Department of Neurology Stroke Division, Center for Neural Development and Disease, and Interdepartmental Graduate Program in Neuroscience, University of Rochester School of Medicine & Dentistry, Rochester, New York 14642, USA.
Neuroscientist. 2009 Dec;15(6):579-88. doi: 10.1177/1073858409332405.
Astrocytes are increasingly recognized for their impact on neuronal function and viability in health and disease. Hypoxia has Janus-faced influences on astrocytes and their ability to support neuronal viability. For example, hypoxia induces astrocyte-dependent protection of neurons following hypoxia preconditioning. Yet, hypoxia induces processes in astrocytes that augment neuronal death in other situations, such as the coincidence of hypoxia with inflammatory signaling. A complex array of gene expression is induced by hypoxia within astrocytes and neurons through multiple transcription factors and intracellular molecular pathways. The hypoxia inducible factors (HIFs) are transcription factors that are likely instrumental in orchestrating adaptive and pathological functions of astrocytes. As such, the HIFs are postulated to mediate both adaptive and pathological functions during hypoxia/ ischemia. Identifying the conditions under which hypoxia induces signaling in astrocytes that alters autonomous or neuronal survival will undoubtedly have important implications regarding the development of new strategies for stroke treatment.
星形胶质细胞在健康和疾病状态下对神经元功能和存活的影响正越来越受到关注。缺氧对星形胶质细胞及其支持神经元存活的能力具有两面性的影响。例如,缺氧诱导星形胶质细胞依赖性的神经元缺氧预处理保护。然而,缺氧诱导星形胶质细胞中的某些过程会在其他情况下增加神经元死亡,例如缺氧与炎症信号同时发生。通过多种转录因子和细胞内分子途径,缺氧在星形胶质细胞和神经元中诱导出一系列复杂的基因表达。缺氧诱导因子(HIFs)是转录因子,可能在协调星形胶质细胞的适应性和病理性功能中起关键作用。因此,HIFs 被假设在缺氧/缺血期间介导适应性和病理性功能。确定缺氧诱导星形胶质细胞信号改变自主或神经元存活的条件无疑将对开发新的中风治疗策略具有重要意义。