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  Mediobasal hypothalamic FKBP51 acts as a molecular switch linking autophagy to whole-body metabolism

Hausl, A. S., Bajaj, T., Brix, L., Pohlmann, M. L., Hafner, K., De Angelis, M., et al. (2022). Mediobasal hypothalamic FKBP51 acts as a molecular switch linking autophagy to whole-body metabolism. SCIENCE ADVANCES, 8(10): eabi4797. doi:10.1126/sciadv.abi4797.

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Hausl, Alexander S.1, Autor           
Bajaj, Thomas, Autor
Brix, Lea1, 2, Autor           
Pohlmann, Max L.1, Autor           
Hafner, Kathrin3, Autor           
De Angelis, Meri, Autor
Nagler, Joachim, Autor
Dethloff, Frederik, Autor
Balsevich, Georgia1, Autor           
Schramm, Karl-Werner, Autor
Giavalisco, Patrick, Autor
Chen, Alon4, Autor           
Schmidt, Mathias V.1, Autor           
Gassen, Nils C.3, Autor           
Affiliations:
1RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society, ou_2040294              
2IMPRS Translational Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_3318616              
3Dept. Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              
4Dept. Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035294              

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 Zusammenfassung: 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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 Datum: 2022
 Publikationsstatus: Online veröffentlicht
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 Identifikatoren: ISI: 000766438000018
DOI: 10.1126/sciadv.abi4797
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Titel: SCIENCE ADVANCES
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 8 (10) Artikelnummer: eabi4797 Start- / Endseite: - Identifikator: ISSN: 2375-2548