Hubbi Maimon E, Semenza Gregg L
Department of Internal Medicine, Division of Cardiology, The University of Texas Southwestern Medical Center, Dallas, Texas; and.
Departments of Pediatrics, Medicine, Oncology, Radiation Oncology and Biological Chemistry; Vascular Program, Institute for Cell Engineering; and McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland
Am J Physiol Cell Physiol. 2015 Dec 15;309(12):C775-82. doi: 10.1152/ajpcell.00279.2015. Epub 2015 Oct 21.
Hypoxia is a physiological cue that impacts diverse physiological processes, including energy metabolism, autophagy, cell motility, angiogenesis, and erythropoiesis. One of the key cell-autonomous effects of hypoxia is as a modulator of cell proliferation. For most cell types, hypoxia induces decreased cell proliferation, since an increased number of cells, with a consequent increase in O2 demand, would only exacerbate hypoxic stress. However, certain cell populations maintain cell proliferation in the face of hypoxia. This is a common pathological hallmark of cancers, but can also serve a physiological function, as in the maintenance of stem cell populations that reside in a hypoxic niche. This review will discuss major molecular mechanisms by which hypoxia regulates cell proliferation in different cell populations, with a particular focus on the role of hypoxia-inducible factors.
缺氧是一种影响多种生理过程的生理信号,这些生理过程包括能量代谢、自噬、细胞运动、血管生成和红细胞生成。缺氧对细胞自主产生的关键作用之一是作为细胞增殖的调节因子。对于大多数细胞类型而言,缺氧会导致细胞增殖减少,因为细胞数量增加会随之增加对氧气的需求,这只会加剧缺氧应激。然而,某些细胞群体在缺氧情况下仍能维持细胞增殖。这是癌症常见的病理特征,但也可发挥生理功能,比如维持处于缺氧微环境中的干细胞群体。本综述将讨论缺氧调节不同细胞群体中细胞增殖的主要分子机制,尤其关注缺氧诱导因子的作用。