| Literature DB >> 33591954 |
Sei Yoshida1,2, Xiaoqiong Wei1, Gensheng Zhang1, Christopher L O'Connor3, Mauricio Torres1, Zhangsen Zhou1, Liangguang Lin1, Rajasree Menon3, Xiaoxi Xu4, Wenyue Zheng2, Yi Xiong5, Edgar Otto3, Chih-Hang Anthony Tang6, Rui Hua2, Rakesh Verma3, Hiroyuki Mori1, Yang Zhang7, Chih-Chi Andrew Hu6, Ming Liu4, Puneet Garg3, Jeffrey B Hodgin8, Shengyi Sun5, Markus Bitzer3, Ling Qi1,9.
Abstract
Podocytes are key to the glomerular filtration barrier by forming a slit diaphragm between interdigitating foot processes; however, the molecular details and functional importance of protein folding and degradation in the ER remain unknown. Here, we show that the SEL1L-HRD1 protein complex of ER-associated degradation (ERAD) is required for slit diaphragm formation and glomerular filtration function. SEL1L-HRD1 ERAD is highly expressed in podocytes of both mouse and human kidneys. Mice with podocyte-specific Sel1L deficiency develop podocytopathy and severe congenital nephrotic syndrome with an impaired slit diaphragm shortly after weaning and die prematurely, with a median lifespan of approximately 3 months. We show mechanistically that nephrin, a type 1 membrane protein causally linked to congenital nephrotic syndrome, is an endogenous ERAD substrate. ERAD deficiency attenuated the maturation of nascent nephrin, leading to its retention in the ER. We also show that various autosomal-recessive nephrin disease mutants were highly unstable and broken down by SEL1L-HRD1 ERAD, which attenuated the pathogenicity of the mutants toward the WT allele. This study uncovers a critical role of SEL1L-HRD1 ERAD in glomerular filtration barrier function and provides insights into the pathogenesis associated with autosomal-recessive disease mutants.Entities:
Keywords: Cell Biology; Nephrology; Protein misfolding; Protein traffic; Ubiquitin-proteosome system
Year: 2021 PMID: 33591954 PMCID: PMC8011890 DOI: 10.1172/JCI143988
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808