Ferrostatin-1 alleviates oxalate-induced renal tubular epithelial cell injury, fibrosis and calcium oxalate stone formation by inhibiting ferroptosis

被引:45
作者
Xie, Jinna [1 ]
Ye, Zehua [1 ]
Li, Lei [1 ]
Xia, Yuqi [1 ]
Yuan, Run [1 ]
Ruan, Yuan [1 ]
Zhou, Xiangjun [1 ,2 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Urol, Wuhan 430060, Hubei, Peoples R China
[2] Wuhan Univ, Renmin Hosp, Dept Urol, 238 Jiefang Rd, Wuhan 430060, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
calcium oxalate stone; ferroptosis; ferrostatin-1; renal tubular epithelial cell; chronic kidney disease; ACUTE KIDNEY INJURY; DISEASE;
D O I
10.3892/mmr.2022.12772
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study aimed to evaluate the role and mechanism of ferrostatin-1 (Fer-1) in oxalate (Ox)-induced renal tubular epithelial cell injury, fibrosis, and calcium oxalate (CaOx) stone formation. A CaOx model in mice kidneys was established via intraperitoneal injection of 80 mg/kg glyoxylic acid for 14 days. The mice were randomly divided into three groups (n=6), namely, the control (Con), the CaOx group, and the CaOx + Fer-1 group. Cultured human renal tubular epithelial cells (HK-2 cells) were randomly divided into three groups (n=3), namely, the control (Con), the Ox group, and the Ox + Fer-1 group. The levels of heme oxygenase 1 (HO-1), superoxide dismutase 2 (SOD2), glutathione peroxidase 4 (GPX4), and solute carrier family 7 member 11 (SLC7A11) were assessed by immunofluorescence and western blot analysis. Renal tubular injury and apoptosis were evaluated by H&E and TUNEL staining. Kidney interstitial fibrosis was evaluated by Masson and Sirius red staining, and the levels of E-cadherin, vimentin and alpha-SMA were detected by immunofluorescence or western blot analysis. Mitochondrial structure was observed using a transmission electron microscope. The levels of reactive oxygen species (ROS) were determined by flow cytometry and CaOx stone formation was evaluated by von Kossa staining. The results revealed that in comparison with the Con group, mitochondrial injury under glyoxylic acid treatment was observed by TEM. The expression of GPX4 and SLC7A11 in the CaOx and Ox groups was downregulated (P<0.05), whereas the expression of HO-1 and SOD2 was upregulated (P<0.05). Renal tissue damage, apoptosis of renal tubular epithelial cells, and interstitial fibrosis were increased in the CaOx and Ox groups (P<0.05). In comparison with the CaOx or Ox group, the expression of GPX4 and SLC7A11 in the CaOx + Fer-1 or Ox + Fer-1 group was upregulated (P<0.05), whereas that of HO-1 and SOD2 was downregulated (P<0.05). Renal tissue damage, apoptosis of renal tubular epithelial cells and interstitial fibrosis were decreased following Fer-1 treatment (P<0.05). The ROS level was also decreased following Fer-1 treatment. Moreover, CaOx stone formation was decreased in the CaOx + Fer-1 group (P<0.05). In conclusion, Fer-1 alleviated Ox-induced renal tubular epithelial cell injury, fibrosis, and CaOx stone formation by inhibiting ferroptosis.
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页数:12
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共 38 条
[1]   NFS1 undergoes positive selection in lung tumours and protects cells from ferroptosis [J].
Alvarez, Samantha W. ;
Sviderskiy, Vladislav O. ;
Terzi, Erdem M. ;
Papagiannakopoulos, Thales ;
Moreira, Andre L. ;
Adams, Sylvia ;
Sabatini, David M. ;
Birsoy, Kivanc ;
Possemato, Richard .
NATURE, 2017, 551 (7682) :639-+
[2]   Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice [J].
Angeli, Jose Pedro Friedmann ;
Schneider, Manuela ;
Proneth, Bettina ;
Tyurina, Yulia Y. ;
Tyurin, Vladimir A. ;
Hammond, Victoria J. ;
Herbach, Nadja ;
Aichler, Michaela ;
Walch, Axel ;
Eggenhofer, Elke ;
Basavarajappa, Devaraj ;
Radmark, Olof ;
Kobayashi, Sho ;
Seibt, Tobias ;
Beck, Heike ;
Neff, Frauke ;
Esposito, Irene ;
Wanke, Ruediger ;
Foerster, Heidi ;
Yefremova, Olena ;
Heinrichmeyer, Marc ;
Bornkamm, Georg W. ;
Geissler, Edward K. ;
Thomas, Stephen B. ;
Stockwell, Brent R. ;
O'Donnell, Valerie B. ;
Kagan, Valerian E. ;
Schick, Joel A. ;
Conrad, Marcus .
NATURE CELL BIOLOGY, 2014, 16 (12) :1180-U120
[3]   Renal Inflammation and Fibrosis: A Double-edged Sword [J].
Black, Laurence M. ;
Lever, Jeremie M. ;
Agarwal, Anupam .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2019, 67 (09) :663-681
[4]   Etiologies, Clinical Features, and Outcome of Oxalate Nephropathy [J].
Buysschaert, Benoit ;
Aydin, Selda ;
Morelle, Johann ;
Gillion, Valentine ;
Jadoul, Michel ;
Demoulin, Nathalie .
KIDNEY INTERNATIONAL REPORTS, 2020, 5 (09) :1503-1509
[5]   Acute kidney injury and chronic kidney disease: an integrated clinical syndrome [J].
Chawla, Lakhmir S. ;
Kimmel, Paul L. .
KIDNEY INTERNATIONAL, 2012, 82 (05) :516-524
[6]   Revisiting the intersection of amyloid, pathologically modified tau and iron in Alzheimer's disease from a ferroptosis perspective [J].
Derry, Paul J. ;
Hegde, Muralidhar L. ;
Jackson, George R. ;
Kayed, Rakez ;
Tour, James M. ;
Tsai, Ah-Lim ;
Kent, Thomas A. .
PROGRESS IN NEUROBIOLOGY, 2020, 184
[7]   Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death [J].
Dixon, Scott J. ;
Lemberg, Kathryn M. ;
Lamprecht, Michael R. ;
Skouta, Rachid ;
Zaitsev, Eleina M. ;
Gleason, Caroline E. ;
Patel, Darpan N. ;
Bauer, Andras J. ;
Cantley, Alexandra M. ;
Yang, Wan Seok ;
Morrison, Barclay, III ;
Stockwell, Brent R. .
CELL, 2012, 149 (05) :1060-1072
[8]   Lipid Peroxidation and GPX4 Inhibition Are Common Causes for Myofibroblast Differentiation and Ferroptosis [J].
Gong, Yue ;
Wang, Nan ;
Liu, Naiguo ;
Dong, Hongliang .
DNA AND CELL BIOLOGY, 2019, 38 (07) :725-733
[9]   VDR activation attenuate cisplatin induced AKI by inhibiting ferroptosis [J].
Hu, Zhaoxin ;
Zhang, Hao ;
Yi, Bin ;
Yang, Shikun ;
Liu, Jun ;
Hu, Jing ;
Wang, Jianwen ;
Cao, Ke ;
Zhang, Wei .
CELL DEATH & DISEASE, 2020, 11 (01)
[10]   Emerging Role of Ferroptosis in Acute Kidney Injury [J].
Hu, Zhaoxin ;
Zhang, Hao ;
Yang, Shi-kun ;
Wu, Xueqin ;
He, Dong ;
Cao, Ke ;
Zhang, Wei .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2019, 2019