Linebaugh B E, Rillema J A
Endocrinology. 1979 Sep;105(3):806-11. doi: 10.1210/endo-105-3-806.
Monolayer cultures of mammary gland epithelial cells were prepared from the abdominal glands of midpregnancy mice. After collagenase digestion of mammary tissue and separation by differential centrifugation, the isolated epithelial cells were cultured in Eagle's Minimal Essential Medium supplemented with 10% fetal bovine serum and insulin (6 micrograms/ml). Six days later, when the cultures were in log growth and nearly confluent, the effects of insulin and/or hydrocortisone on the rates of RNA, DNA, and protein synthesis were determined in a serum-free medium. At physiological concentrations, insulin enhanced the rates of uptake and incorporation of [3H]uridine into RNA, of [3H]thymidine into DNA, and of [3H]leucine into protein. Hydrocortisone was shown to be biphasic with regard to concentration in attenuating or augmenting insulin's effects on macromolecular synthesis.
从妊娠中期小鼠的腹部腺体制备乳腺上皮细胞单层培养物。在用胶原酶消化乳腺组织并通过差速离心分离后,将分离的上皮细胞培养在补充有10%胎牛血清和胰岛素(6微克/毫升)的伊格尔最低限度基本培养基中。六天后,当培养物处于对数生长期且几乎汇合时,在无血清培养基中测定胰岛素和/或氢化可的松对RNA、DNA和蛋白质合成速率的影响。在生理浓度下,胰岛素提高了[3H]尿苷掺入RNA、[3H]胸苷掺入DNA以及[3H]亮氨酸掺入蛋白质的摄取和掺入速率。氢化可的松在减弱或增强胰岛素对大分子合成的影响方面表现出浓度双相性。