Suppr超能文献

ISL1 通过骨形态发生蛋白 4 依赖性和非依赖性机制调节过氧化物酶体增殖物激活受体 γ 的激活和早期脂肪生成。

ISL1 regulates peroxisome proliferator-activated receptor γ activation and early adipogenesis via bone morphogenetic protein 4-dependent and -independent mechanisms.

机构信息

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.

出版信息

Mol Cell Biol. 2014 Oct 1;34(19):3607-17. doi: 10.1128/MCB.00583-14. Epub 2014 Jul 21.

Abstract

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.

摘要

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。

相似文献

3
6-gingerol inhibits rosiglitazone-induced adipogenesis in 3T3-L1 adipocytes.
Phytother Res. 2014 Feb;28(2):187-92. doi: 10.1002/ptr.4976. Epub 2013 Mar 21.
5
Molecular mechanism of 1,25-dihydroxyvitamin D3 inhibition of adipogenesis in 3T3-L1 cells.
Am J Physiol Endocrinol Metab. 2006 May;290(5):E916-24. doi: 10.1152/ajpendo.00410.2005. Epub 2005 Dec 20.
7
Vanadium(IV)-chlorodipicolinate inhibits 3T3-L1 preadipocyte adipogenesis by activating LKB1/AMPK signaling pathway.
J Inorg Biochem. 2016 Sep;162:1-8. doi: 10.1016/j.jinorgbio.2016.06.013. Epub 2016 Jun 5.

引用本文的文献

2
Single cell full-length transcriptome of human subcutaneous adipose tissue reveals unique and heterogeneous cell populations.
iScience. 2022 Jul 16;25(8):104772. doi: 10.1016/j.isci.2022.104772. eCollection 2022 Aug 19.
4
Developmental programming: Adipose depot-specific transcriptional regulation by prenatal testosterone excess in a sheep model of PCOS.
Mol Cell Endocrinol. 2021 Mar 1;523:111137. doi: 10.1016/j.mce.2020.111137. Epub 2020 Dec 25.
7
ORTI: An Open-Access Repository of Transcriptional Interactions for Interrogating Mammalian Gene Expression Data.
PLoS One. 2016 Oct 10;11(10):e0164535. doi: 10.1371/journal.pone.0164535. eCollection 2016.
8
Control of adipocyte differentiation in different fat depots; implications for pathophysiology or therapy.
Front Endocrinol (Lausanne). 2015 Jan 30;6:1. doi: 10.3389/fendo.2015.00001. eCollection 2015.
9
A neuron-specific deletion of the microRNA-processing enzyme DICER induces severe but transient obesity in mice.
PLoS One. 2015 Jan 28;10(1):e0116760. doi: 10.1371/journal.pone.0116760. eCollection 2015.

本文引用的文献

1
What we talk about when we talk about fat.
Cell. 2014 Jan 16;156(1-2):20-44. doi: 10.1016/j.cell.2013.12.012.
2
Bmp4 expressed in preadipocytes is required for the onset of adipocyte differentiation.
Cytokine. 2013 Oct;64(1):138-45. doi: 10.1016/j.cyto.2013.07.011. Epub 2013 Aug 2.
3
Identification of the control region of pancreatic expression of Bmp4 in vitro and in vivo.
PLoS One. 2013 Apr 23;8(4):e61821. doi: 10.1371/journal.pone.0061821. Print 2013.
4
Adiposity and insulin resistance in humans: the role of the different tissue and cellular lipid depots.
Endocr Rev. 2013 Aug;34(4):463-500. doi: 10.1210/er.2012-1041. Epub 2013 Apr 2.
5
BMP4-mediated brown fat-like changes in white adipose tissue alter glucose and energy homeostasis.
Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):E798-807. doi: 10.1073/pnas.1215236110. Epub 2013 Feb 6.
6
WISP2 regulates preadipocyte commitment and PPARγ activation by BMP4.
Proc Natl Acad Sci U S A. 2013 Feb 12;110(7):2563-8. doi: 10.1073/pnas.1211255110. Epub 2013 Jan 28.
7
Adipogenesis: from stem cell to adipocyte.
Annu Rev Biochem. 2012;81:715-36. doi: 10.1146/annurev-biochem-052110-115718. Epub 2012 Mar 29.
8
Amplification and demultiplexing in insulin-regulated Akt protein kinase pathway in adipocytes.
J Biol Chem. 2012 Feb 24;287(9):6128-38. doi: 10.1074/jbc.M111.318238. Epub 2011 Dec 29.
9
Bone morphogenetic protein-3b (BMP-3b) is expressed in adipocytes and inhibits adipogenesis as a unique complex.
Int J Obes (Lond). 2012 May;36(5):725-34. doi: 10.1038/ijo.2011.124. Epub 2011 Jun 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验