血管生成过程中内皮细胞存活和凋亡的调控

E. Chavakis, S. Dimmeler
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引用次数: 264

摘要

血管生成过程在许多生理和病理条件中起着重要作用。抑制内皮细胞(EC)凋亡提供EC存活被认为是血管生成过程中的重要机制。许多血管生成生长因子抑制EC细胞凋亡。此外,内皮细胞与细胞外基质或细胞间的粘附促进了内皮细胞的存活。相反,越来越多的证据表明,诱导EC细胞凋亡可能会抑制血管生成。在这篇综述中,我们将重点关注血管生成过程中EC存活和凋亡的调控,特别是血管生成生长因子、内源性血管生成抑制剂(如血管抑制素、内皮抑制素和血小板反应蛋白-1)以及与细胞外基质的粘附对细胞内信号传导的影响和促进。此外,我们还讨论了粘附分子与生长因子之间的串扰效应。了解内皮细胞存活和凋亡调控的分子机制可能为开发新的治疗方法提供新的靶点,以促进组织缺血(如心肌新生血管)的血管生成或抑制新生血管依赖疾病(如肿瘤、糖尿病视网膜病变)的血管生成。
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Regulation of Endothelial Cell Survival and Apoptosis During Angiogenesis
The process of angiogenesis plays an important role in many physiological and pathological conditions. Inhibition of endothelial cell (EC) apoptosis providing EC survival is thought to be an essential mechanism during angiogenesis. Many of the angiogenic growth factors inhibit EC apoptosis. In addition, the adhesion of ECs to the extracellular matrix or intercellular adhesion promotes EC survival. In contrast, increasing evidence suggests that the induction of EC apoptosis may counteract angiogenesis. In this review, we focus on the regulation of EC survival and apoptosis during angiogenesis and especially on the effects and intracellular signaling promoted by angiogenic growth factors, endogenous angiogenic inhibitors (such as angiostatin, endostatin, and thrombospondin-1), and the adhesion to the extracellular matrix. Furthermore, we discuss the effects of cross talk between adhesion molecules and growth factors. Understanding the molecular mechanisms involved in the regulation of EC survival and apoptosis may provide new targets for the development of new therapies to enhance angiogenesis in the case of tissue-ischemia (eg, the neovascularization of myocardium) or to inhibit angiogenesis in the case of neovascularization-dependent disease (eg, tumor, diabetic retinopathy).
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