Morris R J, Tacker K C, Baldwin J K, Fischer S M, Slaga T J
Cancer Lett. 1987 Mar;34(3):297-304. doi: 10.1016/0304-3835(87)90180-7.
A culture medium has been formulated to support the long-term proliferation and differentiation of normal murine epidermal cells in primary cultures. This formulation is based upon MCDB-151 modified by the addition of 1.2 mM Ca2+, 1% fetal bovine serum (FBS) or 0.1% purified bovine serum albumin (BSA), trace elements, and growth supplements. For 4-12 weeks, the cultures demonstrate desmosomes, keratin fibers, basal proliferation, and stratification characteristic of keratinocytes. The addition of 12-O-tetradecanoylphorbol-13-acetate (TPA) resulted in approximately 70% cellular detachment, but with continued treatment, the remaining cells proliferated to confluence and stratified. This culture medium has application to a number of studies related to skin carcinogenesis in the murine model system that have not previously been possible.
已配制一种培养基,以支持原代培养的正常小鼠表皮细胞长期增殖和分化。该配方基于MCDB - 151,并添加了1.2 mM钙离子、1%胎牛血清(FBS)或0.1%纯化牛血清白蛋白(BSA)、微量元素和生长补充剂。在4至12周内,培养物表现出桥粒、角蛋白纤维、基底增殖以及角质形成细胞特有的分层现象。添加12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)导致约70%的细胞脱离,但持续处理后,剩余细胞增殖至汇合并分层。这种培养基可应用于小鼠模型系统中许多以前无法进行的与皮肤癌发生相关的研究。