Buset M, Winawer S, Friedman E
In Vitro Cell Dev Biol. 1987 Jun;23(6):403-12. doi: 10.1007/BF02623855.
An improved method for the attachment and growth of normal human colonic epithelial cells from minute 1 to 3-mm3 biopsies has been developed. This yields four times as many cultured cells per biopsy than older methods, with a success rate of 97% in a series of 29 biopsies. Fetal bovine serum was eliminated from the medium, the medium pH was decreased to 6.7, the oxygen tension in the incubator was decreased to 3%, and the NCTC 168 medium was supplemented with ethanolamine, phosphoethanolamine, hydrocortisone, ascorbic acid, transferrin, glutamine, insulin, epidermal growth factor, pentagastrin, and deoxycholic acid. The best substrate for cell attachment was a mixture of ungelled collagen I and bovine serum albumin. This substrate was better than the identical mixture with fibronectin added, fibronectin alone, a thin gelatin film, collagen IV with or without fibronectin, and basement membrane preparations from four different cell lines.
已开发出一种改进方法,用于从1至3立方毫米的活检组织中附着和培养正常人结肠上皮细胞。与旧方法相比,每次活检培养出的细胞数量是原来的四倍,在一系列29次活检中成功率为97%。培养基中去除了胎牛血清,将培养基pH值降至6.7,将培养箱中的氧张力降至3%,并在NCTC 168培养基中添加了乙醇胺、磷酸乙醇胺、氢化可的松、抗坏血酸、转铁蛋白、谷氨酰胺、胰岛素、表皮生长因子、五肽胃泌素和脱氧胆酸。细胞附着的最佳底物是未凝胶化的I型胶原蛋白和牛血清白蛋白的混合物。这种底物比添加了纤连蛋白的相同混合物、单独的纤连蛋白、薄明胶膜、含或不含纤连蛋白的IV型胶原蛋白以及来自四种不同细胞系的基底膜制剂更好。