gene expression11. Several studies have identified miRs associated with PAH and with experimental models of pulmonary hypertension12,13,14. They may be involved in the control of almost all physiological and pathological cellular processes, including several pathways relevant to pulmonary vascular remodeling. We hypothesized that miRNAs regulate NAMPT expression and could, in turn, affect proliferation, migration and apoptosis of PAECs. These specific miRs may also be therapeutic targets for PAH.
MiR410 targets the UTR of NAMPT in hPAECs
We performed in silico analysis of the human NAMPT 3′UTR to predicted miR response elements. We found 5 potential miRs, including miR-410-3p as the highest predicted target of NAMPT with a high probability of down-regulation (mirSVR score: −1.2151; phastCons score: 0.7995). Figure 1A represents the hsa-miR410-3p putative binding site of miR410 within the 3′-UTR of NAMPT. To determine the interaction of miR410 with the NAMPT 3′-UTR, we overexpressed or inhibited miR410 expression using human miR410 mimics or inhibitors, respectively, in hPAECs co-transfected with a sequence-verified clone of NAMPT-3′UTR reporter vector designed for microRNA target validation. Overexpression of miR410 reduced luciferase activity due to NAMPT-3′UTR binding (Fig. 1B), while transfection of miR410 inhibitors increased the luciferase activity of Wt-luc (Fig. 1C). These effects were not demonstrated in the blank PGL-3 vector and a construct mutated in the predicted miR410-3p binding site.
VEGF downregulates miR410 expression and upregulates NAMPT levels in hPAECs
Vascular endothelial growth factor promotes PAEC proliferation and is a major contributor to PAH pathobiology15. Incubation of hPAECs with VEGF (50 ng/ml) for 24 hours significantly decreased the expression of miR410 (Fig. 2A), and increased NAMPT mRNA and protein levels (Fig. 2B–D).
MiR410 is down-regulated in hypoxia-induced pulmonary hypertension (HPH)
We exposed mice to HPH to investigate the expression of miR410(Fig. 3A) as well as NAMPT mRNA (Fig. 3B) and protein levels (Fig. 3C,D) following 1, 7, 14, and 28 days of 10% O2 exposure. The whole lung expression of miR410 significantly decreased following hypoxia exposure in day 7 (ANOVA: p = 0.05, Tukey post-hoc: p < 0.05), increasing close to baseline levels after days 14 and 28. In contrast an inverse pattern was demonstrated for NAMPT mRNA and protein levels during hypoxia exposure (p = 0.0002, Tukey post-hoc: p < 0.05).
MiR410 regulates the expression of NAMPT in hPAECs
To test if miR410 may be a negative regulator of NAMPT expression, we transfected hPAECs with miR410 mimics (Fig. 4A) and inhibitors (Fig. 4E), respectively. After transfection with miR410 mimics, NAMPT protein and mRNA levels significantly decreased (Fig. 4B–D). While after transfection with miR410 inhibitors, NAMPT mRNA (Fig. 4F) levels did not statistically increase, NAMPT protein levels significantly increased (Fig. 4G,H).
MiR410 regulates the proliferation and migration of hPAECs
To investigate whether modulation of miR410 levels could alter the proliferation and migration of hPAECs, we transfected hPAECs with miR410 mimics or inhibitors in the absence or presence of VEGF stimulation. Results indicated statistically significant differences between the average levels in the four groups (ANOVA, p = 0.026). Overexpression of miR410 mimics reduced the proliferative capacity, and the reduction was significant with 100 nm miR410 treatment (post post-hoc test, p = 0.02) (Fig. 5A), while overexpression of miR410 inhibitors significantly increased hPAECs proliferation at 100 nm (post-hoc test, p = 0.03) (Fig. 5B). Under the same conditions, a similar trend was found for hPAEC migration (Fig. 5C,D).
MiR410 promotes hPAECs apoptosis
Since we have previously shown that NAMPT promotes resistance to apoptosis9, we investigated whether miR410 promotes hPAEC apoptosis. As shown in Fig. 6A,B, miR410 over expression induced hPAEC apoptosis in a dose dependent manner.
