血管生成和可塑性:促红细胞生成素在血管系统中的作用。

Zhao Zhong Chong, Jing-Qiong Kang, Kenneth Maiese
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引用次数: 123

摘要

促红细胞生成素(EPO)的主要功能之一是刺激红细胞前体的成熟。然而,EPO最近被证明可以调节多能干细胞中的一系列细胞信号转导通路,以执行除红细胞生成之外的多种功能。促生成素的产生受到缺氧和缺氧诱导因子的密切调节。EPO一旦产生,就成为调节内皮细胞增殖和迁移、红细胞生成和血管抵抗的强大刺激物。在信号转导级联的下游,EPO参与多种细胞途径,例如涉及Janus激酶2、信号转导和转录激活因子(STATs)、丝裂原活化蛋白激酶(MAPKs)、Bcl-x(L)、蛋白激酶B、蛋白激酶C和半胱氨酸蛋白酶的细胞途径,通过高度保守的机制为血管系统提供“可塑性”。EPO最近也被证明通过两种不同的成分来抑制细胞凋亡的诱导,这两种成分涉及维持基因组DNA的完整性和保存细胞膜的不对称性。认识到血管系统中EPO的多电位属性可能会进一步发展治疗策略,以延缓退行性疾病的发作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiogenesis and plasticity: role of erythropoietin in vascular systems.

One of the principal functions of erythropoietin (EPO) is to stimulate the maturation of erythroid precursors. Yet EPO has recently been shown to modulate a host of cellular signal transduction pathways in pluripotent stem cells to perform multiple functions other than erythropoiesis. The production of EPO is tightly modulated by the loss of oxygen and the hypoxia-inducible factor 1. Once generated, EPO becomes a robust stimulus which regulates endothelial cell proliferation and migration as well as erythropoiesis and vascular resistance. Further downstream in the signal transduction cascade, EPO engages diverse cellular pathways--such as those involving Janus kinase 2, signal transducers and activators of transcription (STATs), mitogen-activated protein kinases (MAPKs), Bcl-x(L), protein kinase B, protein kinase C, and cysteine proteases--to provide "plasticity" to vascular systems through highly conserved mechanisms. EPO also has recently been demonstrated to inhibit the induction of apoptosis through two distinct components that involve the maintenance of the integrity of genomic DNA and the preservation of cellular membrane asymmetry. Recognition of the multipotential attributes of EPO for vascular systems may further the progress of the development of therapeutic strategies to delay the onset of degenerative diseases.

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