Adiponectin gene activation by thiazolidinediones requires PPARγ2, but not C/EBPα -: evidence for differential regulation of the aP2 and adiponectin genes

被引:101
作者
Gustafson, B
Jack, MM
Cushman, SW
Smith, U [1 ]
机构
[1] Gothenburg Univ, Sahlgrenska Acad, Lundberg Lab Diabet Res, Dept Internal Med, SE-41345 Gothenburg, Sweden
[2] NIDDK, EMNS DB, NIH, Bethesda, MD 20892 USA
关键词
adiponectin; PPAR; C/EBP; transcription; cytokines; thiazolidinediones;
D O I
10.1016/S0006-291X(03)01518-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We examined the role of PPARgamma2 and C/EBPalpha for adiponectin and aP2 gene activation in C/EBPalpha(-/-) fibroblasts by stably expressing PPARgamma2 or C/EBPalpha. PPARgamma2, but not PPARgamma1, mRNA markedly increased during the differentiation to adipocytes in cells expressing C/EBPalpha. Both infected cell lines differentiated to an adipocyte phenotype and the mRNA for both aP2 and adiponectin increased in parallel. However, adiponectin mRNA was considerably higher when C/EBPalpha was present, suggesting that this transcription factor is important for full gene activation. Thiazolidinediones markedly activated the gene in PPARgamma2-expressing cells in the absence of C/EBPalpha, suggesting that the adiponectin promoter may have functional PPARgamma-response elements. Several observations showed that the adiponectin and aP2 genes can be differentially regulated in adipocytes: (1) Topiramate, an anti-epileptic agent with weight-reducing properties, increased adiponectin mRNA levels and secretion, but did not, like the thiazolidinediones, increase aP2 expression; (2) IL-6 reduced adiponectin, but significantly increased, aP2 expression; and (3) TNFalpha inhibited adiponectin, but paradoxically increased, aP2 expression in PPARgamma2-infected C/EBPalpha null cells. These data show that activation of the adiponectin gene can be separated from effects on adipogenic genes. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:933 / 939
页数:7
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