Increased proteinuria causes tubulointerstitial injury due to inflammation in chronic kidney disease (CKD). Iron restriction exhibits protective effects against renal dysfunction; however, its effects against protein overload-induced tubulointerstitial damage remain unclear. Here, we investigated dietary iron restriction effect on tubulointerstitial damage in mice with protein-overload tubulointerstitial injury. Renal tubulointerstitial injury in animal model was induced by intraperitoneal injection of an overdose of bovine serum albumin (BSA). We divided mice into three groups: normal saline + normal diet (ND), BSA + ND, and BSA + iron-restricted diet (IRD). BSA overload induced renal tubulointerstitial injury in the ND mice, which was ameliorated in the IRD mice. Inflammatory cytokines and extracellular matrix mRNA expression was upregulated in BSA + ND mice kidneys and was inhibited by IRD. BSA-induced increase in renal superoxide production, NADPH oxidase activity, and p22phox expression was diminished in the IRD mice. IRD suppression increased BSA-induced renal macrophage infiltration. Moreover, BSA mice exhibited nucleotide-binding oligomerisation domain-like receptor pyrin domain-containing protein (NLRP) inflammasome activation, which was inhibited by IRD. Ferrous iron increased in kidneys with BSA overload and was inhibited by IRD. Thus, iron restriction inhibited oxidative stress and inflammatory changes, contributing to the protective effect against BSA overload-induced tubulointerstitial injury.
The number of patients with chronic kidney disease (CKD) has been increasing worldwide, and the presence of CKD worsens morbidity and mortality. Proteinuria, including albuminuria, is a biomarker for CKD, is associated with renal tubular and tubulointerstitial damage, and causes further progression of kidney injury and deterioration of renal function1, 2. Proteinuria induces tubulointerstitial injury through apoptosis3, inflammation4, epithelial–mesenchymal transition5, and oxidative stress6. Recent studies have demonstrated that nucleotide-binding oligomerisation domain-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome also plays a crucial role in the progression of tubulointerstitial damage induced by protein overload7, 8. Thus, proteinuria is involved in further exacerbation of CKD through various contributing factors.
Iron is an essential trace metal for metabolic processes and enzyme activity in all living organisms. Moreover, iron catalyses the Fenton reaction and consequently causes oxidative stress via hydroxyl radical production9. Therefore, intracellular iron is restrictively controlled by iron transporters, iron-binding proteins, and iron-storage proteins10. Of late, it has been demonstrated that the kidney participates in the regulation of iron metabolism and homeostasis11; therefore, iron is potentially involved in renal pathophysiology. In different experimental animal models, iron is involved in determining the pathological condition of CKD such as diabetic nephropathy12,13,14, hypertensive kidney injury15, 16, and renal fibrosis17, and these diseases are ameliorated by iron reduction in the body. Dietary iron restriction inhibits the increment of urinary albuminuria in db/db mice12; however, it remains unclear whether iron restriction can prevent protein overload-induced renal injury.
In the present study, we determined that dietary iron restriction alleviates protein overload-induced tubulointerstitial injury, and inhibits oxidative stress and inflammatory changes in mice. Moreover, ferrous iron production is elevated in the kidneys with protein overload, suggesting its involvement in the pathological condition of protein-overload renal injury through oxidative stress via the Fenton reaction.
Effects of dietary iron restriction on BSA-induced tubulointerstitial injury
Renal tubulointerstitial injury was induced in mice with BSA overload, and it was alleviated by dietary iron restriction (Fig. 1a (upper) and b). Similar to histological analysis, the mRNA expression of lipocalin-2, a marker of tubulointerstitial damage, was also upregulated in BSA-overload mice, which was inhibited by iron-restricted diet (IRD, Fig. 1c). BSA-induced upregulation of fibrosis-related genes, such as collagen 1 and fibronectin, was also suppressed in mice with IRD (Fig. 1a (middle and lower), and d). These results suggested the favourable effect of dietary iron restriction in protein-overload tubulointerstitial injury.
