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Silencing of hypothalamic FGF11 prevents diet-induced obesity

Fibroblast growth factor 11 (FGF11) is a member of the intracellular fibroblast growth factor family. Here, we report the central role of FGF11 in the regulation of metabolism. Lentiviral injection of Fgf11 shRNA into the arcuate nucleus of the mouse hypothalamus decreased weight gain and fat mass,...

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Autores principales: Cho, Jae Hyun, Kim, Kyungchan, Cho, Han Chae, Lee, Jaemeun, Kim, Eun-Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9447329/
https://www.ncbi.nlm.nih.gov/pubmed/36064426
http://dx.doi.org/10.1186/s13041-022-00962-3
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author Cho, Jae Hyun
Kim, Kyungchan
Cho, Han Chae
Lee, Jaemeun
Kim, Eun-Kyoung
author_facet Cho, Jae Hyun
Kim, Kyungchan
Cho, Han Chae
Lee, Jaemeun
Kim, Eun-Kyoung
author_sort Cho, Jae Hyun
collection PubMed
description Fibroblast growth factor 11 (FGF11) is a member of the intracellular fibroblast growth factor family. Here, we report the central role of FGF11 in the regulation of metabolism. Lentiviral injection of Fgf11 shRNA into the arcuate nucleus of the mouse hypothalamus decreased weight gain and fat mass, increased brown adipose tissue thermogenesis, and improved glucose and insulin intolerances under high-fat diet conditions. Fgf11 was expressed in the NPY–expressing neurons, and Fgf11 knockdown considerably decreased Npy expression and projection, leading to increased expression of tyrosine hydroxylase in the paraventricular nucleus. Mechanistically, FGF11 regulated Npy gene expression through the glycogen synthase kinase 3–cAMP response element-binding protein pathway. Our study defines the physiological significance of hypothalamic FGF11 in the regulation of metabolism in response to overnutrition such as high-fat diet. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00962-3.
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spelling pubmed-94473292022-09-07 Silencing of hypothalamic FGF11 prevents diet-induced obesity Cho, Jae Hyun Kim, Kyungchan Cho, Han Chae Lee, Jaemeun Kim, Eun-Kyoung Mol Brain Research Fibroblast growth factor 11 (FGF11) is a member of the intracellular fibroblast growth factor family. Here, we report the central role of FGF11 in the regulation of metabolism. Lentiviral injection of Fgf11 shRNA into the arcuate nucleus of the mouse hypothalamus decreased weight gain and fat mass, increased brown adipose tissue thermogenesis, and improved glucose and insulin intolerances under high-fat diet conditions. Fgf11 was expressed in the NPY–expressing neurons, and Fgf11 knockdown considerably decreased Npy expression and projection, leading to increased expression of tyrosine hydroxylase in the paraventricular nucleus. Mechanistically, FGF11 regulated Npy gene expression through the glycogen synthase kinase 3–cAMP response element-binding protein pathway. Our study defines the physiological significance of hypothalamic FGF11 in the regulation of metabolism in response to overnutrition such as high-fat diet. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00962-3. BioMed Central 2022-09-05 /pmc/articles/PMC9447329/ /pubmed/36064426 http://dx.doi.org/10.1186/s13041-022-00962-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cho, Jae Hyun
Kim, Kyungchan
Cho, Han Chae
Lee, Jaemeun
Kim, Eun-Kyoung
Silencing of hypothalamic FGF11 prevents diet-induced obesity
title Silencing of hypothalamic FGF11 prevents diet-induced obesity
title_full Silencing of hypothalamic FGF11 prevents diet-induced obesity
title_fullStr Silencing of hypothalamic FGF11 prevents diet-induced obesity
title_full_unstemmed Silencing of hypothalamic FGF11 prevents diet-induced obesity
title_short Silencing of hypothalamic FGF11 prevents diet-induced obesity
title_sort silencing of hypothalamic fgf11 prevents diet-induced obesity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9447329/
https://www.ncbi.nlm.nih.gov/pubmed/36064426
http://dx.doi.org/10.1186/s13041-022-00962-3
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