自噬
安普克
细胞生物学
代谢途径
mTORC1型
信号转导
代谢组学
生物
PI3K/AKT/mTOR通路
ULK1
新陈代谢
化学
蛋白激酶A
生物化学
激酶
生物信息学
细胞凋亡
作者
Alexander S. Häusl,Thomas Bajaj,Lea M. Brix,Max L. Pöhlmann,Kathrin Hafner,Meri De Angelis,Joachim Nagler,Frederik Dethloff,Georgia Balsevich,Karl‐Werner Schramm,Patrick Giavalisco,Alon Chen,Mathias V. Schmidt,Nils C. Gassen
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2022-03-09
卷期号:8 (10)
被引量:15
标识
DOI:10.1126/sciadv.abi4797
摘要
The mediobasal hypothalamus (MBH) is the central region in the physiological response to metabolic stress. The FK506-binding protein 51 (FKBP51) is a major modulator of the stress response and has recently emerged as a scaffolder regulating metabolic and autophagy pathways. However, the detailed protein-protein interactions linking FKBP51 to autophagy upon metabolic challenges remain elusive. We performed mass spectrometry-based metabolomics of FKBP51 knockout (KO) cells revealing an increased amino acid and polyamine metabolism. We identified FKBP51 as a central nexus for the recruitment of the LKB1/AMPK complex to WIPI4 and TSC2 to WIPI3, thereby regulating the balance between autophagy and mTOR signaling in response to metabolic challenges. Furthermore, we demonstrated that MBH FKBP51 deletion strongly induces obesity, while its overexpression protects against high-fat diet (HFD)-induced obesity. Our study provides an important novel regulatory function of MBH FKBP51 within the stress-adapted autophagy response to metabolic challenges.
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