Hadley M A, Byers S W, Suárez-Quian C A, Kleinman H K, Dym M
J Cell Biol. 1985 Oct;101(4):1511-22. doi: 10.1083/jcb.101.4.1511.
Sertoli cell preparations isolated from 10-day-old rats were cultured on three different substrates: plastic, a matrix deposited by co-culture of Sertoli and peritubular myoid cells, and a reconstituted basement membrane gel from the EHS tumor. When grown on plastic, Sertoli cells formed a squamous monolayer that did not retain contaminating germ cells. Grown on the matrix deposited by Sertoli-myoid cell co-cultures, Sertoli cells were more cuboidal and supported some germ cells but did not allow them to differentiate. After 3 wk however, the Sertoli cells flattened to resemble those grown on plastic. In contrast, the Sertoli cells grown on top of the reconstituted basement membrane formed polarized monolayers virtually identical to Sertoli cells in vivo. They were columnar with an elaborate cytoskeleton. In addition, they had characteristic basally located tight junctions and maintained germ cells for at least 5 wk in the basal aspect of the monolayer. However, germ cells did not differentiate. Total protein, androgen binding protein, transferrin, and type I collagen secretion were markedly greater when Sertoli cells were grown on the extracellular matrices than when they were grown on plastic. When Sertoli cells were cultured within rather than on top of reconstituted basement membrane gels they reorganized into cords. After one week, tight junctional complexes formed between adjacent Sertoli cells, functionally compartmentalizing the cords into central (adluminal) and peripheral (basal) compartments. Germ cells within the cords continued to differentiate. Thus, Sertoli cells cultured on top of extracellular matrix components assume a phenotype and morphology more characteristic of the in vivo, differentiated cells. Growing Sertoli cells within reconstituted basement membrane gels induces a morphogenesis of the cells into cords, which closely resemble the organ from which the cells were dissociated and which provide an environment permissive for germ cell differentiation.
从10日龄大鼠分离得到的支持细胞制剂在三种不同的基质上培养:塑料、支持细胞与睾丸肌样细胞共培养沉积的基质以及EHS肿瘤的重组基底膜凝胶。当在塑料上生长时,支持细胞形成扁平的单层,不能保留污染的生殖细胞。在支持细胞 - 肌样细胞共培养沉积的基质上生长时,支持细胞更呈立方形,能支持一些生殖细胞,但不允许它们分化。然而,3周后,支持细胞变扁平,类似于在塑料上生长的细胞。相比之下,在重组基底膜上生长的支持细胞形成了与体内支持细胞几乎相同的极化单层。它们呈柱状,具有精细的细胞骨架。此外,它们具有特征性的位于基部的紧密连接,并在单层的基部维持生殖细胞至少5周。然而,生殖细胞没有分化。当支持细胞在细胞外基质上生长时,总蛋白、雄激素结合蛋白、转铁蛋白和I型胶原的分泌明显多于在塑料上生长时。当支持细胞在重组基底膜凝胶内部而非顶部培养时,它们会重新组织成索状。一周后,相邻支持细胞之间形成紧密连接复合体,将索状结构在功能上分隔为中央(近腔)和外周(基部)区室。索状结构内的生殖细胞继续分化。因此,在细胞外基质成分上培养的支持细胞呈现出更具体内分化细胞特征的表型和形态。在重组基底膜凝胶中培养支持细胞可诱导细胞形态发生形成索状结构,这与细胞解离所来自的器官非常相似,并提供了允许生殖细胞分化的环境。