Kierszenbaum A L, Lea O, Petrusz P, French F S, Tres L L
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1675-9. doi: 10.1073/pnas.78.3.1675.
A method for the isolation and culture of epididymal epithelial cells obtained from pubertal and old adult rats is described. This method permits the establishment of primary cultures of these cells in monolayers from aggregates isolated from whole epididymides and major epididymal anatomical segments (caput, corpus, and cauda) after trypsin and collagenase digestions. A large number of cultured epididymal cells retain a differentiated function as demonstrated by the immunocytochemical and radioimmunoassay finding of acidic epididymal glycoprotein, a spermatozoa-coating protein secreted by the principal cells of rat epididymis. The proliferative potential of cultured epididymal cells obtained from pubertal and old adult donors can be documented by [3H]thymidine labeling and mitotic indices without significant loss of gene expression for acidic epididymal glycoprotein. Results of this study demonstrate that epididymal epithelial cells, consisting of a predominant population of principal cells, can be isolated, cultured, and maintained for up to 3 months.
本文描述了一种从青春期和成年老年大鼠获取附睾上皮细胞并进行分离培养的方法。该方法能够在胰蛋白酶和胶原酶消化后,从整个附睾以及附睾主要解剖段(头、体、尾)分离得到的细胞聚集体中,建立这些细胞的单层原代培养。免疫细胞化学和放射免疫分析发现,大鼠附睾主细胞分泌的精子包被蛋白——酸性附睾糖蛋白,大量培养的附睾细胞保留了分化功能。通过[³H]胸腺嘧啶核苷标记和有丝分裂指数可以证明,从青春期和成年老年供体获得的培养附睾细胞具有增殖潜力,且酸性附睾糖蛋白的基因表达没有明显损失。本研究结果表明,以主细胞为主的附睾上皮细胞可以分离、培养并维持长达3个月。