Dietary iron restriction attenuates the BSA-induced renal inflammatory changes
BSA augmented renal inflammatory cytokines, including TNF-α, MCP-1, IL-6, and PAI-1, which were abolished by iron restriction (Fig. 2a). Increment of macrophage infiltration in the tubulointerstitium and increased F4/80 mRNA expression was observed in mice with BSA overload and was reduced by IRD (Fig. 2b–d).
BSA-induced renal oxidative stress was reduced by iron restriction
BSA promotes oxidative stress production through NADPH oxidase-dependent pathway6. We performed dihydroethidium (DHE) staining to assess oxidative stress production. BSA-induced renal oxidative stress in mice kidneys was reduced by IRD (Fig. 3a and b). The increase in NADPH oxidase activity was elevated in the BSA + ND group mice kidneys and was inhibited by IRD (Fig. 3c). Both mRNA and protein expression of p22phox, a subunit of the NADPH oxidase complex, was augmented in the BSA + ND group mice kidneys and was inhibited in the BSA + IRD group mice (Fig. 3d).
NLRP3 inflammasome activation was abolished by dietary iron restriction
BSA + ND group mice exhibited upregulation of mRNA and protein expression of NLRP3, predominantly in the renal tubule, and this increase was diminished by IRD (Fig. 4a–d). Similarly, the expression of p10 caspase-1, ASC, and mature IL-1β was also upregulated by BSA overload and was inhibited by IRD (Fig. 4c and d).
Changes in iron content and ferrous iron in the kidney
Dietary iron restriction reduced renal iron content and induced mild anaemia in the mice with BSA overload. Although BSA overload did not alter the total iron content in the kidney compared to the vehicle group, renal ferrous iron was increased by BSA overload, and the increase was suppressed by IRD (Table 1 and Fig. 5).
Alteration of renal function and iron-related parameters in the mice with BSA overload
BSA overload resulted in an increase in the blood urea nitrogen (BUN) level, which was ameliorated by IRD. On the other hand, no change in the plasma creatinine level was observed between the three groups. Additionally, no change in the plasma ferritin level was observed between the mice administered with vehicle and the mice with BSA overload. Plasma iron and transferrin saturation (TSAT) were observed to be elevated in the BSA-treated mice. Plasma ferritin, plasma iron and TSAT levels were diminished in the BSA-treated mice with IRD. Plasma hepcidin-1 was also found to be elevated in the mice with BSA overload, which was dramatically reduced by IRD (Table 2).
Proteinuria is an early biomarker for patients with CKD and a causal factor for the progression of CKD by eliciting tubular damage and tubulointerstitial injury. We first demonstrated that BSA overload enhanced ferrous iron levels in the kidney, although the renal total iron content was not altered. Renal iron content is increased in the mice with unilateral ureteral obstruction (UUO) surgery17 or in mice with 5/6 nephrectomy16, indicating that the increment in ferrous iron is due to the increase of total iron content. Furthermore, dietary iron reduction prevented the progression of diabetic nephropathy in the db/db mice, however, no difference was observed in the renal iron content of the control mice and that of the db/db mice12, suggesting the involvement of the labile ferrous iron, rather than the total iron content, in the pathological condition. In cisplatin-induced nephropathy and ischemia-reperfusion injury, bleomycin-detectable iron (iron capable of catalysing the reaction of free radicals is same as ferrous iron) and hydroxyl radical formation increased in the mice kidneys18, 19. It has been clinically observed that urinary catalytic iron increased during diabetic nephropathy or glomerulonephritis20. Thus, ferrous iron increased in these kidney diseases, and may be responsible for their pathological condition. Although the primary mechanism of ferrous iron augmentation remains unclear, labile ferrous iron is potentially involved in different types of kidney injury, and BSA overload-mediated increase in ferrous iron can also be a trigger for causing renal tubulointerstitial injury.
