Davis H, Gascho C, Kiernan J A
In Vitro. 1976 Mar;12(3):192-7. doi: 10.1007/BF02796441.
Fragments of adult renal tissue were maintained as organ cultures for 7 days in HEPES-buffered medium 199, supplemented with 10% calf serum and antibiotics. Addition of aprotinin (10,000 kallikrein inhibitor units per ml) to the medium resulted in improved survival of the cells of the glomeruli and tubules and preserved the integrity of the glomerular, capsular and tubular basement membranes. Optimal results were obtained when aprotinin was present throughout the period of culturing. Inclusion of aprotinin in the medium for only the first 3 days in vitro slightly increased the numbers of surviving glomerular and tubular cells, but also promoted the growth of connective tissue in the explants and was detrimental to the basement membranes of the tubules. It is suggested that both the antiproteolytic and the carbohydrate-binding properties of aprotinin are involved in the mediation of the observed effects.
将成人肾组织碎片在添加了10%小牛血清和抗生素的HEPES缓冲培养基199中作为器官培养物维持7天。向培养基中添加抑肽酶(每毫升10,000激肽释放酶抑制单位)可提高肾小球和肾小管细胞的存活率,并保持肾小球、包膜和肾小管基底膜的完整性。当在整个培养期间都存在抑肽酶时可获得最佳结果。仅在体外培养的前3天将抑肽酶加入培养基中,可略微增加存活的肾小球和肾小管细胞数量,但也会促进外植体中结缔组织的生长,并且对肾小管基底膜有害。提示抑肽酶的抗蛋白水解特性和碳水化合物结合特性均参与了所观察到的效应的介导过程。