Literature DB >> 29771603

Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia-reperfusion injury during initial reperfusion phase.

Xinyuan Li1,2, Gongmin Zhu1,2, Xin Gou1, Weiyang He1, Hubin Yin1,2, Xiaoyu Yang1,2, Jie Li1.   

Abstract

Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, however, have focused on the short-term effects of rapamycin administered only during the initial reperfusion phase. As such, we designed this study to explore the potential effects and mechanisms of rapamycin under a specific therapeutic regimen in which rapamycin is mixed in the perfusate during the initial reperfusion phase (within 24 h). Interestingly, we found that rapamycin maintained renal function and attenuated ischemia-reperfusion (I/R)-induced apoptosis in vivo and in vitro during the initial reperfusion phase, especially at 8 h after reperfusion. Simultaneously, rapamycin activated autophagy and inhibited endoplasmic reticulum (ER) stress and 3 pathways of unfolding protein response: ATF6, PERK, and IRE1α. Interestingly, we further found that the protective effects of rapamycin were suppressed when autophagy was inhibited by chloroquine and 3-methyladenine or when ER stress was induced by thapsigargin. Moreover, in terms of the regulatory effects of rapamycin, a negative-feedback loop between autophagy and ER stress occurred, with autophagy inhibiting ER stress and increased ER stress promoting autophagy during the initial reperfusion phase of renal I/R injury. Our study provides evidence that immediate reperfusion with rapamycin during the initial reperfusion phase repairs renal function and reduces apoptosis via activating autophagy, which could further inhibit ER stress. These results suggest a novel treatment modality for application during the initial reperfusion phase of renal I/R injury caused by kidney transplantation.-Li, X., Zhu, G., Gou, X., He, W., Yin, H., Yang, X., Li, J. Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia-reperfusion injury during initial reperfusion phase.

Entities:  

Keywords:  acute kidney injury; kidney transplantation; sirolimus

Year:  2018        PMID: 29771603     DOI: 10.1096/fj.201800299R

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  3 in total

1.  Pretreatment with Cholecalciferol Alleviates Renal Cellular Stress Response during Ischemia/Reperfusion-Induced Acute Kidney Injury.

Authors:  Jun Li; Shen Xu; Jin-Bo Zhu; Jin Song; Biao Luo; Ya-Ping Song; Zhi-Hui Zhang; Yuan-Hua Chen; Zhi-Qiang Zhang; Dong-Dong Xie; De-Xin Yu; De-Xiang Xu
Journal:  Oxid Med Cell Longev       Date:  2019-03-25       Impact factor: 6.543

2.  Mitochondrial dysfunction contributes to Rapamycin-induced apoptosis of Human Glioblastoma Cells - A synergistic effect with Temozolomide.

Authors:  Mary A Zimmerman; Samantha Wilkison; Qi Qi; Guisheng Chen; P Andy Li
Journal:  Int J Med Sci       Date:  2020-10-16       Impact factor: 3.738

3.  The relationship between endoplasmic reticulum stress and autophagy in apoptosis of BEAS-2B cells induced by cigarette smoke condensate.

Authors:  Qi Yu; Sa Yang; Zhongqiu Li; Yonghang Zhu; Zhenkai Li; Jiatong Zhang; Chunyang Li; Feifei Feng; Wei Wang; Qiao Zhang
Journal:  Toxicol Res (Camb)       Date:  2021-01-05       Impact factor: 3.524

  3 in total

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