蛋白质稳态
秀丽隐杆线虫
自噬
激活剂(遗传学)
生物
细胞生物学
遗传学
细胞凋亡
基因
作者
Ee Phie Tan,Nora Lyang,Saam Doroodian,Pablo Sanz-Martinez,Jin Xu,Sviatlana Zaretski,José L. Nieto-Torres,Hiroshi Ebata,Shaun H. Y. Lim,William C. Hou,Khalyd J. Clay,Leonard Yoon,Lynée A. Massey,Derek Rhoades,Danny Garza,Kristen Johnson,Alan To,Lydia Ambaye,Emily P. Bentley,Michael Petrascheck
标识
DOI:10.1073/pnas.2423455122
摘要
The degradation of cellular components through autophagy is essential for longevity and healthy aging. However, autophagy function decreases with aging, contributing to age-related diseases. In this study, we characterized a small-molecule activator of autophagy called AA-20 that enhances autophagy and lipid droplet clearance in human cells and in the nematode Caenorhabditis elegans . AA-20 reduces polyglutamine aggregation in an autophagy-dependent manner in both human cells and C. elegans , where it also promotes fitness. Consistently, we found that AA-20 extends lifespan in WT C. elegans, but not in autophagy-deficient mutants. Interestingly, our findings suggest that AA-20 acts, at least in part, through a mechanism involving the transcription factor EB, but without inhibiting the protein kinase mammalian target of rapamycin complex 1. Collectively, our results identify an autophagy activator AA-20 , which may have potential therapeutic implications for aging-related proteinopathies and lipid storage disorders.
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