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Effect of PGC-1α on Proliferation, Migration, and Transdifferentiation of Rat Vascular Smooth Muscle Cells Induced by High Glucose

机译:PGC-1α对高糖诱导的大鼠血管平滑肌细胞增殖,迁移和转分化的影响

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摘要

We assessed the role of PGC-1α (PPARγ coactivator-1 alpha) in glucose-induced proliferation, migration, and inflammatory gene expression of vascular smooth muscle cells (VSMCs). We carried out phagocytosis studies to assess the role of PGC-1α in transdifferentiation of VSMCs by flow cytometry. We found that high glucose stimulated proliferation, migration and inflammatory gene expression of VSMCs, but overexpression of PGC-1α attenuated the effects of glucose. In addition, overexpression of PGC-1α decreased mRNA and protein level of VSMCs-related genes, and induced macrophage-related gene expression, as well as phagocytosis of VSMCs. Therefore, PGC-1α inhibited glucose-induced proliferation, migration and inflammatory gene expression of VSMCs, which are key features in the pathology of atherosclerosis. More importantly, PGC-1α transdifferentiated VSMCs to a macrophage-like state. Such transdifferentiation possibly increased the portion of VSMCs-derived foam cells in the plaque and favored plaque stability.
机译:我们评估了PGC-1α(PPARγcoactivator-1 alpha)在葡萄糖诱导的血管平滑肌细胞(VSMC)增殖,迁移和炎症基因表达中的作用。我们进行了吞噬作用研究,以通过流式细胞术评估PGC-1α在VSMCs分化中的作用。我们发现高葡萄糖刺激血管平滑肌细胞的增殖,迁移和炎性基因表达,但是PGC-1α的过表达减弱了葡萄糖的作用。另外,PGC-1α的过表达降低了VSMCs相关基因的mRNA和蛋白水平,并诱导了巨噬细胞相关基因的表达以及VSMC的吞噬作用。因此,PGC-1α抑制葡萄糖诱导的VSMC增殖,迁移和炎症基因表达,这是动脉粥样硬化病理的关键特征。更重要的是,PGC-1α将VSMC分化为巨噬细胞样状态。这种转分化可能会增加斑块中源自VSMC的泡沫细胞的比例,并有利于斑块的稳定性。

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