Beige adipocytes are an inducible form of thermogenic adipocytes that emerge in response to certain extrinsic stimuli, such as chronic cold exposure and burn injury (i.e., ?browning? of white fat), and contribute to systemic glucose homeostasis. Given its inducible nature and relevance to adult humans, beige adipocytes have gained much attention as a potential therapeutic target in type 2 diabetes. This proposal is inspired by the recent findings that human subcutaneous white adipose tissue adopts a robust browning phenotype following a severe burn injury and that human beige fat possesses high capacity to oxidize glucose, fatty acids, and branched-chain amino acids (BCAA). The current objective is to extend our understandings on the biological roles and developmental pathway of human beige adipocytes in response to burn injuries.
In Aim 1, we will test the hypothesis that the burn- induced beige fat functions as a ?metabolic sink? not only for glucose, fatty acids but also for BCAA, which contributes to the prevention of post-burn hyperglycemia.
In Aim 2, we will characterize molecular signatures of the burn-induced beige adipocytes at single-cell resolution and determine its developmental pathway. Our findings will have a significant impact because by use of the ?burn model? we will determine the functional roles of WAT browning in the regulation of systemic glucose homeostasis and insulin resistance in humans. Our study will also develop the innovative concept that BAT is not simply a heat-generating organ but can also function as a metabolic sink for glucose, fatty acid, and BCAA.

Public Health Relevance

Rodents and humans possess beige adipocytes, an inducible form of thermogenic adipocytes that emerge in response to chronic cold exposure and severe burn injury. By use of the ?burn model? as a unique example of human beige fat, our research will define the biological roles and developmental pathway of human beige adipocytes with a special emphasis on its role as a metabolic sink for glucose, fatty acids, and branched chain amino acids.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK112268-02
Application #
9354485
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Haft, Carol R
Project Start
2016-09-20
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2019-06-30
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Anatomy/Cell Biology
Type
Schools of Dentistry/Oral Hygn
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
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Mills, Evanna L; Pierce, Kerry A; Jedrychowski, Mark P et al. (2018) Accumulation of succinate controls activation of adipose tissue thermogenesis. Nature 560:102-106
Chondronikola, Maria; Volpi, Elena; Børsheim, Elisabet et al. (2016) Brown Adipose Tissue Activation Is Linked to Distinct Systemic Effects on Lipid Metabolism in Humans. Cell Metab 23:1200-1206