| Literature DB >> 30332637 |
Paul Petrus1, Niklas Mejhert1, Patricia Corrales2, Simon Lecoutre1, Qian Li1, Estela Maldonado3, Agne Kulyté1, Yamila Lopez2, Mark Campbell4, Juan R Acosta1, Jurga Laurencikiene1, Iyadh Douagi1, Hui Gao5, Concepción Martínez-Álvarez3, Per Hedén6, Kirsty L Spalding1, Antonio Vidal-Puig4, Gema Medina-Gomez7, Peter Arner1, Mikael Rydén8.
Abstract
White adipose tissue (WAT) mass is determined by adipocyte size and number. While adipocytes are continuously turned over, the mechanisms controlling fat cell number in WAT upon weight changes are unclear. Herein, prospective studies of human subcutaneous WAT demonstrate that weight gain increases both adipocyte size and number, but the latter remains unaltered after weight loss. Transcriptome analyses associate changes in adipocyte number with the expression of 79 genes. This gene set is enriched for growth factors, out of which one, transforming growth factor-β3 (TGFβ3), stimulates adipocyte progenitor proliferation, resulting in a higher number of cells undergoing differentiation in vitro. The relevance of these observations was corroborated in vivo where Tgfb3+/- mice, in comparison with wild-type littermates, display lower subcutaneous adipocyte progenitor proliferation, WAT hypertrophy, and glucose intolerance. TGFβ3 is therefore a regulator of subcutaneous adipocyte number and may link WAT morphology to glucose metabolism.Entities:
Keywords: adipogenesis; cellularity; glucose tolerance; growth factor; obesity
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Year: 2018 PMID: 30332637 DOI: 10.1016/j.celrep.2018.09.069
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423