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Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression

Serotonin 5-HT(2) receptors are expressed in many tissues and play important roles in biological processes. Although the 5-HT(2A) receptor is primarily known for its role in central nervous system, it is also expressed in peripheral tissues. We have found that 5-HT(2A) receptor antagonists inhibit h...

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Autores principales: Yu, Bangning, Battaglia, Diana M., Foster, Timothy P., Nichols, Charles D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492876/
https://www.ncbi.nlm.nih.gov/pubmed/34611182
http://dx.doi.org/10.1038/s41598-021-98970-1
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author Yu, Bangning
Battaglia, Diana M.
Foster, Timothy P.
Nichols, Charles D.
author_facet Yu, Bangning
Battaglia, Diana M.
Foster, Timothy P.
Nichols, Charles D.
author_sort Yu, Bangning
collection PubMed
description Serotonin 5-HT(2) receptors are expressed in many tissues and play important roles in biological processes. Although the 5-HT(2A) receptor is primarily known for its role in central nervous system, it is also expressed in peripheral tissues. We have found that 5-HT(2A) receptor antagonists inhibit human subcutaneous primary adipocyte differentiation. We also show that siRNA knockdown of the 5-HT(2A) receptor blocks differentiation. Using gene expression analysis in combination with receptor antagonists we found that activity of 5-HT(2A) receptors is necessary very early in the differentiation process to mediate expression of adipogenic genes, including peroxisome proliferator-activated receptor gamma (ppar-γ), adipocyte protein 2 (aP2), adiponectin, and serine/threonine-protein kinase 1 (sgk1). We show here for the first time that 5-HT(2A) receptor activity is necessary for differentiation of human primary subcutaneous preadipocytes to adipocytes, and that 5-HT(2A) receptor activity mediates key genes related to adipogenesis during this process. Importantly, this work contributes to a greater understanding of the adipocyte differentiation process, as well as to the role of 5-HT(2A) receptors in peripheral tissues, and may be relevant to the development of novel therapeutic strategies targeting this receptor for the treatment of obesity related diseases.
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spelling pubmed-84928762021-10-07 Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression Yu, Bangning Battaglia, Diana M. Foster, Timothy P. Nichols, Charles D. Sci Rep Article Serotonin 5-HT(2) receptors are expressed in many tissues and play important roles in biological processes. Although the 5-HT(2A) receptor is primarily known for its role in central nervous system, it is also expressed in peripheral tissues. We have found that 5-HT(2A) receptor antagonists inhibit human subcutaneous primary adipocyte differentiation. We also show that siRNA knockdown of the 5-HT(2A) receptor blocks differentiation. Using gene expression analysis in combination with receptor antagonists we found that activity of 5-HT(2A) receptors is necessary very early in the differentiation process to mediate expression of adipogenic genes, including peroxisome proliferator-activated receptor gamma (ppar-γ), adipocyte protein 2 (aP2), adiponectin, and serine/threonine-protein kinase 1 (sgk1). We show here for the first time that 5-HT(2A) receptor activity is necessary for differentiation of human primary subcutaneous preadipocytes to adipocytes, and that 5-HT(2A) receptor activity mediates key genes related to adipogenesis during this process. Importantly, this work contributes to a greater understanding of the adipocyte differentiation process, as well as to the role of 5-HT(2A) receptors in peripheral tissues, and may be relevant to the development of novel therapeutic strategies targeting this receptor for the treatment of obesity related diseases. Nature Publishing Group UK 2021-10-05 /pmc/articles/PMC8492876/ /pubmed/34611182 http://dx.doi.org/10.1038/s41598-021-98970-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Yu, Bangning
Battaglia, Diana M.
Foster, Timothy P.
Nichols, Charles D.
Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title_full Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title_fullStr Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title_full_unstemmed Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title_short Serotonin 5-HT(2A) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
title_sort serotonin 5-ht(2a) receptor activity mediates adipocyte differentiation through control of adipogenic gene expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492876/
https://www.ncbi.nlm.nih.gov/pubmed/34611182
http://dx.doi.org/10.1038/s41598-021-98970-1
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