Muñoz-Chápuli R, Quesada A R, Angel Medina M
Department of Animal Biology, Faculty of Science, University of Málaga, 29071, Málaga, Spain.
Cell Mol Life Sci. 2004 Sep;61(17):2224-43. doi: 10.1007/s00018-004-4070-7.
Endothelial cells receive multiple information from their environment that eventually leads them to progress along all the stages of the process of formation of new vessels. Angiogenic signals promote endothelial cell proliferation, increased resistance to apoptosis, changes in proteolytic balance, cytoskeletal reorganization, migration and, finally, differentiation and formation of a new vascular lumen. We aim to review herein the main signaling cascades that become activated in angiogenic endothelial cells as well as the opportunities of modulating angiogenesis through pharmacological interference with these signaling mechanisms. We will deal mainly with the mitogen-activated protein kinases pathway, which is very important in the transduction of proliferation signals; the phosphatidylinositol-3-kinase/protein kinase B signaling system, particularly essential for the survival of the angiogenic endothelium; the small GTPases involved in cytoskeletal reorganization and migration; and the kinases associated to focal adhesions which contribute to integrate the pathways from the two main sources of angiogenic signals, i.e. growth factors and the extracellular matrix.
内皮细胞从其周围环境接收多种信息,这些信息最终引导它们经历新血管形成过程的所有阶段。血管生成信号促进内皮细胞增殖、增强对细胞凋亡的抵抗、改变蛋白水解平衡、细胞骨架重组、迁移,最终实现分化并形成新的血管腔。我们旨在在此综述在血管生成内皮细胞中被激活的主要信号级联反应,以及通过对这些信号机制进行药理学干预来调节血管生成的机会。我们将主要讨论丝裂原活化蛋白激酶途径,其在增殖信号转导中非常重要;磷脂酰肌醇-3-激酶/蛋白激酶B信号系统,对血管生成内皮细胞的存活尤为关键;参与细胞骨架重组和迁移的小GTP酶;以及与粘着斑相关的激酶,这些激酶有助于整合来自血管生成信号的两个主要来源即生长因子和细胞外基质的信号通路。