The effects of temperature and seasons on subcutaneous white adipose tissue in humans: evidence for thermogenic gene induction.

TitleThe effects of temperature and seasons on subcutaneous white adipose tissue in humans: evidence for thermogenic gene induction.
Publication TypeJournal Article
Year of Publication2014
AuthorsKern PA, Finlin BS, Zhu B, Rasouli N, McGehee RE, Westgate PM, Dupont-Versteegden EE
JournalJ Clin Endocrinol Metab
Volume99
Issue12
PaginationE2772-9
Date Published2014 Dec
ISSN1945-7197
KeywordsAdipocytes, White, Adipose Tissue, White, Adult, Aged, Cells, Cultured, Energy Metabolism, Female, Humans, Insulin Resistance, Ion Channels, Male, Middle Aged, Mitochondrial Proteins, Seasons, Subcutaneous Fat, Temperature, Thermogenesis, Transcriptional Activation, Uncoupling Protein 1, Up-Regulation
Abstract

CONTEXT: Although brown adipose tissue (BAT) activity is increased by a cold environment, little is known of the response of human white adipose tissue (WAT) to the cold.

DESIGN: We examined both abdominal and thigh subcutaneous (SC) WAT from 71 subjects who were biopsied in the summer or winter, and adipose expression was assessed after an acute cold stimulus applied to the thigh of physically active young subjects.

RESULTS: In winter, UCP1 and PGC1α mRNA were increased 4 to 10-fold (p < 0.05) and 1.5 to 2-fold, respectively, along with beige adipose markers, and UCP1 protein was 3-fold higher in the winter. The seasonal increase in abdominal SC WAT UCP1 mRNA was considerably diminished in subjects with a BMI > 30 kg/m(2), suggesting that dysfunctional WAT in obesity inhibits adipose thermogenesis. After applying an acute cold stimulus to the thigh of subjects for 30 min, PGC1α and UCP1 mRNA was stimulated 2.7-fold (p < 0.05) and 1.9-fold (p = 0.07), respectively. Acute cold also induced a 2 to 3-fold increase in PGC1α and UCP1 mRNA in human adipocytes in vitro, which was inhibited by macrophage-conditioned medium and by the addition of TNFα.

CONCLUSION: Human SC WAT increases thermogenic genes seasonally and acutely in response to a cold stimulus and this response is inhibited by obesity and inflammation.

DOI10.1210/jc.2014-2440
Alternate JournalJ. Clin. Endocrinol. Metab.
PubMed ID25299843
PubMed Central IDPMC4255113
Grant ListUL1 TR000117 / TR / NCATS NIH HHS / United States
R01 DK071349 / DK / NIDDK NIH HHS / United States
UL1TR000117 / TR / NCATS NIH HHS / United States
UL1 RR033173 / RR / NCRR NIH HHS / United States
DK80327 / DK / NIDDK NIH HHS / United States
DK71349 / DK / NIDDK NIH HHS / United States
P20RR021954 / RR / NCRR NIH HHS / United States
R01 DK080327 / DK / NIDDK NIH HHS / United States
P20 RR021954 / RR / NCRR NIH HHS / United States