Therefore, protein overload-induced increment in renal ferrous iron suggested the promotion of oxidative stress via the Fenton reaction. As expected, renal superoxide and labile iron levels were reduced by IRD. Similar to this study, it has been observed that renal injuries induced by cisplatin or ischemia–reperfusion were diminished by iron chelation, through the inhibition of hydroxyl radical production, resulting in a decrease in the ferrous iron levels18, 21. In addition to the Fenton reaction, NADPH oxidase activity and p22phox expression was upregulated in the kidneys of mice with protein overload, which was inhibited by dietary iron restriction. Protein overload augments NADPH oxidase activity6. We demonstrated that iron reduction diminished NADPH oxidase activity and p22phox expression in diabetic nephropathy and renal fibrosis induced by unilateral ureteral obstruction12, 17. This supported the findings of our present study, since iron was essential for enzymatic activity of NADPH oxidase22 and biosynthesis of p22phox subunit, which is a haemprotein23. Therefore, protein overload causes oxidative stress through the iron-dependent Fenton reaction and NADPH oxidase in the kidney, and these changes were inhibited by iron reduction, contributing to the alleviation of BSA-induced tubulointerstitial injury.
Consistent with our study, other studies have reported that both pharmacological and dietary iron reduction ameliorated the progression of CKD in various disease models12,13,14, 16, 17. In the present study, BSA-induced tubulointerstitial injury was diminished by iron restriction through the inhibition of oxidative stress, macrophage infiltration, inflammatory cytokines, and fibrosis-related genes. Oxidative stress is well-known to elicit an inflammatory response by activating transcription factors, such as NF-κβ24. Consistent with these findings, iron reduction has been known as an effective approach for reducing macrophage infiltration, inflammatory cytokines, and fibrosis in CKD such as diabetic nephropathy12,13,14, 5/6 nephrectomy16, and UUO-induced renal fibrosis17. This supports the inhibitory effect of iron restriction on renal tubulointerstitial injury induced by BSA overload by suppressing inflammation via reduced oxidative stress production.
The NLRP3 inflammasome plays a crucial role in regulating the caspase-1 activity and cleaving pro-IL-1β into its secreted form25. The NLRP3 inflammasome also contributes in promoting renal inflammation and CKD progression26 and implicates tubulointerstitial injury induced by protein overload7, 8. Similar to the above-mentioned studies, in the present study, BSA overload promoted NLRP3 inflammasome activation in the kidneys, which was suppressed by dietary iron restriction. Regarding the effect of iron on the inflammasome, cellular labile iron acts as a trigger for activating the NLRP3 inflammasome through iron-mediated reactive oxygen species (ROS) production in the macrophage27 and retina28. ROS is an upstream signalling molecule for NLRP3 inflammasome activation29. Collectively, the activation of NLRP3 inflammasome may be caused by ferrous iron-mediated oxidative stress production via the Fenton reaction or NADPH oxidase activation in the kidney. Therefore, iron restriction is also effective in inhibiting BSA-induced augmentation of renal ferrous iron, resulting in the suppression of NLRP3 inflammasome activation by reducing oxidative stress.
Among the biochemical parameters for determining iron status, the levels of plasma hepcidin-1 and TSAT were observed to be elevated in the mice with BSA overload. Hepcidin, a hormone secreted by hepatocytes, is an important regulator for iron metabolism. It acts by downregulating the expression of ferroportin, which is an iron exporter30. Patients with CKD display an elevated level of hepcidin31. Plasma hepcidin concentration, as well as mRNA levels of hepatic hepcidin, is also increased in adenine-induced CKD in mice32. Increased hepcidin level impairs the proper use for intracellular stored iron and the absorption of iron from the duodenum, resulting in the disturbance of systemic iron metabolism in CKD. Therefore, the increase in hepcidin level induced by BSA overload might also be involved in the alteration of iron homeostasis. Although TSAT was higher in BSA-treated mice, there was no difference of stored iron as indicated by plasma ferritin levels and renal iron concentration between vehicle-treated mice and BSA-treated mice, and plasma iron levels were elevated by BSA treatment, which disagree impaired utilization of iron regardless of hepcidin elevation. Further studies are needed to clarify the link between renal dysfunction and systemic iron homeostasis in CKD.