In vivo MiR410 overexpression attenuates the progression of HPH
We delivered control non-targeted or miR410 mimics via retro-orbital injection to mice weekly on days 7, 14, 28 and 35 in animals exposed to normoxia or 10% hypoxia. As seen is Supplemental Fig. 1, delivery of micro RNA mimic significantly increased the lung expression of miR410 in both normoxia and hypoxia. In the hypoxia group, mice receiving miR410 mimics were found to have significant attenuation of RVSP elevation and the degree of RVH when compared to controls (Fig. 7A–C). Hypoxia-induced pulmonary vascular remodeling was also attenuated by miR410 mimic treatment (Fig. 7D–F). No significant changes in these parameters occurred in the normoxic group of animals. In the hypoxia group, NAMPT mRNA levels in lung tissues were significantly decreased by administration of miR410 mimic when compared to control. This effect was not seen in the normoxia group (Fig. 7G, Wilcoxon rank sum test, p = 0.35). NAMPT levels in PAECs were significantly decreased in mice receiving miR410 mimics in both normoxic and hypoxic conditions (Fig. 8).
In this study, we investigated the contribution of miR410 to pulmonary vascular remolding in vitro and in vivo. This work expands and complements our previous study9, where we found that NAMPT was upregulated in the plasma, lungs, and PAECs isolated from patients with PAH and in PAECs from different rodent models of PH. Further, we have shown that PAECs from patients with PAH were more proliferative and secrete more NAMPT, which promotes PASMC proliferation in a paracrine fashion9. In this study we identified miR410 as a potential regulator of NAMPT expression. We found that miR-410 is downregulated by VEGF in vitro and by hypoxia in vivo and that these changes are coincident with increased NAMPT expression. In addition, we show that miR-410 inhibits hPAEC proliferation and migration while promoting hPAEC apoptosis and that miR410 overexpression attenuates the development of experimental HPH while reducing the lung overexpression of NAMPT in this model. Thus, our results describe a novel role for miR410 in controlling the proliferation, apoptosis and migration of hPAECs, and affecting pulmonary vascular remodeling via regulation of NAMPT expression.
In PAECs from patients with PAH, cancer-like phenotypes such as uncontrolled vascular cell proliferation, apoptosis resistance, and a shift from oxidative phosphorylation towards glycolysis as an energy source have been well documented16,17. In this context, miR410 may target other genes that may play active roles in the development of PAH. Several studies suggest that miR410 may have cell specific roles in promoting proliferative and pro survival pathways. Mussnich et al. demonstrated that miR410 is downregulated in gonadotroph tumors and targets Cyclin B1 (CCNB1) at protein and mRNA levels, decreasing cell proliferation18. Similar findings demonstrating a tumor suppressor role for miR410 were also shown in lung cancer, osteosarcoma, colorectal cancer, breast cancer, cholangiocarcinoma, glioma, oral squamous cell carcinoma and pancreatic cancer19,20,21,22,23,24,25. On the other hand, Li et al. have showed that miR410 targets bromodomain-containing protein 7 (BRD7) and promotes progression of non-small cell lung cancer (NSCLC) via modulation of cell proliferation, migration, and invasion due to downregulation of BRD7 leading to an increase of Akt phosphorylation26. Studies have also described oncogenic properties of miR410 in the context of other malignancies27,28,29. Finally, miR410 has been shown to downregulate IL-10 expression in T cells via suppression of the transcriptional activity of STAT30, a transcriptional factor known to be involved in PAH pathobiology31.
The exact mechanistic role of VEGF and VEGF-dependent signaling in PAH is not completely understood but abnormalities in this pathway have been are well documented in human and experimental pulmonary hypertension32,33. Our data suggest that VEGF downregulates miR410 expression which in turn influences NAMPT expression and PAEC proliferation, migration and apoptosis. Interestingly, miR410 suppresses VEGF expression through interaction with the 3′UTR of the VEGF messenger RNA and overexpression of a miR-410 mimic effectively suppresses VEGF expression in vitro and prevents retinal angiogenesis in a model of retinal neovascularization34. Similar findings were also reported in osteosarcoma cell lines where the expression of VEGF and miR-410 where inversely correlated and miR-410 overexpression resulted in decreased osteosarcoma cell proliferation and migration and increased apoptosis20. Taken together, these data suggest the presence of a feedback loop regulating the expression of these two mediators. Further studies are needed to test whether these interactions involve NAMPT directly or indirectly.
