miR-21 in ischemia/reperfusion injury: a double-edged sword?

Author:

Xu Xialian1,Kriegel Alison J.2,Jiao Xiaoyan1,Liu Hong1,Bai Xiaowen3,Olson Jessica2,Liang Mingyu2,Ding Xiaoqiang1456

Affiliation:

1. Division of Nephrology, Fudan University Zhongshan Hospital, Shanghai, Peoples Republic of China;

2. Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin;

3. Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, Wisconsin;

4. Institutes of Biomedical Sciences of Shanghai Medical School, Fudan University, Shanghai, Peoples Republic of China;

5. Kidney and Dialysis Institute of Shanghai, Shanghai, Peoples Republic of China; and

6. Kidney and Blood Purification Laboratory of Shanghai, Shanghai, Peoples Republic of China

Abstract

MicroRNAs (miRNAs or miRs) are endogenous, small RNA molecules that suppress expression of targeted mRNA. miR-21, one of the most extensively studied miRNAs, is importantly involved in divergent pathophysiological processes relating to ischemia/reperfusion (I/R) injury, such as inflammation and angiogenesis. The role of miR-21 in renal I/R is complex, with both protective and pathological pathways being regulated by miR-21. Preconditioning-induced upregulation of miR-21 contributes to the protection against subsequent renal I/R injury through the targeting of genes such as the proapoptotic gene programmed cell death 4 and interactions between miR-21 and hypoxia-inducible factor. Conversely, long-term elevation of miR-21 may be detrimental to the organ by promoting the development of renal interstitial fibrosis following I/R injury. miR-21 is importantly involved in several pathophysiological processes related to I/R injury including inflammation and angiogenesis as well as the biology of stem cells that could be used to treat I/R injury; however, the effect of miR-21 on these processes in renal I/R injury remains to be studied.

Publisher

American Physiological Society

Subject

Genetics,Physiology

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