Patients with advanced CKD and end-stage renal dysfunction with renal anaemia are treated with the erythropoiesis-stimulating agent (ESA) along with iron, which is necessary for the effective functioning of ESA33. Further titration studies are necessary to clarify the optimal iron intake and iron status in CKD with respect to kidney function and hematopoiesis. In addition, iron deficiency is also known to stimulate fibroblast growth factor 23 (FGF23), a bone-derived phosphaturic hormone. The level of FGF23 is elevated in patients with CKD. Such elevated FGF23 levels are independently associated with the progression of CKD, cardiovascular events, and mortality34. Therefore, the beneficial effects of IRD on CKD might be offset by an increase in the level of FGF23. Further investigation is required to elucidate the beneficial and adverse effects of iron restriction on CKD.
In conclusion, augmentation of ferrous iron induced by protein overload causes oxidative stress via the Fenton reaction and NADPH oxidase, resulting in renal tubulointerstitial injury and inflammatory changes, which are ameliorated by iron restriction. These observations indicate that iron-mediated oxidative stress results in the pathogenesis of protein overload-induced renal injury.
Materials and Methods
We purchased and used the following commercially available antibodies: anti-interleukin-1β, anti-ASC (apoptosis-associated speck-like protein containing a CARD), anti-caspase-1 (p10), anti-fibronectin (Santa Cruz Biotechnology, Inc., Dallas, TX), anti-NLRP3 (Cell Signalling Technology, Danvers, MA), anti-F4/80 (Bio-Rad Laboratories, Hercules, CA), anti-type I collagen (SouthernBiotech, Birmingham, AL), and anti-β-actin (protein loading control, Cell Signalling Technology).
Animal preparation and procedure
All experimental procedures for mice were performed in accordance with the guidelines of the Animal Research Committee of Tokushima University Graduate School, and the protocol was approved by the Institutional Review Board of Tokushima University Graduate School for animal protection (Permit Number: 14137). The mice were randomly divided into three groups: vehicle with normal diet (ND)-fed group, BSA with ND-fed group, and BSA with IRD-fed group. Seven-week-old male C57BL/6J mice were obtained from Nippon CLEA (Tokyo, Japan) and were maintained with ad libitum access to water and food. Then, mice were either fed with commercially available ND [D03072502 (3.9 mg Fe/100 g food)] or IRD [D03072501 (0.3 mg Fe/100 g food)] (Research Diets, Inc. New Brunswick, NJ). After 1 week, the mice were intraperitoneally injected with BSA. A stepwise increment dose regime of BSA was employed for inducing protein overload tubulointerstitial injury in the mice7. In brief, the initial BSA dose was 2 mg/g body weight on the first day and was increased gradually to the maximum dose of 10 mg/g body weight on day 5, which was maintained for 7 days. For the vehicle-treated group, the mice received intraperitoneal injection of normal saline. On day 12, 24 h after the last BSA dose, the mice were euthanised by intraperitoneally injecting an overdose of pentobarbital, and kidneys were removed and stored at −80 °C until further use.
Preparation of BSA solution
BSA [Cohn fraction V (019–23293); Wako Pure Chemical Industries, Ltd., Osaka, Japan] was dissolved in normal saline, and the final concentration was 330 mg/mL. The concentration of endotoxin in BSA solution was 0.03 ng/mL, as detected by the limulus amebocyte lysate assay (Pierce™ LAL Chromogenic Endotoxin Quantitation Kit, Thermo Fisher Scientific, Inc., Waltham, MA).
