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Transforming Growth Factor-β3 Regulates Adipocyte Number in Subcutaneous White Adipose Tissue
Author(s) -
Paul Petrus,
Niklas Mejhert,
Patricia Corrales,
Simon Lecoutre,
Qian Li,
Estela Maldonado,
Agné Kulyté,
Yamila López,
Mark Campbell,
Juan R. Acosta,
Jurga Laurencikiene,
Iyadh Douagi,
Hui Gao,
Concepción MartínezÁlvarez,
Per Hedén,
Kirsty L. Spalding,
António Vidal-Puig,
Gema MedinaGómez,
Peter Arner,
Mikael Rydén
Publication year - 2018
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2018.09.069
Subject(s) - adipocyte , adipose tissue , white adipose tissue , subcutaneous adipose tissue , subcutaneous fat , medicine , growth factor , transforming growth factor , endocrinology , subcutaneous tissue , white (mutation) , microbiology and biotechnology , biology , pathology , receptor , genetics , gene
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.

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