Tan Joanne T M, McLennan Susan V, Song William W, Lo Lisa W-Y, Bonner James G, Williams Paul F, Twigg Stephen M
Discipline of Medicine, University of Sydney, Sydney, NSW 2006, Australia.
Am J Physiol Cell Physiol. 2008 Sep;295(3):C740-51. doi: 10.1152/ajpcell.00333.2007. Epub 2008 Jul 2.
Adipocyte differentiation is a key process implicated in the pathogenesis of obesity and insulin resistance. Its regulation is triggered by a cascade of transcription factors, including the CCAAT/enhancer binding proteins (C/EBPs) and peroxisome proliferator-activated receptor-gamma (PPARgamma). Growth factors such as transforming growth factor-beta1 (TGF-beta1) are known to inhibit adipocyte differentiation in vitro, via the C/EBP pathway, and in vivo, but whether a downstream mediator of TGF-beta1, connective tissue growth factor (CTGF), also known as CCN2, has a similar role is unknown. Mouse 3T3-L1 cells were differentiated into adipocytes by using standard methods, and effects and regulation of CTGF were studied. Intervention with recombinant human CTGF during differing stages of differentiation caused an inhibition in the development of the adipocyte phenotype, according to the gene expression of the differentiation markers adiponectin and PPARgamma, as well as suppression of lipid accumulation and expression of the lipogenic enzyme glycerol-3-phosphate dehydrogenase. Whereas CTGF gene expression promptly fell by 90% as 3T3-L1 preadipocytes differentiated into mature adipocytes, CTGF mRNA expression was induced by added TGF-beta1. CTGF applied to cells early in the course of differentiation inhibited total cell protein levels and nuclear localization of the beta-isoform of C/EBP (C/EBP-beta) and, subsequently, total cell C/EBP-alpha levels. CTGF also inhibited the adipocyte differentiation program in primary cultures of mouse preadipocytes. Expression of CTGF mRNA was twofold higher in the central fat depots of mice compared with subcutaneous fat, suggesting a potential role for CTGF in vivo. In summary, these data show that CTGF inhibits the adipocyte differentiation program.
脂肪细胞分化是肥胖症和胰岛素抵抗发病机制中的一个关键过程。其调控由一系列转录因子触发,包括CCAAT/增强子结合蛋白(C/EBP)和过氧化物酶体增殖物激活受体γ(PPARγ)。已知诸如转化生长因子β1(TGF-β1)等生长因子在体外通过C/EBP途径以及在体内抑制脂肪细胞分化,但TGF-β1的下游介质结缔组织生长因子(CTGF,也称为CCN2)是否具有类似作用尚不清楚。采用标准方法将小鼠3T3-L1细胞诱导分化为脂肪细胞,并研究CTGF的作用及调控机制。根据脂肪细胞分化标志物脂联素和PPARγ的基因表达,以及脂质积累的抑制和生脂酶甘油-3-磷酸脱氢酶的表达,在分化的不同阶段用重组人CTGF进行干预会抑制脂肪细胞表型的发育。随着3T3-L1前脂肪细胞分化为成熟脂肪细胞,CTGF基因表达迅速下降90%,而添加TGF-β1可诱导CTGF mRNA表达。在分化过程早期将CTGF应用于细胞会抑制总细胞蛋白水平以及C/EBPβ亚型(C/EBP-β)的核定位,随后抑制总细胞C/EBPα水平。CTGF还抑制小鼠前脂肪细胞原代培养中的脂肪细胞分化程序。与皮下脂肪相比,小鼠中央脂肪库中CTGF mRNA的表达高出两倍,这表明CTGF在体内具有潜在作用。总之,这些数据表明CTGF抑制脂肪细胞分化程序。