Limitation of adipose tissue by the number of embryonic progenitor cells

Author:

Hedbacker Kristina12ORCID,Lu Yi-Hsueh1,Dallner Olof1ORCID,Li Zhiying1ORCID,Fayzikhodjaeva Gulya12,Birsoy Kıvanç13,Han Chiayun4,Yang Chingwen4,Friedman Jeffrey M12ORCID

Affiliation:

1. Laboratory of Molecular Genetics, The Rockefeller University, New York, United States

2. Howard Hughes Medical Institute, The Rockefeller University, New York, United States

3. Laboratory of Metabolic Regulation and Genetics, The Rockefeller University, New York, United States

4. Gene Targeting Resource Center, The Rockefeller University, New York, United States

Abstract

Adipogenesis in adulthood replaces fat cells that turn over and can contribute to the development of obesity. However, the proliferative potential of adipocyte progenitors in vivo is unknown (Faust et al., 1976; Faust et al., 1977; Hirsch and Han, 1969; Johnson and Hirsch, 1972). We addressed this by injecting labeled wild-type embryonic stem cells into blastocysts derived from lipodystrophic A-ZIP transgenic mice, which have a genetic block in adipogenesis. In the resulting chimeric animals, wild-type ES cells are the only source of mature adipocytes. We found that when chimeric animals were fed a high-fat-diet, animals with low levels of chimerism showed a significantly lower adipose tissue mass than animals with high levels of chimerism. The difference in adipose tissue mass was attributed to variability in the amount of subcutaneous adipose tissue as the amount of visceral fat was independent of the level of chimerism. Our findings thus suggest that proliferative potential of adipocyte precursors is limited and can restrain the development of obesity.

Funder

JPB Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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