Real-time PCR for mRNA quantification
RNA extraction, cDNA synthesis, and quantitative RT-PCR methods have been described previously in detail12. In brief, the tissues were homogenised in the RNAiso reagent (TAKARA Bio, Inc., Otsu, Japan) using a Minilys tissue homogenizer (Bertin Instruments, Montigny-le-Bretonneux, France). RNA extraction and cDNA synthesis were performed according to the manufacturer’s instructions [PrimeScript RT reagent kit with gDNA Eraser (Perfect Real Time); TAKARA Bio, Inc.]. Quantitative RT-PCR was performed using the CFX Connect Real-Time PCR Detection System (BIO-RAD Laboratories Inc., Hercules, CA, USA) with THUNDERBIRD SYBR qPCR Mix (TOYOBO CO., LTD., Osaka, Japan). The primer sets used were as follows: 5′- ACGGCATGGATCTCAAAGAC-3′ and 5′-GTGGGTGAGGAGCACGTAGT-3′ for TNF-α, 5′-GGAGCTCATGATGTGAGCAA-3′ and 5′-GACCAGGCAAGGGAATTACA-3′ for monocyte chemotactic protein-1 (MCP-1), 5′- CCGGAGAGGAGACTTCACAG-3′ and 5′-TCCACGATTTCCCAGAGAAC-3′ for IL-6, 5′-GAGCGGAGAGTACTGGATCG-3′ and 5′-GTTCGGGCTGATGTACCAGT-3′ for collagen-1, 5′-GTCTTTCCGACCAAGAGCAG-3′ and 5′-GACAAAGGCTGTGGAGGAAG-3′ for PAI-1, 5′-ACAGAGCTCAACCTCCCTGA-3′ and 5′-TGTGCTCCTGGTTCTCCT-3′ for fibronectin, 5′-CTGTAACCGGATGGCAAACT-3′ and 5′-CTGTACCCACATGGCTGATG-3′ for F4/80, 5′- GTGGACTCCCATTGAGCCTA-3′ and 5′-CTCCTCTTCACCCTCACTCG-3′ for p22 phox, 5′-TGGAAGAACCAAGGAGCTGT-3′ and 5′-GGTGGGGACAGAGAAGATGA-3′ for lipocalin-2, and 5′-GCTCCAAGCAGATGCAGCA-3′ and 5′-CCGGATGTGAGGCAGCAG-3′ for 36B4 (internal control). The expression levels of all target genes were normalised using 36B4 expression, and the values were compared to the control group in terms of relative fold changes.
Protein extraction and western blot analysis
Protein preparation and western blotting were performed as previously described12. In brief, kidney tissue samples were homogenised with the Minilys bead-based homogeniser (Bertin Instruments, Montigny-le-Bretonneux, France) and proteins were extracted. The extracted proteins were boiled for 5 min in the Laemmli sample buffer and separated using SDS–PAGE. Proteins were transferred onto a polyvinylidene fluoride (PVDF) membrane and the membrane was blocked for 1 h at room temperature. Next, the membrane was incubated individually with each primary antibody overnight at 4 °C, followed by incubation for 1 h with the secondary antibody. Then, immunoreactive bands were detected using a chemiluminescent reagent and visualised by exposure onto an X-ray film or by C-DiGit Blot Scanner (LI–COR, Lincoln, Nebraska, USA). Densitometry of the visualised bands was quantified using the Image J 1.38x software (https://imagej.nih.gov/ij/).
Histological analysis for tubulointerstitial damage
The assessment of renal tubulointerstitial damage has been described previously35. In brief, the kidney tissue samples were fixed in 4% paraformaldehyde and embedded in paraffin. Samples were cut into 3-µm sections, and the sections were stained with haematoxylin and eosin (HE). Tubular injuries were scored in a blinded manner according to the percentage of damage (including atrophy, flattening of the proximal tubule epithelial cells, and tubular dilation) as follows: 0, normal; 1, <20%; 2, 20–40%; 3, 40–60%; 4, 60–80%, and 5, >80%. Ten random microscopic fields per kidney section were used for quantification.
Immunohistochemistry of the kidney samples
Immunohistochemical staining of F4/80 and fibronectin was performed as described previously17. In brief, the paraffin-embedded kidney samples were cut into 3-µm sections, deparaffinised, processed for antigen retrieval using 10 mM citrate buffer at 95 °C for 20 min, and cooled for 20 min. For collagen-1 staining, the frozen tissue sections were used36. Non-fixed kidney tissues were embedded in the Tissue-Tek O.C.T. Compound (Sakura Finetek, Tokyo, Japan) and subjected to snap freezing using the liquid nitrogen–cold isopentane mixture. Samples were cut into 8-µm sections, dried, and fixed in 10% neutral formaldehyde for 10 min. After blocking, the sections were incubated with the primary antibody at 4 °C overnight. Antibody distribution was visualised using a streptavidin–biotin complex assay and a 3,3′-diaminobenzidine (DAB) substrate kit (LSAB + Kit Universal; Dako Japan, Tokyo, Japan). Sections incubated without the primary antibody were used as negative controls. The evaluation of macrophage infiltration in tubulointerstitium was performed as described previously17. Briefly, ten microscopic fields were randomly selected in the renal cortex and the macrophage-positive area was expressed as a percentage of the total area, except the areas under tubular lumen, glomeruli, and vessels, using the ImageJ 1.38x software.
