Spicer Zachary, Millhorn David E
Department of Genome Sciences, University of Cincinnati Genome Research Institute, Cincinnati, OH 45237, USA.
Endocr Pathol. 2003 Winter;14(4):277-91. doi: 10.1385/ep:14:4:277.
A steady supply of oxygen is an absolute requirement for mammalian cells to maintain normal cellular functions. To answer the challenge that oxygen deprivation represents, mammals have evolved specialized cell types that can sense changes in oxygen tension and alter gene expression to enhance oxygen delivery to hypoxic areas. These oxygensensing cells are rare and difficult to study in vivo. As a result, pheochromocytoma (PC12) cells have become a vital in vitro model system for deciphering the molecular events that confer the hypoxia-resistant and oxygen-sensing phenotypes. Research over the last few years has revealed that the hypoxia response in PC12 cells involves the interactions of several signal transduction pathways (Ca2+/calmodulin-dependent kinases, Akt, SAPKs, and MAPKs) and transcription factors (HIFs, CREB, and c-fos/junB). This review summarizes the current understanding of the role these signal transduction pathways and transcription factors play in determining the hypoxic response.
持续供应氧气是哺乳动物细胞维持正常细胞功能的绝对必要条件。为应对缺氧带来的挑战,哺乳动物进化出了特殊的细胞类型,这些细胞能够感知氧张力的变化并改变基因表达,以增强向缺氧区域的氧气输送。这些氧感应细胞非常罕见,并且在体内很难进行研究。因此,嗜铬细胞瘤(PC12)细胞已成为一种至关重要的体外模型系统,用于解读赋予抗缺氧和氧感应表型的分子事件。过去几年的研究表明,PC12细胞中的缺氧反应涉及多种信号转导途径(钙/钙调蛋白依赖性激酶、Akt、应激激活蛋白激酶和丝裂原活化蛋白激酶)和转录因子(缺氧诱导因子、环磷腺苷效应元件结合蛋白以及c-原癌基因Fos/junB)之间的相互作用。本综述总结了目前对这些信号转导途径和转录因子在决定缺氧反应中所起作用的理解。