Built to last: lysosome remodeling and repair in health and disease

被引:37
|
作者
Zoncu, Roberto [1 ,2 ]
Perera, Rushika M. [3 ,4 ,5 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cellular Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Innovat Genom Inst, Berkeley, CA 94720 USA
[3] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
CELLULAR LIPID-METABOLISM; TRANSCRIPTIONAL ACTIVITY; FRONTOTEMPORAL DEMENTIA; CYSTEINE CATHEPSINS; DAMAGED LYSOSOMES; MEMBRANE REPAIR; CANCER; AUTOPHAGY; TFEB; BIOGENESIS;
D O I
10.1016/j.tcb.2021.12.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lysosomes play major roles in growth regulation and catabolism and are recognized as critical mediators of cellular remodeling. An emerging theme is how the lysosome is itself subjected to extensive remodeling in order to perform specific tasks that meet the changing demands of the cell. Accordingly, lysosomes can sustain physical damage and undergo dramatic changes in composition following pathogen infection, accumulation of protein aggregates, or cellular transformation, necessitating dedicated pathways for their repair, remodeling, and restoration. In this review, we focus on emerging molecular mechanisms for piecemeal remodeling of lysosomal components and wholesale repair and discuss their implications in physiological and pathogenic challenges such as cancer, neurodegeneration, and pathogen infection.
引用
收藏
页码:597 / 610
页数:14
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