Distinct developmental signatures of human abdominal and gluteal subcutaneous adipose tissue depots

Kalypso Karastergiou, Susan K. Fried, Hui Xie, Mi Jeong Lee, Adeline Divoux, Marcus A. Rosencrantz, R. Jeffrey Chang, Steven R. Smith

Research output: Contribution to journalArticlepeer-review

131 Scopus citations

Abstract

Context: Fat distribution differs in men and women, but in both sexes, a predominantly glutealfemoral compared with abdominal (central) fat distribution is associated with lower metabolic risk. Differences in cellular characteristics and metabolic functions of these depots have been described, but the molecular mechanisms involved are not understood. Objective: Our objective was to identify depot- and sex-dependent differences in gene expression in human abdominal and gluteal sc adipose tissues. Design and Methods: Abdominal and gluteal adipose tissue aspirates were obtained from 14 premenopausal women [age 27.5 ± 7.0 yr,bodymass index (BMI) 27.3 ± 6.2kg/m2, andwaist-to-hip ratio 0.82 ± 0.04] and 21 men (age 29.7 ± 7.4 yr, BMI 27.2 ± 4.5 kg/m2, and waist-to-hip ratio 0.91 ± 0.07) and transcriptomes were analyzed using Illumina microarrays. Expression of selected genes was determined in isolated adipocytes and stromal vascular fractions from each depot, and in in vitro cultures before and after adipogenic differentiation. Results: A total of 284 genes were differentially expressed between the abdominal and gluteal depot, either specifically in males (n = 66) or females (n = 159) or in both sexes (n = 59). Most notably, gene ontology and pathway analysis identified homeobox genes (HOXA2, HOXA3, HOXA4, HOXA5, HOXA9, HOXB7, HOXB8, HOXC8, and IRX2) that were down-regulated in the gluteal depot in both sexes (P = 2 × 10-10). Conversely, HOXA10 was up-regulated in gluteal tissue and HOXC13 was detected exclusively in this depot. These differences were independent of BMI, were present in both adipocytes and stromal vascular fractions of adipose tissue, and were retained throughout in vitro differentiation. Conclusions: We conclude that developmentally programmed differences may contribute to the distinct phenotypic characteristics of peripheral fat.

Original languageEnglish
Pages (from-to)362-371
Number of pages10
JournalJournal of Clinical Endocrinology and Metabolism
Volume98
Issue number1
DOIs
StatePublished - Jan 2013
Externally publishedYes

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