Diabetes and Obesity Research Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Diabetes and Obesity Research Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia School of Mathematics and Statistics, The University of Sydney, Sydney, New South Wales, Australia School of Information Technologies, The University of Sydney, Sydney, New South Wales, Australia.
Mol Cell Biol. 2014 Oct 1;34(19):3607-17. doi: 10.1128/MCB.00583-14. Epub 2014 Jul 21.
While adipogenesis is controlled by a cascade of transcription factors, the global gene expression profiles in the early phase of adipogenesis are not well defined. Using microarray analysis of gene expression in 3T3-L1 cells, we have identified evidence for the activity of 2,568 genes during the early phase of adipocyte differentiation. One of these, the ISL1 gene, was of interest since its expression was markedly upregulated 1 h after initiation of differentiation, with a subsequent rapid decline. Overexpression of ISL1 at early times during adipocyte differentiation but not at later times was found to profoundly inhibit differentiation. This was accompanied by moderate downregulation of peroxisome proliferator-activated receptor γ (PPARγ) levels, substantial downregulation of PPARγ downstream genes, and downregulation of bone morphogenetic protein 4 (BMP4) levels in preadipocytes. Readdition of BMP4 overcame the inhibitory effect of ISL1 on the expression of PPARγ but not aP2, a gene downstream of PPARγ, and BMP4 also partially rescued ISL1 inhibition of adipogenesis, an effect which is additive with rosiglitazone. These results suggest that ISL1 is intimately involved in early regulation of adipogenesis, modulating PPARγ expression and activity via BMP4-dependent and -independent mechanisms. Our time course gene expression survey sets the stage for further studies to explore other early and immediate regulators.
虽然脂肪生成受一系列转录因子的控制,但脂肪生成早期的全基因表达谱尚未完全确定。通过对 3T3-L1 细胞基因表达的微阵列分析,我们已经鉴定出在脂肪细胞分化的早期阶段有 2568 个基因的活性证据。其中,ISL1 基因引起了我们的兴趣,因为它在分化开始后 1 小时表达明显上调,随后迅速下降。发现在脂肪细胞分化的早期而不是后期过度表达 ISL1 会严重抑制分化。这伴随着过氧化物酶体增殖物激活受体 γ(PPARγ)水平的适度下调、PPARγ下游基因的大量下调以及前脂肪细胞中骨形态发生蛋白 4(BMP4)水平的下调。在添加 BMP4 后,克服了 ISL1 对 PPARγ表达的抑制作用,但对 PPARγ下游的 aP2 基因没有影响,BMP4 也部分挽救了 ISL1 对脂肪生成的抑制作用,这种作用与罗格列酮具有相加作用。这些结果表明,ISL1 密切参与脂肪生成的早期调控,通过 BMP4 依赖和非依赖机制调节 PPARγ 的表达和活性。我们的时间过程基因表达调查为进一步研究探索其他早期和即时调节因子奠定了基础。