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PPAR7 signalling and vascular cells in 2003

机译:PPAR7 2003年的信号和血管细胞

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Peroxisome proliferator-activated receptor(gamma) (PPAR(gamma)) is a transcription factor belonging to the nuclear hormone receptor superfamily. PPAR(gamma) binds the insulin-sensitizing thiazolidinediones (TZDs) and is prominently upregulated in intimal vascular smooth muscle cells (VSMC) after mechanical injury to the vessel wall Several TZD PPAR(gamma) ligands have been shown to inhibit neointima formation.Suppression of intimal hyperplasia by PPAR7 ligands likely results from their activity to inhibit VSMC growth and to promote apoptosis. This review summarizes molecular pathways through which PPAR(gamma) regulates the expression and function of multiple cell cycle and apoptosis genes resulting in decreased VSMC proliferation and inhibition of neointima formation.
机译:过氧化物体增殖物激活受体(γ)(PPAR(γ))是属于核激素受体超家族的转录因子。 PPAR(γ)结合胰岛素敏化噻唑烷基二唑(TZDS),并且在血管壁的机械损伤后突出地上调在血管壁上的机械损伤几个TZD PPAR(γ)配体中被证明抑制新内膜形成。抑制PPAR7配体的内膜增生可能来自其活性的结果,以抑制VSMC的生长和促进细胞凋亡。本综述总结了PPAR(γ)调节多细胞周期和细胞凋亡基因的表达和功能的分子途径,导致VSMC增殖降低和内部地区的抑制。

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