MiR-410 may also potentially affect right ventricular remodeling and dysfunction associated with PAH. Clark and Naya have shown that overexpression of miR-410 promotes cardiomyocyte proliferation by targeting Cited2; a transcriptional coactivator that has been linked to important developmental processes in the heart35. In a follow up study, the same group demonstrated that together with miR-495, miR-410 expression was increased in animal models of myocardial infarction, left ventricular hypertrophy and dystrophic cardiomyopathies; and that silencing of miR-410 and/or miR-495 blunted cardiomyocyte hypertrophy in vitro36.
Micro-RNAs are candidate therapeutic targets and biomarkers for PAH (as reviewed by Pullamsetti et al.37 and Huston et al.38). For instance, in one of our previous studies14, miR1 has been identified as an important regulator of SphK1 expression in PASMCs and a potential therapeutic target for the treatment of PH. Our in silico analyses, however, do not suggest that miR1 or other recently reported PAH-related micro RNAs are predicted to regulate NAMPT expression. As previously discussed, miR-410 regulates VEGF expression and similar interactions with other genes and micro RNAs involved in PAH are also possible.
Our results suggest that miR-410 has a role in regulating pulmonary vascular remodeling. There are, however, several limitations in the current study. First, validation of miR410 is lacking in samples from patients with PAH. Second, in this study only a mouse model of hypoxia mediated PH model was used. This model induces a mild PH phenotype, and we have not tested the effect of overexpressing miR410 in rodent models of severe PH. Evaluation of miR410 expression levels in PAH patients’ blood, lung tissues and PAECs and the effect of overexpressing miR410 in rodent models of severe PH warrant further investigations.
In summary, we show that miR410 plays a potential role in PH pathobiology by targeting NAMPT, a modulator of pulmonary vascular remodeling. Overexpression of miR410 in the pulmonary circulation may have a therapeutic effect in PAH.
Materials and Methods
Bioinformatics analysis and miRNA prediction
In silico analysis for microRNA target prediction was completed via the MicroRNA.org target prediction resource, utilizing miRSVR < −1.10 and PhastCons scores >0.70. and with further 3′- UTR sequence target sites prediction using miRDB.org as we have previously described14.
Human cell lines
A primary Human pulmonary artery endothelial cell (hPAEC) line from Lonza (CC-2530) was used in this study. Vascular endothelial growth factor (VEGF, 293-VE, R&D System) was used at a final concentration of 50 ng/ml. MiR410 mimics, inhibitors and controls (50–100 nM, Qiagen) were transfected to hPAECs using lipofectamine (Thermo Fisher Scientific) per manufacturer’s instructions.
Transient transfections and reporter assays
Mir VanaTM miRNA-410-3P mimics or inhibitors and their corresponding negative controls were used for all microRNA transfection studies (Thermo Fisher Scientific). To construct the luciferase- NAMPT 3′-UTR (Wt-luc) reporter plasmid, a 227 bp 3′-UTR of human NAMPT gene containing the predicted miR410-3p binding site was amplified from human genomic DNA and inserted into downstream of the luciferase reporter gene in the pGL3-Promoter vector (Promega) through the XbaI endonuclease restriction site. We mutated the predicted miR410-3p binding site on the Wt-luc reporter plasmid to generate the Mut-luc reporter using the QuikChange Lightning Site-Directed Mutagenesis Kit (Stratagene, La Jolla, CA). All constructs were sequenced for confirmation.
hPAECs were plated in 12-well plates, and co-transfected with 1 μg of either Wt-luc or Mut-luc reporter plasmid, 50 ng of Renilla reporter plasmid and 50 pmole control or miR410-3p mimics/inhibitors using Lipofectamine 2000 reagent (Invitrogen). The cells were lysed twenty-four hours after transfection, and the luciferase activity was measured using Dual-Luciferase Reporter Assay System (Promega) on GloMax®-96 Microplate luminometer (Promega). Relative luciferase activities were calculated by comparing the firefly/renilla luciferase ratio.
Western blot analysis
As we have previously described9,14,39, lung tissues were perfused with PBS to remove blood and homogenized using RIPA buffer (Sigma) supplemented with protease and phosphatase inhibitor cocktails (Calbiochem). Cells were washed with PBS and protein was extracted using the same modified RIPA buffer solution. Proteins (10–25 μg) were separated on Mini-Protean TGX precast gels (Bio-Rad), transferred to nitrocellulose membranes, and blocked in 5% nonfat milk. Membranes were then probed with primary and secondary antibodies and bands visualized by ECL (Pierce) per manufacturer’s instructions. Densitometry was used to quantify protein levels using ImageJ software, and expression levels were normalized to β-actin. The primary antibodies used were NAMPT, and HRP-conjugated β-actin (Cell Signaling Technology). An anti-rabbit IgG HRP-linked secondary antibody was used (Cell Signaling Technology).
