Distler J H W, Hirth A, Kurowska-Stolarska M, Gay R E, Gay S, Distler O
WHO Collaborating Center for Molecular Biology and Novel Therapeutic Strategies for Rheumatic Diseases, University Hospital, Zurich, Switzerland.
Q J Nucl Med. 2003 Sep;47(3):149-61.
The vascular system that ensures an adequate blood flow is required to provide the cells with sufficient supply of nutrients and oxygen. Two different mechanisms of the formation of new vessels can be distinguished: vasculogenesis, the formation of the first primitive vascular plexus de novo and angiogenesis, the formation of new vessels from preexisting ones. Both processes are regulated by a delicate balance of pro- and anti-angiogenic factors. Physiologically, angiostatic mediators outweigh the angiogenic molecules and angiogenesis does not occur. Under certain conditions such as tumor formation or wound healing, the positive regulators of angiogenesis predominate and the endothelium becomes activated. Angiogenesis is initiated by vasodilatation and an increased permeability. After destabilization of the vessel wall, endothelial cells proliferate, migrate and form a tube, which is finally stabilized by pericytes and smooth muscle cells. Numerous soluble growth factors and inhibitors, cytokines and proteases as well as extracellular matrix proteins and adhesion molecules strictly control this multi-step process. The properties and interactions of angiogenic molecules such as VEGFs, FGFs, angiopoietins, PDGF, angiogenin, angiotropin, HGF, CXC chemokines with ELR motif, PECAM-1, integrins and VE-cadherin as well as angiostatic key players such as angiostatin, endostatin, thrombospondin, CXC chemokines without ELR motif, PEDF are discussed in this review with respect to their molecular impact on angiogenesis.
确保充足血流的血管系统对于为细胞提供足够的营养和氧气供应是必需的。可以区分两种不同的新血管形成机制:血管生成,即从头形成第一个原始血管丛;以及血管生成,即从预先存在的血管形成新血管。这两个过程都受到促血管生成和抗血管生成因子微妙平衡的调节。在生理情况下,血管生成抑制介质超过血管生成分子,血管生成不会发生。在某些条件下,如肿瘤形成或伤口愈合,血管生成的正调节因子占主导,内皮细胞被激活。血管生成由血管舒张和通透性增加引发。血管壁不稳定后,内皮细胞增殖、迁移并形成管道,最终由周细胞和平滑肌细胞使其稳定。众多可溶性生长因子和抑制剂、细胞因子和蛋白酶以及细胞外基质蛋白和黏附分子严格控制这一多步骤过程。本综述讨论了血管生成分子如血管内皮生长因子(VEGFs)、成纤维细胞生长因子(FGFs)、血管生成素、血小板衍生生长因子(PDGF)、血管生成素、血管趋化素、肝细胞生长因子(HGF)、具有ELR基序的CXC趋化因子、血小板内皮细胞黏附分子-1(PECAM-1)、整合素和血管内皮钙黏蛋白,以及血管生成抑制关键因子如血管抑素、内皮抑素、血小板反应蛋白、不具有ELR基序的CXC趋化因子、色素上皮衍生因子(PEDF)对血管生成的分子影响。