Measurement of tissue iron content
Tissue iron content was measured using an iron assay kit according to the manufacturer’s instructions (Metallo assay; Metallogenics Co., Ltd., Chiba, Japan), as described previously12, 17. In brief, the kidney tissue samples were homogenised in the cell lysis buffer, and the non-centrifuged crude lysates with 0.05 M hydrochloric acid were mixed at regular intervals for 30 min, and centrifuged with 12,000 rpm for 10 min at 4 °C. Subsequently, the supernatants were used for assay. Tissue iron concentration was corrected using tissue weight and expressed as µg/g of wet tissue.
Measurement of NADPH oxidase activity
NADPH oxidase activity was measured as previously described12, 17. In brief, the kidney tissue sample was immediately homogenised in the NADPH oxidase lysis buffer and sonicated for 3 s. The NADPH substrate (final concentration, 300 µM) was added to the renal suspension with lucigenin (5 µM). Luminescence was measured every second for 60 min in a plate reader (SpectraMax Paradigm FilterMaxF3; Molecular Devices Japan, Tokyo, Japan). NADPH activity was expressed as relative luminescence units normalised to the protein concentration.
In situ oxidative stress detection in the kidney tissue
Detection of superoxide production in the kidney was evaluated by DHE staining method as previously described12. Non-fixed frozen tissue sections were washed with PBS, incubated with DHE in PBS (10 µM) in a dark, humidified container at room temperature for 30 min, and observed using fluorescence microscopy.
Detection of renal ferrous iron
RhoNox-1 was used to detect ferrous iron content in the kidney37. The staining method used has been described previously36. First, frozen sections were washed three times in Hank’s balanced salt solution (HBSS) for 5 min, fixed in 10% neutral formaldehyde for 1 min, and washed three times with HBSS for 5 min. Next, the fixed sections were incubated with RhoNox-1 in HBSS (5 µM) in a dark, humidified container at room temperature for 30 min. After washing three times with HBSS, the sections were covered with a small drop of the mounting medium and observed using fluorescence microscopy. The section stained with RhoNox-1 was observed and quantified using fluorescence microscopy.
Haematological and biochemical analysis
Peripheral blood samples were analysed at Shikoku Chuken, K.K. (Kagawa, Japan). The plasma total protein concentration was measured by the bicinchoninic acid assay (BCA) assay. The analysis of plasma albumin, BUN, and TSAT was performed at the Nagahama Life Science Laboratory (Shiga, Japan). The plasma creatinine level was measured using the LabAssay Creatinine kit (Wako Pure Chemical Industries, Ltd., Osaka, Japan). The plasma ferritin concentration was determined using the Mouse Ferritin ELISA kit (Immunology Consultants Laboratory, Newberg, OR) according to the manufacturer’s instructions. The hepcidin-1 concentration in mice was measured using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF–MS38; Medical Care Proteomics Biotechnology Co., Ltd., Kanazawa, Japan).
Data are presented as mean ± standard deviation (SD). Significant differences between the three groups were determined using one-way ANOVA followed by Tukey’s post-hoc test. The differences between data were considered to be statistically significant at P < 0.05.
Burton, C. & Harris, K. P. The role of proteinuria in the progression of chronic renal failure. American journal of kidney diseases: the official journal of the National Kidney Foundation 27, 765–775 (1996).
Eddy, A. A. Proteinuria and interstitial injury. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 19, 277–281 (2004).
Li, X. et al. PKC-delta promotes renal tubular cell apoptosis associated with proteinuria. Journal of the American Society of Nephrology: JASN 21, 1115–1124, doi:10.1681/ASN.2009070760 (2010).
Kuusniemi, A. M. et al. Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change. Kidney international 68, 121–132, doi:10.1111/j.1523-1755.2005.00386.x (2005).
