Let-7 Coordinately Suppresses Components of the Amino Acid Sensing Pathway to Repress mTORC1 and Induce Autophagy

被引:71
作者
Dubinsky, Amy N. [1 ]
Dastidar, Somasish Ghosh [1 ]
Hsu, Cynthia L. [1 ]
Zahra, Rabaab [1 ]
Djakovic, Stevan N. [1 ]
Duarte, Sonia [8 ]
Esau, Christine C.
Spencer, Brian [2 ]
Ashe, Travis D. [1 ]
Fischer, Kimberlee M. [10 ]
MacKenna, Deidre A. [10 ]
Sopher, Bryce L. [11 ]
Masliah, Eliezer [2 ]
Gaasterland, Terry [5 ]
Chau, B. Nelson [10 ]
de Almeida, Luis Pereira [8 ,9 ]
Morrison, Bradley E. [1 ]
La Spada, Albert R. [1 ,2 ,3 ,4 ,6 ,7 ,12 ]
机构
[1] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Div Biol Sci, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[7] Univ Calif San Diego, Sanford Consortium Regenerat Med, La Jolla, CA 92093 USA
[8] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, P-3004517 Coimbra, Portugal
[9] Univ Coimbra, Fac Pharm, P-3000548 Coimbra, Portugal
[10] Regulus Therapeut, San Diego, CA 92121 USA
[11] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[12] Rady Childrens Hosp, San Diego, CA 92123 USA
关键词
RAG GTPASES; REGULATES MTOR; MOUSE MODELS; PROTEIN; INHIBITION; METABOLISM; MICRORNAS; RAGULATOR; LYSOSOME; TARGET;
D O I
10.1016/j.cmet.2014.09.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macroautophagy (hereafter autophagy) is the major pathway by which macromolecules and organelles are degraded. Autophagy is regulated by the mTOR signaling pathway-the focal point for integration of metabolic information, with mTORC1 playing a central role in balancing biosynthesis and catabolism. Of the various inputs to mTORC1, the amino acid sensing pathway is among the most potent. Based upon transcriptome analysis of neurons subjected to nutrient deprivation, we identified let-7 microRNA as capable of promoting neuronal autophagy. We found that let-7 activates autophagy by coordinately down-regulating the amino acid sensing pathway to prevent mTORC1 activation. Let-7 induced autophagy in the brain to eliminate protein aggregates, establishing its physiological relevance for in vivo autophagy modulation. Moreover, peripheral delivery of let-7 anti-miR repressed autophagy in muscle and white fat, suggesting that let-7 autophagy regulation extends beyond CNS. Hence, let-7 plays a central role in nutrient homeostasis and proteostasis regulation in higher organisms.
引用
收藏
页码:626 / 638
页数:13
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