Cell proliferation was determined using a 5-bromo-2’-deoxyuridine (BrdU) incorporation assay (QIA58; Calbiochem) per manufacturer’s instructions, as we have previously described,9,14,39. Starting cell densities of hPAEC 5,000 cells/well were used in a 96-well format.
Cell migration assays
Cell migration was determined using a quantitative transwell assay as previously described9. In brief, 1 × 105 cells were added into a transwell insert with 8-μm pores in 1 ml of basal medium. Cells were then incubated with miR410 mimic/mimic control or inhibitor/inhibitor control for 24 hr prior to transferring to the transwell insert. Cells were fixed and stained using 0.5% crystal violet staining solution, and imaged. Five random fields were imaged per sample to obtain a total cell count. Migrated cells were scraped away from the top of the filter and the migrated bottom layer of cells were imaged and quantified. Relative rate of cell migration was calculated as the migrated cell numbers on the filter normalized by the control group.
In Situ BrdU- Red TUNEL assay
We performed TdT-UTP nick end labeling (TUNEL) method to label 3′-end of fragmented DNA of the apoptotic PASMCs. Three groups of cells cultured in 6-well plates were treated as described in the mitochondrial depolarization assay, then fixed with 4% paraform phosphate buffer saline, rinsed with PBS, then used in situ BrdU-Red DNA fragmentation (TUNEL) cell apoptosis detection kit (Abcam®, Cambridge, MA). The percentage of positive cells to whole PAECs, identified as apoptosis indices (AI), was calculated.
MiRNA PCR analysis and quantitative real-time reverse transcription PCR (qRT-PCR)
Total RNA containing miRNA was isolated from hPASMC and lung tissue samples using QIAzol lysis reagent and column purified using a miRNeasy kit (Qiagen). After quantification with Nanodrop 2000 spectrophotometer (ThermoScientific, Rockford, IL), miRNAs were reversely transcribed using a RT2 miRNA First Strand Kit (SABiosciences, Frederick, MD). For qRT-PCR analysis of miRNA expression, a poly (A) tail was first added to the 3′-end of miRNAs using a Poly (A) Polymerase Tailing Kit (Epicentre Biotechnologies, Madison, WI). Poly (A) tailed-miRNAs were then reversely transcribed using M-MLV Reverse Transcriptase (Invitrogen, Grand Island, NY) with a poly (T) adaptor, which includes a poly (T) sequence and a sequence complementary to the universal primer used in following qRT-PCR analysis. SNORD44, SNORD47 and SNORD48 were used as internal controls. The expression of mRNAs was determined using specific TaqMan primer assays (Applied Biosystems) with GAPDH used as an internal control. Real-time PCR analysis was performed using a CFX384 system (Bio-Rad), and relative changes in mRNA and miRNA expression were calculated after normalization to their respective internal controls using the comparative Ct method.
Animal model of hypoxia induced pulmonary hypertension
All animal procedures were reviewed and approved by the University of Illinois at Chicago Animal Care and Use Committee. All experiments were performed in accordance with relevant guidelines and regulations.
In the mouse model of hypoxia-mediated pulmonary hypertension (HPH), 8-wk old male C57BL/6 mice were exposed to normoxia or hypoxia (10% O2) for 1d-4wks (n = 3–5/group). HPH development was assessed by measuring right ventricular systolic pressure (RVSP) via a pressure transducer catheter (Millar) as a surrogate of pulmonary artery pressure, right ventricular hypertrophy as a weight ratio of the right ventricle divided by the sum of left ventricle and septum (RV/LV + S)9,14,39. Paraffinized lung tissue sections were stained with hematoxylin and eosin. Vessel thickness was measured using Aperio ImageScope software, approximately 20 muscular arteries with diameters 50–100 μm or less than 50 μm per lung section. Pulmonary vascular remodeling was calculated as ([external vessel area – internal vessel area]/external vessel area), as previously described39.
