Hahm H A, Ip M M, Darcy K, Black J D, Shea W K, Forczek S, Yoshimura M, Oka T
Grace Cancer Drug Center, Roswell Park Memorial Institute, New York State Department of Health, Buffalo 14263.
In Vitro Cell Dev Biol. 1990 Aug;26(8):803-14. doi: 10.1007/BF02623622.
A serum-free primary culture system is described which allows normal rat mammary epithelial cells (RMECs) embedded within a reconstituted basement membrane to undergo extensive growth and functional differentiation as detected by synthesis and secretion of the milk products casein and lipid. RMECs isolated from mammary glands of immature virgin rats were seeded within an extracellular matrix preparation derived from the Engelbreth-Holm-Swarm sarcoma and cultured in a serum-free medium consisting of Dulbecco's modified Eagle's medium-F12 containing insulin, prolactin, progesterone, hydrocortisone, epidermal growth factor, bovine serum albumin, transferrin, and ascorbic acid. Casein synthesis and secretion were documented at the electron microscopic level as well as by an enzyme-linked immunosorbent assay (ELISA) assay using a polyclonal antibody against total rat caseins. Numerous secretory vesicles with casein micelles were noted near the apical surface of the RMECs, and secreted casein was observed in the lumen. These ultrastructural data were confirmed by the ELISA assay which showed that microgram amounts of casein per well were synthesized by the RMECs and that the amount of casein increased with time in culture. Using immunoblot analysis it was demonstrated that the full complement of casein proteins was synthesized. In addition to casein protein, beta-casein mRNA levels were shown to increase with time. Synthesized lipid was detected at both the light and electron microscopic levels. Phase contrast photomicrographs demonstrated extensive intracellular lipid accumulation within the ductal and lobuloalveolarlike colonies, and at the electron micrograph level, lipid droplets were predominantly localized near the apical surface of the RMECs. The lipid nature of these droplets was verified by oil red O staining. Results from this study demonstrate that RMECs from immature virgin rats proliferate extensively and rapidly develop the capacity to synthesize and secrete casein and lipid when grown within a reconstituted basement membrane under defined serum-free conditions. This unique system should thus serve as an excellent model in which the regulation of mammary development and gene expression can be investigated.
本文描述了一种无血清原代培养系统,该系统可使包埋于重组基底膜中的正常大鼠乳腺上皮细胞(RMECs)实现大量生长,并通过合成和分泌乳蛋白酪蛋白及脂质表现出功能分化。从未成熟处女大鼠乳腺分离的RMECs接种于源自Engelbreth-Holm-Swarm肉瘤的细胞外基质制剂中,并在一种无血清培养基中培养,该培养基由含有胰岛素、催乳素、孕酮、氢化可的松、表皮生长因子、牛血清白蛋白、转铁蛋白和抗坏血酸的杜氏改良 Eagle培养基-F12组成。酪蛋白的合成与分泌通过电子显微镜观察以及使用抗大鼠总酪蛋白的多克隆抗体进行的酶联免疫吸附测定(ELISA)得以记录。在RMECs顶表面附近观察到许多含有酪蛋白微胶粒的分泌小泡,且在管腔中观察到分泌的酪蛋白。这些超微结构数据通过ELISA测定得到证实,该测定表明RMECs每孔合成微克量的酪蛋白,且酪蛋白量随培养时间增加。通过免疫印迹分析证明合成了完整的酪蛋白蛋白。除了酪蛋白,β-酪蛋白mRNA水平也随时间增加。在光学和电子显微镜水平均检测到合成的脂质。相差显微镜照片显示在导管样和小叶腺泡样集落内有大量细胞内脂质积累,在电子显微镜水平,脂滴主要位于RMECs顶表面附近。这些脂滴的脂质性质通过油红O染色得以验证。本研究结果表明,在限定的无血清条件下,生长于重组基底膜内时,未成熟处女大鼠的RMECs可大量增殖,并迅速发展出合成和分泌酪蛋白及脂质的能力。因此,这个独特的系统应可作为研究乳腺发育和基因表达调控的优良模型。