神经干细胞
蛋白质稳态
干细胞
溶酶体
细胞生物学
干细胞衰老理论
生物
自噬
神经科学
干细胞因子
祖细胞
生物化学
细胞凋亡
酶
作者
Dena S. Leeman,Katja Hebestreit,Tyson Joel Ruetz,Ashley E. Webb,Andrew S. McKay,Elizabeth A. Pollina,Ben W. Dulken,Xiaoai Zhao,Robin W. Yeo,Theodore T. Ho,Salah Mahmoudi,Keerthana Devarajan,Emmanuelle A. Passegue,Thomas A. Rando,Judith Frydman,Anne Brunet
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-03-15
卷期号:359 (6381): 1277-1283
被引量:527
标识
DOI:10.1126/science.aag3048
摘要
In the adult brain, the neural stem cell (NSC) pool comprises quiescent and activated populations with distinct roles. Transcriptomic analysis revealed that quiescent and activated NSCs exhibited differences in their protein homeostasis network. Whereas activated NSCs had active proteasomes, quiescent NSCs contained large lysosomes. Quiescent NSCs from young mice accumulated protein aggregates, and many of these aggregates were stored in large lysosomes. Perturbation of lysosomal activity in quiescent NSCs affected protein-aggregate accumulation and the ability of quiescent NSCs to activate. During aging, quiescent NSCs displayed defects in their lysosomes, increased accumulation of protein aggregates, and reduced ability to activate. Enhancement of the lysosome pathway in old quiescent NSCs cleared protein aggregates and ameliorated the ability of quiescent NSCs to activate, allowing them to regain a more youthful state.
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