Sasaki T, Enami J
Research Laboratory, Zenyaku Kogyo Co., Ltd., Tokyo, Japan.
Zoolog Sci. 1996 Aug;13(4):587-91. doi: 10.2108/zsj.13.587.
Mammary epithelial cells isolated from pregnant mice were plated on a collagen gel matrix and cultured in a serum-free medium supplemented with combinations of insulin, dexamethasone and prolactin (PRL). After the cells formed a monolayer, the collagen gel was detached from the culture dish and allowed to float in the medium. Quantification of gamma-casein mRNA by a competitive PCR method revealed that the cells on the floating gel accumulated considerably larger amounts of gamma-casein mRNA than the cells on the gel remained attached to the dish. Under these floating collagen gel culture conditions, addition of both dexamethasone and PRL to the insulin-supplemented basal medium maximally stimulated the accumulation of gamma-casein mRNA. These observations strongly suggest that the status of the extracellular matrix as well as hormones controls the differentiation of mouse mammary epithelial cells at the mRNA level.
从怀孕小鼠分离出的乳腺上皮细胞接种在胶原凝胶基质上,并在补充了胰岛素、地塞米松和催乳素(PRL)组合的无血清培养基中培养。细胞形成单层后,将胶原凝胶从培养皿中分离出来,使其在培养基中漂浮。通过竞争性PCR方法对γ-酪蛋白mRNA进行定量分析,结果显示,漂浮凝胶上的细胞积累的γ-酪蛋白mRNA量比仍附着在培养皿上的凝胶上的细胞多得多。在这些漂浮胶原凝胶培养条件下,向补充了胰岛素的基础培养基中添加地塞米松和PRL,可最大程度地刺激γ-酪蛋白mRNA的积累。这些观察结果有力地表明,细胞外基质的状态以及激素在mRNA水平上控制着小鼠乳腺上皮细胞的分化。