Kuettner K E, Pauli B U
Ciba Found Symp. 1983;100:163-73. doi: 10.1002/9780470720813.ch11.
Neovascularization of developing, repairing or neoplastic tissues is regulated, at least partially, by a family of proteins of low molecular mass (1000 less than mol mass less than 50 000 Da) which can be extracted from avascular tissues, such as hyaline cartilage, aorta or bladder epithelium, by mild salt solutions. These extractable proteins, functionally defined as anti-invasion factor (AIF), act as local regulators for some of the major mechanistic pathways by which endothelial cells are thought to invade tissues during neovascularization, mainly by matrix-degrading enzymes and by increased rates of migration and proliferation. AIF contains a spectrum of proteinase (collagenase) inhibitory activities, as well as an endothelial cell growth inhibitor. The endothelial cell growth inhibitor is directed against actively dividing endothelial cells in culture but has no effect on endothelial cell monolayers or any other cell lines tested. In tumours, the AIF-derived endothelial cell growth inhibitor may limit tumour growth to less than 2 mm in diameter by inhibiting tumour neovascularization.
发育、修复或肿瘤组织的血管生成至少部分受一组低分子量蛋白质(分子量1000 Da<分子量<50000 Da)的调节,这些蛋白质可通过温和盐溶液从无血管组织(如透明软骨、主动脉或膀胱上皮)中提取。这些可提取的蛋白质在功能上被定义为抗侵袭因子(AIF),作为一些主要机制途径的局部调节因子,在血管生成过程中,内皮细胞被认为主要通过基质降解酶以及增加迁移和增殖速率来侵入组织。AIF具有一系列蛋白酶(胶原酶)抑制活性以及一种内皮细胞生长抑制剂。内皮细胞生长抑制剂针对培养中活跃分裂的内皮细胞,但对内皮细胞单层或任何其他测试的细胞系均无作用。在肿瘤中,源自AIF的内皮细胞生长抑制剂可能通过抑制肿瘤血管生成将肿瘤生长限制在直径小于2毫米。