Department of Pediatrics, Jinling Hospital, The first school of clinical Medicine, Southern Medical University, Nanjing, P. R. China.
Department of Pediatrics, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, P. R. China.
J Recept Signal Transduct Res. 2020 Jun;40(3):273-280. doi: 10.1080/10799893.2020.1731536. Epub 2020 Feb 26.
The aim of our study is to investigate the relationship between podocyte autophagy and apoptosis induced by Puromycin Aminonucleoside (PAN) and to clarify its mechanism. Podocytes were cultured . The apoptosis rates of each group were detected using flow cytometry. The expression of LC3-II protein and changes in distribution were detected through laser scanning confocal microscope, and the western blot protocol was employed for detection of protein expression of LC3-II. The autophagosomes were detected by transmission electron microscopy. In this study, We found that autophagosome increased followed by apoptosis after podocyte injury. Furthermore, we conformed that the activation of autophagy could inhibit the apoptosis to alleviate the injury of podocyte at an early stage. Autophagy occurred earlier before apoptosis and autophagy mediated podocyte apoptosis induced by PAN. These findings indicate that autophagy may become a novel therapeutic target for the treatment of podocyte injury and proteinuria in the future.
本研究旨在探讨嘌呤霉素氨基核苷(PAN)诱导的足细胞自噬和凋亡之间的关系,并阐明其机制。将足细胞进行培养。采用流式细胞术检测各组细胞的凋亡率。激光共聚焦显微镜检测 LC3-II 蛋白的表达及分布变化,Western blot 法检测 LC3-II 蛋白的表达。透射电镜观察自噬小体。本研究发现,足细胞损伤后自噬体增加,随后发生凋亡。此外,我们证实自噬的激活可以抑制凋亡,从而减轻早期足细胞的损伤。自噬发生在凋亡之前,自噬介导了 PAN 诱导的足细胞凋亡。这些发现表明,自噬可能成为未来治疗足细胞损伤和蛋白尿的新靶点。