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过氧化物酶体增殖物激活受体δ(PPARδ)介导的前脂肪细胞增殖和基因表达调控依赖于环磷酸腺苷(cAMP)信号传导。

Peroxisome proliferator-activated receptor delta (PPARdelta )-mediated regulation of preadipocyte proliferation and gene expression is dependent on cAMP signaling.

作者信息

Hansen J B, Zhang H, Rasmussen T H, Petersen R K, Flindt E N, Kristiansen K

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense University, DK-5230 Odense M, Denmark.

出版信息

J Biol Chem. 2001 Feb 2;276(5):3175-82. doi: 10.1074/jbc.M005567200. Epub 2000 Nov 7.

Abstract

The peroxisome proliferator-activated receptor gamma (PPARgamma) is a key regulator of terminal adipocyte differentiation. PPARdelta is expressed in preadipocytes, but the importance of this PPAR subtype in adipogenesis has been a matter of debate. Here we present a critical evaluation of the role of PPARdelta in adipocyte differentiation. We demonstrate that treatment of NIH-3T3 fibroblasts overexpressing PPARdelta with standard adipogenic inducers led to induction of PPARgamma2 expression and terminal adipocyte differentiation in a manner that was strictly dependent on simultaneous administration of a PPARdelta ligand and methylisobutylxanthine (MIX) or other cAMP elevating agents. We further show that ligands and MIX synergistically stimulated PPARdelta-mediated transactivation. In 3T3-L1 preadipocytes, simultaneous administration of a PPARdelta-selective ligand and MIX significantly enhanced the early expression of PPARgamma and ALBP/aP2, but only modestly promoted terminal differentiation as determined by lipid accumulation. Finally, we provide evidence that synergistic activation of PPARdelta promotes mitotic clonal expansion in 3T3-L1 cells with or without forced expression of PPARdelta. In conclusion, our results suggest that PPARdelta may play a role in the proliferation of adipocyte precursor cells, whereas activation of endogenous PPARdelta in 3T3-L1 cells appears to have only minor impact on the processes leading to terminal adipocyte differentiation.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)是终末脂肪细胞分化的关键调节因子。PPARδ在前脂肪细胞中表达,但其在脂肪生成中的重要性一直存在争议。在此,我们对PPARδ在脂肪细胞分化中的作用进行了批判性评估。我们证明,用标准脂肪生成诱导剂处理过表达PPARδ的NIH-3T3成纤维细胞,会以严格依赖于同时给予PPARδ配体和甲基异丁基黄嘌呤(MIX)或其他cAMP升高剂的方式诱导PPARγ2表达和终末脂肪细胞分化。我们进一步表明,配体和MIX协同刺激PPARδ介导的反式激活。在3T3-L1前脂肪细胞中,同时给予PPARδ选择性配体和MIX可显著增强PPARγ和ALBP/aP2的早期表达,但通过脂质积累测定,仅适度促进终末分化。最后,我们提供证据表明,PPARδ的协同激活在有或没有强制表达PPARδ的3T3-L1细胞中促进有丝分裂克隆扩增。总之,我们的结果表明,PPARδ可能在脂肪细胞前体细胞的增殖中起作用,而在3T3-L1细胞中内源性PPARδ的激活似乎对导致终末脂肪细胞分化的过程只有轻微影响。

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