In reversal studies, mice were exposed to normoxia or hypoxia for five weeks (n = 6/group). Animal-grade mirVana miRNA mimics or negative miRNA control (Thermo Fisher Scientific) were prepared with Invivofectamine 3.0 reagent (Thermo Fisher Scientific) per manufacturer’s instructions and injected to mice retro-orbitally (6.8 mg/kg body weight) after one-week normoxia or hypoxia (10% O2) exposure, and then continued for another four weeks. Injections were repeated once per week during the experimental period. One day after the final injection, we assessed HPH development by measuring RVSP, RVH, and pulmonary arterial remodeling as described above. Lung, heart, and blood were isolated for further analysis.
Lung tissue immunofluorescence staining
Paraffin-embedded lung tissue sections were deparaffinized with xylene and rehydrated. Antigen retrieval was employed before blocking in PBS with 10% normal goat serum, 0.1% BSA, 0.3% TX-100. The antigen retrieval solution is Tris-EDTA buffer (10 mM Tris Base, 1 mM EDTA solution, 0.05% Tween 20, pH 9.0). The dilutions for rabbit against NAMPT (Bethyl Laboratories, Inc. catalog# A300-372A) and mouse against von Willebrand factor (VWF, catalog# MA5-14029, Invitrogen) are 1:100. Secondary antibodies for NAMPT and VWF were Alexa Fluor® 593 Donkey anti-Rabbit IgG antibody (1:500) and Alexa Fluor® 593 goat anti-mouse IgG antibody (1:500), respectively. An anti-fade mounting media with DAPI (Life Science Inc) was used to fix the coverslip to a slide. The slides were examined using a a ZEISS Z1 AxioObserver fluorescence microscope (Carl Zeiss, Oberkochen, Germany).
Results are shown as mean ± SEM. Experiments repeated at least three times and Graphpad Prism 4.0 software was used for statistical analysis. Normality of the data was assessed with Bartlett’s test. ANOVAs and Kruskal-Wallis tests were used for normal and non-normal data respectively. Tukey, Sidak and Dunn’s post hoc tests were used for pair-wise comparison. Samples were excluded if they failed Grubbs’ outlier test. p < 0.05 was considered statistically significant.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Boucherat, O., Potus, F. & Bonnet, S. microRNA and Pulmonary Hypertension. Adv Exp Med Biol 888, 237–252, https://doi.org/10.1007/978-3-319-22671-2_12 (2015).
Revollo, J. R., Grimm, A. A. & Imai, S. The regulation of nicotinamide adenine dinucleotide biosynthesis by Nampt/PBEF/visfatin in mammals. Curr Opin Gastroenterol 23, 164–170, https://doi.org/10.1097/MOG.0b013e32801b3c8f (2007).
Sommer, G. et al. Visfatin/PBEF/Nampt: structure, regulation and potential function of a novel adipokine. Clin Sci (Lond) 115, 13–23, https://doi.org/10.1042/CS20070226 (2008).
Imai, S. Nicotinamide phosphoribosyltransferase (Nampt): a link between NAD biology, metabolism, and diseases. Curr Pharm Des 15, 20–28 (2009).
Galli, M., Van Gool, F., Rongvaux, A., Andris, F. & Leo, O. The nicotinamide phosphoribosyltransferase: a molecular link between metabolism, inflammation, and cancer. Cancer Res 70, 8–11, https://doi.org/10.1158/0008-5472.CAN-09-2465 (2010).
Dahl, T. B., Holm, S., Aukrust, P. & Halvorsen, B. Visfatin/NAMPT: a multifaceted molecule with diverse roles in physiology and pathophysiology. Annu Rev Nutr 32, 229–243, https://doi.org/10.1146/annurev-nutr-071811-150746 (2012).
Sun, Z., Lei, H. & Zhang, Z. Pre-B cell colony enhancing factor (PBEF), a cytokine with multiple physiological functions. Cytokine Growth Factor Rev 24, 433–442, https://doi.org/10.1016/j.cytogfr.2013.05.006 (2013).
Garten, A. et al. Physiological and pathophysiological roles of NAMPT and NAD metabolism. Nat Rev Endocrinol 11, 535–546, https://doi.org/10.1038/nrendo.2015.117 (2015).
Chen, J. et al. Nicotinamide Phosphoribosyltransferase Promotes Pulmonary Vascular Remodeling and Is a Therapeutic Target in Pulmonary Arterial Hypertension. Circulation 135, 1532–1546, https://doi.org/10.1161/CIRCULATIONAHA.116.024557 (2017).
