SENP1 reduces oxidative stress and apoptosis in renal ischaemia–reperfusion injury by deSUMOylation of HIF‐1α

Abstract

AbstractRenal ischaemia–reperfusion injury (RIRI) is a primary cause of acute kidney damage, occurring frequently in situations like renal transplantation, yet the underlying mechanisms were not fully understood. Sentrin‐specific protease 1 (SENP1) is an important member of the SENP family, which is widely involved in various diseases. However, the role of SENP1 in RIRI has been unclear. In our study, we discovered that SENP1 was involved in RIRI and reduced renal cell apoptosis and oxidative stress at elevated levels. Further mechanistic studies showed that hypoxia‐inducible factor‐1α (HIF‐1α) was identified as a substrate of SENP1. Furthermore, SENP1 deSUMOylated HIF‐1α, which reduced the degradation of HIF‐1α, and exerted a renoprotective function. In addition, the protective function was lost after application of the HIF‐1α specific inhibitor KC7F2. Briefly, our results fully demonstrated that SENP1 reduced the degradation of HIF‐1α and attenuated oxidative stress and apoptosis in RIRI by regulating the deSUMOylation of HIF‐1α, suggesting that SENP1 may serve as a potential therapeutic target for the treatment of RIRI.