Back to Search Start Over

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

Authors :
Yu B
Battaglia DM
Foster TP
Nichols CD
Source :
Scientific reports [Sci Rep] 2021 Oct 05; Vol. 11 (1), pp. 19714. Date of Electronic Publication: 2021 Oct 05.
Publication Year :
2021

Abstract

Serotonin 5-HT <subscript>2</subscript> receptors are expressed in many tissues and play important roles in biological processes. Although the 5-HT <subscript>2A</subscript> receptor is primarily known for its role in central nervous system, it is also expressed in peripheral tissues. We have found that 5-HT <subscript>2A</subscript> receptor antagonists inhibit human subcutaneous primary adipocyte differentiation. We also show that siRNA knockdown of the 5-HT <subscript>2A</subscript> receptor blocks differentiation. Using gene expression analysis in combination with receptor antagonists we found that activity of 5-HT <subscript>2A</subscript> 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 <subscript>2A</subscript> receptor activity is necessary for differentiation of human primary subcutaneous preadipocytes to adipocytes, and that 5-HT <subscript>2A</subscript> 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 <subscript>2A</subscript> 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.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2045-2322
Volume :
11
Issue :
1
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
34611182
Full Text :
https://doi.org/10.1038/s41598-021-98970-1