Haslam S Z, Levely M L
Endocrinology. 1985 May;116(5):1835-44. doi: 10.1210/endo-116-5-1835.
Estrogens enhance proliferation of normal mouse mammary cells in vivo. However, when cultured alone, normal mouse mammary epithelial cells fail to exhibit a proliferative response to estrogen in vitro; the basis for this lack of in vitro responsiveness to estrogen is not known. The purpose of the present study is to determine if cultured normal mouse mammary cells possess estrogen receptors (ER) and/or progesterone receptors (PgR) and if the ER mechanism is functional, as measured by the ability of estrogens to regulate PgR. Recent findings that mammary fibroblasts can influence the behavior of mammary epithelial cells in vitro led us to investigate their effect on epithelial cell responsiveness to estrogen. In these studies, collagenase-dissociated mammary glands of midpregnant BALB/c mice were the source of mixed cultures (containing both epithelial cells and fibroblasts) and epithelial or fibroblast cultures. The purity of epithelial or fibroblast cultures was quantified immunocytochemically using antivimentin antibody as a fibroblast marker. Steroid hormone binding was quantified in intact cultured cells using [3H]R5020 and 17 beta-[3H]estradiol as the ligands. Specific high affinity binding sites for estrogen (Kd = 3.1 +/- 0.8 X 10(-10] and progestins (Kd = 3.3 +/- 1.2 X 10(-9) M) were detected in mixed cultures. To assess the possible role of mammary fibroblasts, we investigated cultures containing only fibroblasts which were derived by differential centrifugation. When 17 beta-estradiol was added to the culture medium, a significant (P less than 0.01) increase in PgR concentration was observed in mixed cultures. While mixed cultures maintain responsiveness to estrogen in vitro, as measured herein, the epithelial cultures, derived by differential centrifugation and Percoll gradient sedimentation, did not. However, estrogenic regulation of PgR appears to be specific to epithelial cells in mixed cultures, since fibroblast cultures neither contained PgR nor displayed estrogen-inducible PgR. The lack of responsiveness of epithelial cultures is not due to a loss or decrease in the ER concentration. Thus, the presence of mammary fibroblasts appears to be associated with epithelial cell responsiveness to estrogen in vitro.
雌激素可增强正常小鼠乳腺细胞在体内的增殖。然而,单独培养时,正常小鼠乳腺上皮细胞在体外对雌激素无增殖反应;这种体外对雌激素缺乏反应性的原因尚不清楚。本研究的目的是确定培养的正常小鼠乳腺细胞是否具有雌激素受体(ER)和/或孕激素受体(PgR),以及ER机制是否具有功能,通过雌激素调节PgR的能力来衡量。最近的研究发现乳腺成纤维细胞可在体外影响乳腺上皮细胞的行为,这促使我们研究它们对上皮细胞雌激素反应性的影响。在这些研究中,用胶原酶解离的妊娠中期BALB/c小鼠乳腺是混合培养物(包含上皮细胞和成纤维细胞)以及上皮或成纤维细胞培养物的来源。使用抗波形蛋白抗体作为成纤维细胞标志物,通过免疫细胞化学法定量上皮或成纤维细胞培养物的纯度。使用[3H]R5020和17β-[3H]雌二醇作为配体,在完整的培养细胞中定量类固醇激素结合。在混合培养物中检测到雌激素(Kd = 3.1 +/- 0.8 X 10(-10))和孕激素(Kd = 3.3 +/- 1.2 X 10(-9)M)的特异性高亲和力结合位点。为了评估乳腺成纤维细胞可能的作用,我们研究了通过差速离心获得的仅含成纤维细胞的培养物。当向培养基中添加17β-雌二醇时,在混合培养物中观察到PgR浓度显著(P小于0.01)增加。如本文所测,虽然混合培养物在体外保持对雌激素的反应性,但通过差速离心和Percoll梯度沉降获得的上皮培养物则不然。然而,PgR的雌激素调节似乎对混合培养物中的上皮细胞具有特异性,因为成纤维细胞培养物既不含有PgR也不显示雌激素诱导的PgR。上皮培养物缺乏反应性并非由于ER浓度的丧失或降低。因此,乳腺成纤维细胞的存在似乎与体外上皮细胞对雌激素的反应性相关。