Abbate, M. et al. Proximal tubular cells promote fibrogenesis by TGF-beta1-mediated induction of peritubular myofibroblasts. Kidney international 61, 2066–2077, doi:10.1046/j.1523-1755.2002.00380.x (2002).
Whaley-Connell, A. T. et al. Albumin activation of NAD(P)H oxidase activity is mediated via Rac1 in proximal tubule cells. American journal of nephrology 27, 15–23, doi:10.1159/000098432 (2007).
Zhuang, Y. et al. NLRP3 inflammasome mediates albumin-induced renal tubular injury through impaired mitochondrial function. The Journal of biological chemistry 289, 25101–25111, doi:10.1074/jbc.M114.578260 (2014).
Ding, L. H. et al. Enalapril inhibits tubulointerstitial inflammation and NLRP3 inflammasome expression in BSA-overload nephropathy of rats. Acta pharmacologica Sinica 35, 1293–1301, doi:10.1038/aps.2014.66 (2014).
Kruszewski, M. Labile iron pool: the main determinant of cellular response to oxidative stress. Mutat Res 531, 81–92, doi:S0027510703001623 [pii] (2003).
Cairo, G., Recalcati, S., Pietrangelo, A. & Minotti, G. The iron regulatory proteins: targets and modulators of free radical reactions and oxidative damage. Free Radic Biol Med 32, 1237–1243, doi:S0891584902008250 [pii] (2002).
Martines, A. M. et al. Iron metabolism in the pathogenesis of iron-induced kidney injury. Nature reviews. Nephrology 9, 385–398, doi:10.1038/nrneph.2013.98 (2013).
Ikeda, Y. et al. Dietary iron restriction inhibits progression of diabetic nephropathy in db/db mice. American journal of physiology. Renal physiology 304, F1028–1036, doi:10.1152/ajprenal.00473.2012 (2013).
Morita, T. et al. Chelation of dietary iron prevents iron accumulation and macrophage infiltration in the type I diabetic kidney. European journal of pharmacology 756, 85–91, doi:10.1016/j.ejphar.2015.03.053 (2015).
Matsumoto, M. et al. Iron restriction prevents diabetic nephropathy in Otsuka Long-Evans Tokushima fatty rat. Renal failure 35, 1156–1162, doi:10.3109/0886022X.2013.819729 (2013).
Saito, K. et al. Role of aberrant iron homeostasis in the upregulation of transforming growth factor-beta1 in the kidney of angiotensin II-induced hypertensive rats. Hypertension research: official journal of the Japanese Society of Hypertension 27, 599–607 (2004).
Naito, Y. et al. Effect of iron restriction on renal damage and mineralocorticoid receptor signaling in a rat model of chronic kidney disease. Journal of hypertension 30, 2192–2201, doi:10.1097/HJH.0b013e3283581a64 (2012).
Ikeda, Y. et al. Iron chelation by deferoxamine prevents renal interstitial fibrosis in mice with unilateral ureteral obstruction. PloS one 9, e89355, doi:10.1371/journal.pone.0089355 (2014).
Baliga, R., Zhang, Z., Baliga, M., Ueda, N. & Shah, S. V. In vitro and in vivo evidence suggesting a role for iron in cisplatin-induced nephrotoxicity. Kidney international 53, 394–401, doi:10.1046/j.1523-1755.1998.00767.x (1998).
Baliga, R., Ueda, N. & Shah, S. V. Increase in bleomycin-detectable iron in ischaemia/reperfusion injury to rat kidneys. The Biochemical journal 291(Pt 3), 901–905 (1993).
Shah, S. V., Baliga, R., Rajapurkar, M. & Fonseca, V. A. Oxidants in chronic kidney disease. Journal of the American Society of Nephrology: JASN 18, 16–28, doi:10.1681/ASN.2006050500 (2007).
Paller, M. S. & Hedlund, B. E. Role of iron in postischemic renal injury in the rat. Kidney international 34, 474–480 (1988).
Quinn, M. T. & Gauss, K. A. Structure and regulation of the neutrophil respiratory burst oxidase: comparison with nonphagocyte oxidases. Journal of leukocyte biology 76, 760–781, doi:10.1189/jlb.0404216 (2004).
