Kirkland W L, Yang N S, Jorgensen T, Longley C, Furmanski P
J Natl Cancer Inst. 1979 Jul;63(1):29-41.
Normal and malignant human mammary epithelial cells were placed in culture. Normal cells were recovered from late-lactation milk and breast fluids, and malignant cells were isolated from primary breast tumors by collagenase digestion. The concentration of cells obtained from breast fluid samples was inversely proportional to the volume of fluid secreted. Most of these cells adhered rapidly to the substrate, did not replicate, displayed Fc receptor-dependent phagocytic activity, and were thus identified as macrophages. The remaining cells grew out into large islands comprised of one or two distinct morphologic types of mammary epithelial cells. Optimum growth of these cells was obtained in medium buffered to pH 6.8, and the epidermal growth factor markedly prolonged the exponential growth phase of the cells. Two morphologically distinct populations of epithelial cells were also observed in cultures established from individual breast tumors. Growth of the malignant cells was relatively unaffected by the pH of the culture medium, and the cells were unresponsive to exogenously added hormones. Overgrowth of malignant epithelial cells in primary cultures by stromal fibroblasts was retarded by replacement of standard growth medium with fresh medium containing a serum substitute; growth of the malignant epithelial cells was unaffected. A feeder layer of mitomycin C-treated human fibroblasts increased the plating efficiency of both normal and malignant cells in primary culture and also facilitated passage of these cells to secondary and tertiary cultures.
将正常和恶性人乳腺上皮细胞进行培养。正常细胞从哺乳后期的乳汁和乳腺液中获取,恶性细胞通过胶原酶消化从原发性乳腺肿瘤中分离得到。从乳腺液样本中获得的细胞浓度与分泌的液体体积成反比。这些细胞中的大多数迅速黏附于底物,不进行复制,表现出Fc受体依赖性吞噬活性,因此被鉴定为巨噬细胞。其余细胞生长成由一两种不同形态类型的乳腺上皮细胞组成的大岛状结构。这些细胞在pH值缓冲至6.8的培养基中生长最佳,表皮生长因子显著延长了细胞的指数生长期。在从单个乳腺肿瘤建立的培养物中也观察到两种形态不同的上皮细胞群体。恶性细胞的生长相对不受培养基pH值的影响,并且这些细胞对外源性添加的激素无反应。用含有血清替代品的新鲜培养基替换标准生长培养基可抑制原发性培养物中基质成纤维细胞对恶性上皮细胞的过度生长;恶性上皮细胞的生长不受影响。经丝裂霉素C处理的人成纤维细胞饲养层提高了原发性培养中正常和恶性细胞的接种效率,也促进了这些细胞传代至第二代和第三代培养。