Gustafson Birgit, Jack Maia M, Cushman Samuel W, Smith Ulf
Department of Internal Medicine, The Lundberg Laboratory for Diabetes Research, The Sahlgrenska Academy at Göteborg University, Göteborg SE-413 45, Sweden.
Biochem Biophys Res Commun. 2003 Sep 5;308(4):933-9. doi: 10.1016/s0006-291x(03)01518-3.
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.
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。