Proteotoxic stress disrupts epithelial integrity by inducing MTOR sequestration and autophagy overactivation

自噬 细胞生物学 生物 蛋白质稳态 PI3K/AKT/mTOR通路 袋3 内体 自噬体 灯1 细胞内 信号转导 生物化学 细胞凋亡
作者
Xiaoxiang Cheng,Pei Zhang,Hongyu Zhao,Hui Zheng,Kai Zheng,Hong Zhao,Hongjie Zhang
出处
期刊:Autophagy [Taylor & Francis]
卷期号:19 (1): 241-255 被引量:1
标识
DOI:10.1080/15548627.2022.2071381
摘要

Macroautophagy/autophagy, an evolutionarily conserved degradation system, serves to clear intracellular components through the lysosomal pathway. Mounting evidence has revealed cytoprotective roles of autophagy; however, the intracellular causes of overactivated autophagy, which has cytotoxic effects, remain elusive. Here we show that sustained proteotoxic stress induced by loss of the RING and Kelch repeat-containing protein C53A5.6/RIKE-1 induces sequestration of LET-363/MTOR complex and overactivation of autophagy, and consequently impairs epithelial integrity in C. elegans. In C53A5.6/RIKE-1-deficient animals, blocking autophagosome formation effectively prevents excessive endosomal degradation, mitigates mislocalization of intestinal membrane components and restores intestinal lumen morphology. However, autophagy inhibition does not affect LET-363/MTOR aggregation in animals with compromised C53A5.6/RIKE-1 function. Improving proteostasis capacity by reducing DAF-2 insulin/IGF1 signaling markedly relieves the aggregation of LET-363/MTOR and alleviates autophagy overactivation, which in turn reverses derailed endosomal trafficking and rescues epithelial morphogenesis defects in C53A5.6/RIKE-1-deficient animals. Hence, our studies reveal that C53A5.6/RIKE-1-mediated proteostasis is critical for maintaining the basal level of autophagy and epithelial integrity.Abbreviations: ACT-5: actin 5; ACTB: actin beta; ALs: autolysosomes; APs: autophagosomes; AJM-1: apical junction molecule; ATG: autophagy related; C. elegans: Caenorhabditis elegans; CPL-1: cathepsin L family; DAF: abnormal dauer formation; DLG-1: Drosophila discs large homolog; ERM-1: ezrin/radixin/moesin; EPG: ectopic P granule; GFP: freen fluorescent protein; HLH-30: helix loop helix; HSP: heat shock protein; LAAT-1: lysosome associated amino acid transporter; LET: lethal; LGG-1: LC3, GABARAP and GATE-16 family; LMP-1: LAMP (lysosome-associated membrane protein) homolog; MTOR: mechanistic target of rapamycin kinase; NUC-1: abnormal nuclease; PEPT-1/OPT-2: Peptide transporter family; PGP-1: P-glycoprotein related; RAB: RAB family; RIKE-1: RING and Kelch repeat-containing protein; SLCF-1: solute carrier family; SQST-1: sequestosome related; SPTL-1: serine palmitoyl transferase family.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
2秒前
隐形曼青应助结实的山菡采纳,获得30
4秒前
Can完成签到 ,获得积分10
4秒前
颜琀樱发布了新的文献求助10
4秒前
sy发布了新的文献求助10
5秒前
6秒前
6秒前
6秒前
明良韵发布了新的文献求助10
7秒前
7秒前
英姑应助一一采纳,获得10
7秒前
7秒前
7秒前
10秒前
10秒前
小马甲应助nuo采纳,获得10
11秒前
Orange应助Shelley采纳,获得10
11秒前
年轻月饼完成签到 ,获得积分10
11秒前
12秒前
12秒前
此晴可待发布了新的文献求助10
12秒前
追寻芷发布了新的文献求助10
12秒前
领导范儿应助111采纳,获得10
13秒前
14秒前
link咩发布了新的文献求助30
14秒前
彩色淼淼完成签到,获得积分10
14秒前
huanggaga发布了新的文献求助10
14秒前
zz发布了新的文献求助10
15秒前
你好发布了新的文献求助10
15秒前
Can关注了科研通微信公众号
15秒前
16秒前
幸福无声发布了新的文献求助10
16秒前
16秒前
三家分晋发布了新的文献求助10
17秒前
17秒前
17秒前
17秒前
梓镱儿完成签到,获得积分10
21秒前
轻松书白发布了新的文献求助10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Principles of town planning: translating concepts to applications 1000
内視鏡的に摘除しえた十二指腸乳頭部腫瘍の2例 660
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Interpolation and Regression Models for the Chemical Engineer: Solving Numerical Problems 400
The Neuroscience of Language 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7687110
求助须知:如何正确求助?哪些是违规求助? 9250182
关于积分的说明 19961469
捐赠科研通 7260139
什么是DOI,文献DOI怎么找? 3289721
关于科研通互助平台的介绍 2446647
邀请新用户注册赠送积分活动 2294249