Strum J M, Hillman E A
In Vitro. 1981 Jan;17(1):33-43. doi: 10.1007/BF02618028.
Normal breast tissue from a 17-year-old girl was grown in organ culture for 3 weeks. A comparison was made between the effects on the epithelium of a defined culture medium containing various combinations of hormones and serum-supplemented medium that has been used to successfully maintain other human tissues for 4 months routinely, and in some cases for up to 1 year. After culture for 3 weeks the explants were exposed to [3H]thymidine and autoradiographs were prepared and evaluated in order to determine labeling indexes. The only serum-free defined medium that permitted any significant survival or labeling of the cells contained insulin + hydroxycortisone + prolactin. However, serum-supplemented medium along gave an even higher labeling index, and this was elevated more in media containing either progesterone or other combinations of hormones. Our study indicates that normal human breast (removed at the early postovulatory stage of the menstrual cycle) can be maintained in a differentiated state for 12 days in serum-supplemented media. By 2 weeks the cells had begun to migrate onto the surface of the explant. They then began to accumulate tonofilaments so that after 3 weeks in culture nearly all of the cells contained tonofilaments. The one exception was found in breast tissue cultured in the presence of human chorionic gonadotropin, where the cells maintained differentiated characteristics, despite the fact that they contained many lysosomes.
取自一名17岁女孩的正常乳腺组织在器官培养中生长了3周。对含有各种激素组合的特定培养基对上皮细胞的影响与血清补充培养基进行了比较,血清补充培养基已常规用于成功维持其他人体组织4个月,在某些情况下长达1年。培养3周后,将外植体暴露于[3H]胸腺嘧啶核苷,并制备和评估放射自显影片以确定标记指数。唯一允许细胞有任何显著存活或标记的无血清特定培养基含有胰岛素+氢化可的松+催乳素。然而,单独的血清补充培养基给出了更高的标记指数,并且在含有孕酮或其他激素组合的培养基中该指数升高得更多。我们的研究表明,正常人类乳腺(在月经周期排卵后期切除)在血清补充培养基中可以维持分化状态12天。到2周时,细胞开始迁移到外植体表面。然后它们开始积累张力丝,因此在培养3周后,几乎所有细胞都含有张力丝。唯一的例外是在人绒毛膜促性腺激素存在下培养的乳腺组织中发现的,尽管细胞含有许多溶酶体,但它们仍保持分化特征。