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Defines a Glycolytic Subpopulation and White Adipocyte Heterogeneity.

Citation
Lee, K. Y., et al. “ Defines A Glycolytic Subpopulation And White Adipocyte Heterogeneity.”. Diabetes, pp. 2822-2829.
Center Joslin Diabetes Center
Author Kevin Y Lee, Rita Sharma, Grant Gase, Siegfried Ussar, Yichao Li, Lonnie Welch, Darlene E Berryman, Andreas Kispert, Matthias Blüher, Ronald Kahn
Abstract

is a member of the T-box gene family of mesodermal developmental genes. We have recently shown that Tbx15 plays a critical role in the formation and metabolic programming of glycolytic myofibers in skeletal muscle. is also differentially expressed among white adipose tissue (WAT) in different body depots. In the current study, using three independent methods, we show that even within a single WAT depot, high expression is restricted to a subset of preadipocytes and mature white adipocytes. Gene expression and metabolic profiling demonstrate that the Tbx15 preadipocyte and adipocyte subpopulations of cells are highly glycolytic, whereas Tbx15 preadipocytes and adipocytes in the same depot are more oxidative and less glycolytic. Likewise, in humans, expression of in subcutaneous and visceral WAT is positively correlated with markers of glycolytic metabolism and inversely correlated with obesity. Furthermore, overexpression of Tbx15 is sufficient to reduce oxidative and increase glycolytic metabolism in cultured adipocytes. Thus, Tbx15 differentially regulates oxidative and glycolytic metabolism within subpopulations of white adipocytes and preadipocytes. This leads to a functional heterogeneity of cellular metabolism within WAT that has potential impact in the understanding of human metabolic diseases.

Year of Publication
2017
Journal
Diabetes
Volume
66
Issue
11
Number of Pages
2822-2829
Date Published
12/2017
ISSN Number
1939-327X
DOI
10.2337/db17-0218
Alternate Journal
Diabetes
PMID
28847884
PMCID
PMC5652605
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