4.7 Article

Lipid peroxidation regulates podocyte migration and cytoskeletal structure through redox sensitive RhoA signaling

期刊

REDOX BIOLOGY
卷 16, 期 -, 页码 248-254

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.redox.2018.02.024

关键词

Lipid peroxidation; Reactive lipids; Podocyte; RhoA; Cysteine; Chronic kidney disease

资金

  1. NIH DiaComp grant [14GHSU1393, R01-HD085017]
  2. Pennington Foundation
  3. COBRE center grants from the NIH [NIH P20-RR021945]
  4. NORC center grants from the NIH [NIH 1P30-DK072476]

向作者/读者索取更多资源

Early podocyte loss is characteristic of chronic kidney diseases (CKD) in obesity and diabetes. Since treatments for hyperglycemia and hypertension do not prevent podocyte loss, there must be additional factors causing podocyte depletion. The role of oxidative stress has been implicated in CKD but it is not known how exactly free radicals affect podocyte physiology. To assess this relationship, we investigated the effects of lipid radicals on podocytes, as lipid peroxidation is a major form of oxidative stress in diabetes. We found that lipid radicals govern changes in podocyte homeostasis through redox sensitive RhoA signaling: lipid radicals inhibit migration and cause loss of F-actin fibers. These effects were prevented by mutating the redox sensitive cysteines of RhoA. We therefore suggest that in diseases associated with increased lipid peroxidation, lipid radicals can determine podocyte function with potentially pathogenic consequences for kidney physiology.

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