Gupta, S. & Li, L. Modulation of miRNAs in Pulmonary Hypertension. Int J Hypertens 2015, 169069, https://doi.org/10.1155/2015/169069 (2015).
Li, T., Pan, H. & Li, R. The dual regulatory role of miR-204 in cancer. Tumour biology: the journal of the International Society for Oncodevelopmental Biology and Medicine 37, 11667–11677, https://doi.org/10.1007/s13277-016-5144-5 (2016).
Liu, H. et al. Upregulation of MicroRNA-214 Contributes to the Development of Vascular Remodeling in Hypoxia-induced Pulmonary Hypertension Via Targeting CCNL2. Scientific reports 6, 24661, https://doi.org/10.1038/srep24661 (2016).
Kang, B. Y. et al. Peroxisome Proliferator-Activated Receptor gamma and microRNA 98 in Hypoxia-Induced Endothelin-1 Signaling. American journal of respiratory cell and molecular biology 54, 136–146, https://doi.org/10.1165/rcmb.2014-0337OC (2016).
Sysol, J. R. et al. Micro-RNA-1 is decreased by hypoxia and contributes to the development of pulmonary vascular remodeling via regulation of sphingosine kinase 1. Am J Physiol Lung Cell Mol Physiol 314, L461–L472, https://doi.org/10.1152/ajplung.00057.2017 (2018).
Masri, F. A. et al. Hyperproliferative apoptosis-resistant endothelial cells in idiopathic pulmonary arterial hypertension. Am J Physiol Lung Cell Mol Physiol 293, L548–554, https://doi.org/10.1152/ajplung.00428.2006 (2007).
Guignabert, C. et al. Pathogenesis of pulmonary arterial hypertension: lessons from cancer. Eur Respir Rev 22, 543–551, https://doi.org/10.1183/09059180.00007513 (2013).
Rai, P. R. et al. The cancer paradigm of severe pulmonary arterial hypertension. Am J Respir Crit Care Med 178, 558–564, https://doi.org/10.1164/rccm.200709-1369PP (2008).
Mussnich, P. et al. Downregulation of miR-410 targeting the cyclin B1 gene plays a role in pituitary gonadotroph tumors. Cell Cycle 14, 2590–2597, https://doi.org/10.1080/15384101.2015.1064207 (2015).
Zhao, D., Jia, P., Wang, W. & Zhang, G. VEGF-mediated suppression of cell proliferation and invasion by miR-410 in osteosarcoma. Mol Cell Biochem 400, 87–95, https://doi.org/10.1007/s11010-014-2265-2 (2015).
Liu, C., Zhang, A., Cheng, L. & Gao, Y. miR410 regulates apoptosis by targeting Bak1 in human colorectal cancer cells. Molecular medicine reports 14, 467–473, https://doi.org/10.3892/mmr.2016.5271 (2016).
Zhang, Y. F. et al. miR-410-3p suppresses breast cancer progression by targeting Snail. Oncology reports 36, 480–486, https://doi.org/10.3892/or.2016.4828 (2016).
Palumbo, T. et al. A functional microRNA library screen reveals miR-410 as a novel anti-apoptotic regulator of cholangiocarcinoma. BMC cancer 16, 353, https://doi.org/10.1186/s12885-016-2384-0 (2016).
Wang, Z. H. et al. Long non-coding RNA CCAT1 promotes glioma cell proliferation via inhibiting microRNA-410. Biochemical and biophysical research communications 480, 715–720, https://doi.org/10.1016/j.bbrc.2016.10.047 (2016).
Shiah, S. G. et al. Downregulated miR329 and miR410 promote the proliferation and invasion of oral squamous cell carcinoma by targeting Wnt-7b. Cancer research 74, 7560–7572, https://doi.org/10.1158/0008-5472.can-14-0978 (2014).
Guo, R., Gu, J., Zhang, Z., Wang, Y. & Gu, C. MicroRNA-410 functions as a tumor suppressor by targeting angiotensin II type 1 receptor in pancreatic cancer. IUBMB life 67, 42–53, https://doi.org/10.1002/iub.1342 (2015).
