Resistin/Fizz3 expression in relation to obesity and peroxisome proliferator-activated receptor-γ action in humans

被引:616
作者
Savage, DB
Sewter, CP
Klenk, ES
Segal, DG
Vidal-Puig, A
Considine, RV
O'Rahilly, S
机构
[1] Addenbrookes Hosp, Dept Med, Cambridge CB2 2QR, England
[2] Addenbrookes Hosp, Dept Clin Biochem, Cambridge CB2 2QR, England
[3] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46204 USA
关键词
D O I
10.2337/diabetes.50.10.2199
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent studies in murine models suggest that resistin (also called Fizz3 [1]), a novel cysteine-rich protein secreted by adipocytes, may represent the long-sought link between obesity and insulin resistance (2). Furthermore, peroxisome proliferator-activated receptor-gamma, (PPAR-gamma) agonists appear to inhibit resistin expression in murine adipocytes, providing a possible explanation for the mode of action of this class of insulin sensitizers (2). Using a fluorescent real-time reverse transcriptase-polymerase chain reaction-based assay, we found that resistin mRNA levels in whole adipose tissue samples were increased in morbidly obese humans compared with lean control subjects. However, in freshly isolated human adipocytes, resistin mRNA levels were very low and showed no correlation with BMI. Resistin mRNA was undetectable in preadipocytes, endothelial cells, and vascular smooth muscle cells, but it was readily detectable in circulating mononuclear cells. Although exposure of human mononuclear cells to PPAR-gamma agonists markedly upregulated fatty acid-binding protein-4 expression, these agents had no effect on mononuclear cell resistin expression. Finally, resistin mRNA was undetectable in adipocytes from a severely insulin-resistant subject with a dominant-negative mutation in PPAR-gamma (3). We conclude that the recently described relationships of murine resistin/Fizz3 expression with obesity, insulin resistance, and PPAR-gamma action may not readily translate to humans. Further studies of this novel class of proteins are needed to clarify their roles in human metabolism.
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页码:2199 / 2202
页数:4
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