首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC1α) is a metabolic regulator of intestinal epithelial cell fate
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Peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC1α) is a metabolic regulator of intestinal epithelial cell fate

机译:过氧化物酶体增殖物激活受体-γ共激活物1-α(PGC1α)是肠道上皮细胞命运的代谢调节剂

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摘要

Peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC1α) is a transcriptional coactivator able to up-regulate mitochondrial biogenesis, respiratory capacity, oxidative phosphorylation, and fatty acid β-oxidation with the final aim of providing a more efficient pathway for aerobic energy production. In the continuously renewed intestinal epithelium, proliferative cells in the crypts migrate along the villus axis and differentiate into mature enterocytes, increasing their respiratory capacity and finally undergoing apoptosis. Here we show that in the intestinal epithelial surface, PGC1α drives mitochondrial biogenesis and respiration in the presence of reduced antioxidant enzyme activities, thus determining the accumulation of reactive oxygen species and fostering the fate of enterocytes toward apoptosis. Combining gain- and loss-of-function genetic approaches in human cells and mouse models of intestinal cancer, we present an intriguing scenario whereby PGC1α regulates enterocyte cell fate and protects against tumorigenesis.
机译:过氧化物酶体增殖物激活受体-γ共激活因子1-α(PGC1α)是一种转录共激活因子,能够上调线粒体的生物发生,呼吸能力,氧化磷酸化和脂肪酸β-氧化,最终目的是为有氧运动提供更有效的途径能源生产。在不断更新的肠上皮中,隐窝中的增生细胞沿绒毛轴迁移并分化为成熟的肠上皮细胞,从而增加了它们的呼吸能力并最终经历了细胞凋亡。在这里我们表明,在肠上皮表面,PGC1α在抗氧化酶活性降低的情况下驱动线粒体的生物发生和呼吸作用,从而确定了活性氧的积累并促进了肠上皮细胞向凋亡的命运。结合人类细胞和小鼠小肠癌模型中功能获得和丧失功能的遗传方法,我们提出了一个有趣的场景,其中PGC1α调节肠上皮细胞的命运并防止肿瘤发生。

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