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将 αMSH 与 B16-F10 黑素瘤中的 PPARγ 连接。

Linking αMSH with PPARγ in B16-F10 melanoma.

机构信息

Laboratory of Cutaneous Physiopathology and Integrated Centre of Metabolomics Research, San Gallicano Dermatological Institute (IRCCS), Rome, Italy.

出版信息

Pigment Cell Melanoma Res. 2013 Jan;26(1):113-27. doi: 10.1111/j.1755-148X.2012.01042.x. Epub 2012 Sep 12.

Abstract

We have discovered a new α-melanocyte stimulating hormone (α-MSH)/peroxisome proliferator activated receptor-γ (PPAR-γ) connection in B16-F10 cells. Both PPAR-γ up-regulation and its induction as an active transcription factor were observed in response to α-MSH. The α-MSH/PPAR-γ connection influenced both pigmentation and proliferation. The forskolin-stimulated cAMP/PKA pathway was not able to induce either PPAR-γ translocation into the nucleus or PPAR-γ transcriptional activity. As the melanocortin-1 receptor, the specific receptor for the α-MSH, is a G-protein coupled receptor, we wondered whether the phosphatidylinositol [PI(4,5)P(2) /PLC(β) ] signal pathway was involved in mediating the α-MSH-dependent PPAR-γ activation. Employing inhibitors of PI(4,5)P(2) /PLC(β) pathway, the results of our experiments suggested that this pathway was promoted by α-MSH and that α-MSH played a role in mediating PPAR-γ activation. We have demonstrated, for the first time, that α-MSH induces the PI(4,5)P(2) /PLC(β) pathway, through analysis of the basic steps of the pathway. The α-MSH effect on PPAR-γ was independent of animal species and was not correlated with the physio-pathological status.

摘要

我们在 B16-F10 细胞中发现了一种新的 α-促黑素细胞激素(α-MSH)/过氧化物酶体增殖物激活受体-γ(PPAR-γ)联系。α-MSH 能上调 PPAR-γ,并使其作为活性转录因子诱导。α-MSH/PPAR-γ 的联系影响着色素沉着和增殖。福司可林刺激的 cAMP/PKA 途径不能诱导 PPAR-γ 转位入核或 PPAR-γ 转录活性。由于黑皮质素-1 受体是 α-MSH 的特异性受体,是 G 蛋白偶联受体,我们想知道磷脂酰肌醇 [PI(4,5)P(2)/PLC(β)]信号通路是否参与介导 α-MSH 依赖性 PPAR-γ 激活。通过使用 PI(4,5)P(2)/PLC(β)途径抑制剂,我们的实验结果表明该途径被 α-MSH 促进,并且 α-MSH 在介导 PPAR-γ 激活中起作用。我们首次通过分析该途径的基本步骤证明,α-MSH 通过诱导 PI(4,5)P(2)/PLC(β)途径来诱导 PPAR-γ 的激活。α-MSH 对 PPAR-γ 的影响与动物种类无关,也与生理病理状态无关。

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