Li, D. et al. MicroRNA-410 promotes cell proliferation by targeting BRD7 in non-small cell lung cancer. FEBS Lett 589, 2218–2223, https://doi.org/10.1016/j.febslet.2015.06.031 (2015).
Zhang, X. et al. MicroRNA-410 acts as oncogene in NSCLC through downregulating SLC34A2 via activating Wnt/beta-catenin pathway. Oncotarget 7, 14569–14585, https://doi.org/10.18632/oncotarget.7538 (2016).
Wang, Y. et al. MiR-410 is overexpressed in liver and colorectal tumors and enhances tumor cell growth by silencing FHL1 via a direct/indirect mechanism. PLoS One 9, e108708, https://doi.org/10.1371/journal.pone.0108708 (2014).
Ke, X. et al. MiR-410 induces stemness by inhibiting Gsk3beta but upregulating beta-catenin in non-small cells lung cancer. Oncotarget 8, 11356–11371, https://doi.org/10.18632/oncotarget.14529 (2017).
Liu, D. et al. MiR-410 Down-Regulates the Expression of Interleukin-10 by Targeting STAT3 in the Pathogenesis of Systemic Lupus Erythematosus. Cell Physiol Biochem 39, 303–315, https://doi.org/10.1159/000445625 (2016).
Paulin, R., Meloche, J. & Bonnet, S. STAT3 signaling in pulmonary arterial hypertension. JAKSTAT 1, 223–233, https://doi.org/10.4161/jkst.22366 (2012).
Voelkel, N. F. & Gomez-Arroyo, J. The role of vascular endothelial growth factor in pulmonary arterial hypertension. The angiogenesis paradox. American journal of respiratory cell and molecular biology 51, 474–484, https://doi.org/10.1165/rcmb.2014-0045TR (2014).
Sutendra, G. & Michelakis, E. D. Pulmonary arterial hypertension: challenges in translational research and a vision for change. Science translational medicine 5, 208sr205, https://doi.org/10.1126/scitranslmed.3005428 (2013).
Chen, N. et al. MicroRNA-410 reduces the expression of vascular endothelial growth factor and inhibits oxygen-induced retinal neovascularization. PLoS One 9, e95665, https://doi.org/10.1371/journal.pone.0095665 (2014).
Clark, A. L. & Naya, F. J. MicroRNAs in the Myocyte Enhancer Factor 2 (MEF2)-regulated Gtl2-Dio3 Noncoding RNA Locus Promote Cardiomyocyte Proliferation by Targeting the Transcriptional Coactivator Cited2. J Biol Chem 290, 23162–23172, https://doi.org/10.1074/jbc.M115.672659 (2015).
Clark, A. L. et al. miR-410 and miR-495 Are Dynamically Regulated in Diverse Cardiomyopathies and Their Inhibition Attenuates Pathological Hypertrophy. PLoS One 11, e0151515, https://doi.org/10.1371/journal.pone.0151515 (2016).
Pullamsetti, S. S., Perros, F., Chelladurai, P., Yuan, J. & Stenmark, K. Transcription factors, transcriptional coregulators, and epigenetic modulation in the control of pulmonary vascular cell phenotype: therapeutic implications for pulmonary hypertension (2015 Grover Conference series). Pulm Circ 6, 448–464, doi:10.1086/688908 (2016).
Huston, J. H. & Ryan, J. J. The emerging role of epigenetics in pulmonary arterial hypertension: an important avenue for clinical trials (2015 Grover Conference Series). Pulm Circ 6, 274–284, doi:10.1086/687765 (2016).
Chen, J. et al. The sphingosine kinase 1/sphingosine-1-phosphate pathway in pulmonary arterial hypertension. Am J Respir Crit Care Med 190, 1032–1043, https://doi.org/10.1164/rccm.201401-0121OC (2014).
The authors thank Drs Guofei Zhou, Chaoxiong Zhang, Xinyan Qu, Shaoxia Lin, Nicole Jones for technical support. This work was supported grants from the National Heart, Lung, and Blood Institute of the National Institutes of Health R01 HL111656, R01 HL127342, and R01 HL133951 to RFM.
The authors declare no competing interests.
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Gao, H., Chen, J., Chen, T. et al. MicroRNA410 Inhibits Pulmonary Vascular Remodeling via Regulation of Nicotinamide Phosphoribosyltransferase. Sci Rep 9, 9949 (2019). https://doi.org/10.1038/s41598-019-46352-z
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