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噻唑烷二酮类药物激活脂联素基因需要PPARγ2,但不需要C/EBPα——这是aP2基因和脂联素基因存在差异调控的证据。

Adiponectin gene activation by thiazolidinediones requires PPAR gamma 2, but not C/EBP alpha-evidence for differential regulation of the aP2 and adiponectin genes.

作者信息

Gustafson Birgit, Jack Maia M, Cushman Samuel W, Smith Ulf

机构信息

Department of Internal Medicine, The Lundberg Laboratory for Diabetes Research, The Sahlgrenska Academy at Göteborg University, Göteborg SE-413 45, Sweden.

出版信息

Biochem Biophys Res Commun. 2003 Sep 5;308(4):933-9. doi: 10.1016/s0006-291x(03)01518-3.

Abstract

We examined the role of PPAR gamma 2 and C/EBP alpha for adiponectin and aP2 gene activation in C/EBP alpha(-/-) fibroblasts by stably expressing PPAR gamma 2 or C/EBP alpha. PPAR gamma 2, but not PPAR gamma 1, mRNA markedly increased during the differentiation to adipocytes in cells expressing C/EBP alpha. 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/EBP alpha was present, suggesting that this transcription factor is important for full gene activation. Thiazolidinediones markedly activated the gene in PPAR gamma 2-expressing cells in the absence of C/EBP alpha, suggesting that the adiponectin promoter may have functional PPAR gamma-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 PPAR gamma 2-infected C/EBP alpha null cells. These data show that activation of the adiponectin gene can be separated from effects on adipogenic genes.

摘要

我们通过稳定表达过氧化物酶体增殖物激活受体γ2(PPARγ2)或CCAAT/增强子结合蛋白α(C/EBPα),研究了PPARγ2和C/EBPα在C/EBPα基因敲除成纤维细胞中对脂联素和脂肪细胞型脂肪酸结合蛋白2(aP2)基因激活的作用。在表达C/EBPα的细胞向脂肪细胞分化过程中,PPARγ2而非PPARγ1的信使核糖核酸(mRNA)显著增加。两种感染细胞系均分化为脂肪细胞表型,且aP2和脂联素的mRNA平行增加。然而,当存在C/EBPα时,脂联素mRNA水平显著更高,表明该转录因子对基因的完全激活很重要。噻唑烷二酮类药物在不存在C/EBPα的情况下能显著激活PPARγ2表达细胞中的该基因,提示脂联素启动子可能具有功能性PPARγ反应元件。多项观察结果表明,脂联素和aP2基因在脂肪细胞中可受到不同调控:(1)托吡酯是一种具有减肥特性的抗癫痫药物,可增加脂联素mRNA水平和分泌,但不像噻唑烷二酮类药物那样增加aP2表达;(2)白细胞介素6(IL-6)降低脂联素水平,但显著增加aP2表达;(3)肿瘤坏死因子α(TNFα)抑制脂联素,但在PPARγ2感染的C/EBPα基因敲除细胞中却反常地增加aP2表达。这些数据表明,脂联素基因的激活可与对脂肪生成基因的影响相分离。

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