Elstow S F, Schor A M, Weiss J B
Invest Ophthalmol Vis Sci. 1985 Jan;26(1):74-9.
Two methods were used to extract angiogenic activity from bovine retina. Both methods initially gave rise to nondialyzable (greater than 10,000 Mr) fractions with angiogenic activity. However, after anion exchange chromatography, 20% of the extracts from one of the two methods (method 2) contained a small molecule with angiogenic activity (Mr 300-600). Alcohol treatment of high molecular mass fractions from both methods also released a low molecular mass angiogenic factor (Mr 300-600). No angiogenic activity was left in the nondialyzable residue. The high molecular mass angiogenic fraction obtained by method 1 after DEAE-cellulose chromatography contained a protein immunologically and electrophoretically identical to bovine serum albumin. The low molecular mass retinal angiogenic factor was able to stimulate microvessel endothelial cell proliferation as well as being positive in the chick chorioallantoic membrane test. The presence of a protein carrier system for a small angiogenesis factor is proposed. This would explain discrepancies in the apparent molecular mass of retinal angiogenic factors described previously.
采用两种方法从牛视网膜中提取血管生成活性物质。两种方法最初都产生了具有血管生成活性的不可透析部分(分子量大于10,000)。然而,经过阴离子交换色谱法后,两种方法之一(方法2)的提取物中有20%含有一种具有血管生成活性的小分子(分子量300 - 600)。用酒精处理两种方法得到的高分子量部分也释放出一种低分子量血管生成因子(分子量300 - 600)。不可透析的残渣中没有剩余血管生成活性。方法1在DEAE - 纤维素色谱法后得到的高分子量血管生成部分含有一种在免疫学和电泳方面与牛血清白蛋白相同的蛋白质。低分子量视网膜血管生成因子能够刺激微血管内皮细胞增殖,并且在鸡胚绒毛尿囊膜试验中呈阳性。有人提出存在一种针对小血管生成因子的蛋白质载体系统。这将解释先前描述的视网膜血管生成因子表观分子量的差异。