Yu, L., Zhen, L. & Dinauer, M. C. Biosynthesis of the phagocyte NADPH oxidase cytochrome b558. Role of heme incorporation and heterodimer formation in maturation and stability of gp91phox and p22phox subunits. The Journal of biological chemistry 272, 27288–27294 (1997).
Li, N. & Karin, M. Is NF-kappaB the sensor of oxidative stress? FASEB journal: official publication of the Federation of American Societies for Experimental Biology 13, 1137–1143 (1999).
Ferrero-Miliani, L., Nielsen, O. H., Andersen, P. S. & Girardin, S. E. Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation. Clinical and experimental immunology 147, 227–235, doi:10.1111/j.1365-2249.2006.03261.x (2007).
Vilaysane, A. et al. The NLRP3 inflammasome promotes renal inflammation and contributes to CKD. Journal of the American Society of Nephrology: JASN 21, 1732–1744, doi:10.1681/ASN.2010020143 (2010).
Nakamura, K. et al. Activation of the NLRP3 inflammasome by cellular labile iron. Experimental hematology 44, 116–124, doi:10.1016/j.exphem.2015.11.002 (2016).
Gelfand, B. D. et al. Iron Toxicity in the Retina Requires Alu RNA and the NLRP3 Inflammasome. Cell reports 11, 1686–1693, doi:10.1016/j.celrep.2015.05.023 (2015).
Martinon, F. Signaling by ROS drives inflammasome activation. European journal of immunology 40, 616–619, doi:10.1002/eji.200940168 (2010).
Nemeth, E. et al. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 306, 2090–2093, doi:10.1126/science.1104742 (2004).
Zaritsky, J. et al. Hepcidin–a potential novel biomarker for iron status in chronic kidney disease. Clinical journal of the American Society of Nephrology: CJASN 4, 1051–1056, doi:10.2215/CJN.05931108 (2009).
Hamano, H. et al. The uremic toxin indoxyl sulfate interferes with iron metabolism by regulating hepcidin in chronic kidney disease. Nephrol Dial Transplant. in press (2017).
Tarng, D. C., Huang, T. P., Chen, T. W. & Yang, W. C. Erythropoietin hyporesponsiveness: from iron deficiency to iron overload. Kidney international. Supplement 69, S107–118 (1999).
Wolf, M. Update on fibroblast growth factor 23 in chronic kidney disease. Kidney international 82, 737–747, doi:10.1038/ki.2012.176 (2012).
Jia, Y. et al. Low molecular weight fucoidan protects renal tubular cells from injury induced by albumin overload. Scientific reports 6, 31759, doi:10.1038/srep31759 (2016).
Oshima, K. et al. Iron suppresses erythropoietin expression via oxidative stress-dependent hypoxia-inducible factor-2 alpha inactivation. Laboratory investigation; a journal of technical methods and pathology. doi:10.1038/labinvest.2017.11 (2017).
Hirayama, T., Okuda, T. & Nagasawa, H. A highly selective turn-on fluorescent probe fro iron(II) to visualize labile iron in living cells. Chem Sci 4, 1250–1256, doi:10.1039/c2sc21649c (2013).
Tomosugi, N. et al. Detection of serum hepcidin in renal failure and inflammation by using ProteinChip System. Blood 108, 1381–1387, doi:10.1182/blood-2005-10-4043 (2006).
This work was partly supported by JSPS KAKENHI Grant (No. 15K01716 to Y.I. and 15H02898 to T.T.). The Ichiro Kanehara Foundation provided grant to Y.I. We appreciate the excellent technical advice by the Support Center for Advanced Medical Sciences, Institute of Biomedical Sciences, Tokushima University Graduate School. We would like to thank Editage (www.editage.jp) for help with English language editing.
The authors declare that they have no competing interests.
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Ikeda, Y., Horinouchi, Y., Hamano, H. et al. Dietary iron restriction alleviates renal tubulointerstitial injury induced by protein overload in mice. Sci Rep 7, 10621 (2017). https://doi.org/10.1038/s41598-017-11089-0
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