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  Contribution of the co-chaperone FKBP51 in the ventromedial hypothalamus to metabolic homeostasis in male and female mice

Brix, L., Toksöz, I., Aman, L., Kovarova, V., Springer, M., Bordes, J., et al. (2022). Contribution of the co-chaperone FKBP51 in the ventromedial hypothalamus to metabolic homeostasis in male and female mice. MOLECULAR METABOLISM, 65: 101579. doi:10.1016/j.molmet.2022.101579.

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 Creators:
Brix, Lea1, 2, Author           
Toksöz, Irmak1, Author           
Aman, London1, Author           
Kovarova, Veronika1, Author           
Springer, Margherita1, Author           
Bordes, Joeri1, 2, Author           
van Doeselaar, Lotte1, 2, Author           
Engelhardt, Clara1, Author           
Haeusl, Alexander S1, Author           
Narayan, Sowmya1, 2, Author           
Sterlemann, Vera3, Author           
Yang, Huanqing1, Author           
Deussing, Jan M.4, Author           
Schmidt, Mathias V.1, Author           
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              
3Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137              
4RG Molecular Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society, ou_2040293              

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 Abstract: Objective: Steroidogenic factor 1 (SF1) expressing neurons in the ventromedial hypothalamus (VMH) have been directly implicated in whole-body metabolism and in the onset of obesity. The co-chaperone FKBP51 is abundantly expressed in the VMH and was recently linked to type 2 diabetes, insulin resistance, adipogenesis, browning of white adipose tissue (WAT) and bodyweight regulation.
Methods: We investigated the role of FKBP51 in the VMH by conditional deletion and virus-mediated overexpression of FKBP51 in SF1-positive neurons. Baseline and high fat diet (HFD)-induced metabolic- and stress-related phenotypes in male and female mice were obtained.
Results: In contrast to previously reported robust phenotypes of FKBP51 manipulation in the entire mediobasal hypothalamus (MBH), selective deletion or overexpression of FKBP51 in the VMH resulted in only a moderate alteration of HFD-induced bodyweight gain and body composition, independent of sex.
Conclusions: Overall, this study shows that animals lacking and overexpressing Fkbp5 in Sf1-expressing cells within the VMH display only a mild metabolic phenotype compared to an MBH-wide manipulation of this gene, suggesting that FKBP51 in SF1 neurons within this hypothalamic nucleus plays a subsidiary role in controlling whole-body metabolism. (c) 2022 The Author(s). Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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 Dates: 2022
 Publication Status: Published online
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Title: MOLECULAR METABOLISM
Source Genre: Journal
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Pages: - Volume / Issue: 65 Sequence Number: 101579 Start / End Page: - Identifier: ISSN: 2212-8778