Vasil'ev A V, Orekhov A N, Tertov V V, Kim K J, Tutel'ian V A
Vopr Med Khim. 1989 Jul-Aug;35(4):124-7.
Activity of lysosomal proteinases cathepsins A, B, C, D and L was studied in cultivated cells of human aorta intima, isolated from intact zone of aorta, from lipid stria and atherosclerotic patch. The highest enzymatic activity was detected in the lipid stria cells and the lowest activity - in atherosclerotic patch. Atherogenous blood serum, added simultaneously with pepstatin or leupeptine into the cell culture of intact aorta, caused a distinct increase in the proliferating activity of these cells and in the level of cholesterol accumulation, while activities of cathepsin D or B and L were inhibited by 80-100%, respectively. The data obtained suggest that lysosomal proteolytic system plays an important role in development of atheromatous impairment of vascular wall.
研究了溶酶体蛋白酶组织蛋白酶A、B、C、D和L在从主动脉完整区域、脂纹和动脉粥样硬化斑块分离的人主动脉内膜培养细胞中的活性。在脂纹细胞中检测到最高的酶活性,而在动脉粥样硬化斑块中活性最低。将致动脉粥样化血清与胃蛋白酶抑制剂或亮抑蛋白酶肽同时添加到完整主动脉的细胞培养物中,导致这些细胞的增殖活性和胆固醇积累水平明显增加,而组织蛋白酶D或B以及L的活性分别被抑制80% - 100%。获得的数据表明,溶酶体蛋白水解系统在血管壁动脉粥样硬化损伤的发展中起重要作用。