| Literature DB >> 31914697 |
Meiting Xue1,2,3, Yue Shi1, Aiming Pang4, Li Men1, Yahui Hu1, Pengfei Zhou1, Guangfeng Long1, Xin Tian1, Rong Wang1, Yonghua Zhao5, Xudong Liao6, Yanna Shen1, Yujie Cui1.
Abstract
Diabetic nephropathy (DN) is one of the leading causes of mortality in diabetic patients, but its pathogenesis is unclear. We aimed to study the role of the pro-ANP convertase Corin in the pathogenesis of DN. Corin and ANP expression in DN rat kidneys and high-glucose-treated HK-2 cells was analyzed by real-time PCR, western blotting, and immunohistochemical staining. The effect of Corin-siRNA or ANP-siRNA HK-2 cells on EA.hy926 cell migration was determined by scratch-wound healing assay. The expression of mitogen-activated protein kinase (MAPK) and endothelial NO synthase (eNOS) in EA.hy926 cells treated with conditioned medium from Corin-siRNA- or ANP-siRNA-transfected HK-2 cells was determined by western blotting. We found a significant reduction in Corin and ANP expression in DN rat kidneys. These results were recapitulated in HK-2 cells treated with high glucose. EA.hy926 cells treated with conditioned medium from Corin-deficient HK-2 cells had inhibited migration, increased MAPK activity, and decreased eNOS activity. Similar effects were observed with ANP-siRNA transfection. Finally, adding ANP to the Corin-deficient HK-2 conditioned medium rescued the above defects, indicating that Corin mediates its effects through ANP. In conclusion, Corin plays a renoprotective role through pro-ANP processing, and defects in Corin cause endothelial dysfunction through MAPK and eNOS signaling in DN.Entities:
Keywords: Corin; MAPK; diabetic nephropathy; eNOS; endothelial dysfunction
Year: 2019 PMID: 31914697 DOI: 10.1096/fj.201900531RR
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191