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综述:过氧化物酶体增殖物激活受体 γ 作为肥胖物的作用靶点。

Minireview: PPARγ as the target of obesogens.

机构信息

Department of Developmental and Cell Biology, University of California, Irvine, CA 92697-2300, United States.

出版信息

J Steroid Biochem Mol Biol. 2011 Oct;127(1-2):4-8. doi: 10.1016/j.jsbmb.2011.01.005. Epub 2011 Jan 18.

Abstract

The peroxisome proliferator-activated receptor gamma (PPARγ) is a key regulator of adipogenesis and is medically important for its connections to obesity and the treatment of type II diabetes. Activation of this receptor by certain natural or xenobiotic compounds has been shown to stimulate adipogenesis in vitro and in vivo. Obesogens are chemicals that ultimately increase obesity through a variety of potential mechanisms, including activation of PPARγ. The first obesogen for which a definitive mechanism of action has been elucidated is the PPARγ and RXR activator tributyltin; however, not all chemicals that activate PPARγ are adipogenic or correlated with obesity in humans. There are multiple mechanisms through which obesogens can target PPARγ that may not involve direct activation of the receptor. Ligand-independent mechanisms could act through obesogen-mediated post-translational modification of PPARγ which cause receptor de-repression or activation. PPARγ is active in multipotent stem cells committing to the adipocyte fate during fat cell development. By modifying chromatin structure early in development, obesogens have the opportunity to influence the promoter activity of PPARγ, or the ability of PPARγ to bind to its target genes, ultimately biasing the progenitor pool towards the fat lineage. Obesogens that act by directly or indirectly activating PPARγ, by increasing the levels of PPARγ protein, or enhancing its recruitment to promoters of key genes in the adipogenic pathway may ultimately play an important role in adipogenesis and obesity.

摘要

过氧化物酶体增殖物激活受体 γ(PPARγ)是脂肪生成的关键调节剂,与肥胖和 II 型糖尿病的治疗密切相关。某些天然或外源性化合物激活该受体已被证明可在体外和体内刺激脂肪生成。肥胖物是通过多种潜在机制最终导致肥胖的化学物质,包括激活 PPARγ。第一个明确作用机制的肥胖物是 PPARγ 和 RXR 激活剂三丁基锡;然而,并非所有激活 PPARγ 的化学物质都是致肥胖的,或与人类肥胖相关。肥胖物可以通过多种可能不涉及受体直接激活的机制靶向 PPARγ。配体非依赖性机制可能通过肥胖物介导的 PPARγ 翻译后修饰起作用,导致受体去抑制或激活。PPARγ 在脂肪细胞发育过程中多能干细胞向脂肪细胞命运分化时是活跃的。通过在早期发育过程中修饰染色质结构,肥胖物有机会影响 PPARγ 的启动子活性,或影响 PPARγ 与其靶基因结合的能力,最终使祖细胞库偏向脂肪谱系。通过直接或间接激活 PPARγ、增加 PPARγ 蛋白水平或增强其募集到脂肪生成途径关键基因启动子的肥胖物,可能最终在脂肪生成和肥胖中发挥重要作用。

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