Tung P S, Fritz I B
Dev Biol. 1987 Mar;120(1):139-53. doi: 10.1016/0012-1606(87)90112-6.
Addition of dibutyryl cyclic AMP (dbcAMP), methylisobutylxanthine (MIX), or cytochalasin D to co-cultures of Sertoli cells and testicular peritubular myoid cells blocks a series of morphogenetic changes which otherwise occur during culture. When Sertoli cells are plated directly onto preexisting layers of peritubular cells maintained under basal conditions, structures form which display many of the characteristics of germ cell-depleted seminiferous tubules. The presence of dbcAMP, MIX, or cytochalasin D, added at varying times after plating Sertoli cells, results in the inhibition of each successive stage of in vitro remodeling: the inhibition of migration of Sertoli cells, the inhibition of initial ridge formation, the blockage of subsequent formation of mounds and nodules of compacted Sertoli cell aggregates, the prevention of the formation of basal lamina and associated layers of extracellular matrix between Sertoli cell aggregates and surrounding peritubular cells, and the inhibition of tubule formation. The presence of dbcAMP also inhibits the migration of peritubular cells, contractions by these cells, and compaction of Sertoli cell aggregates. When intimate cell apposition is prevented by plating the two cell types on either side of a membrane filter, the morphogenetic cascade is blocked, and no formation of a germ cell-depleted seminiferous tubule-like structure occurs. Other effects of dbcAMP on cell shape, cell movement, and cell association patterns during co-culture are described. Possible mechanisms by which dbcAMP, MIX, or cytochalasin D blocks restructuring are discussed. Since each elicits perturbations of the cytoskeleton, we offer the interpretation that cytoskeletal changes may be correlated with the prevention of closely apposing cell compact and the inhibition of basement membrane formation. Interactions observed between Sertoli cells and peritubular cells during co-culture are postulated to be analogous to those occurring in other types of mesenchymal cell-epithelial cell interactions during organogenesis and during tubulogenesis in the fetal testis. Speculatively, the blockage by dbcAMP of the morphogenetic cascade in the co-cultured system may be related to the inhibition by dbcAMP of testis cord formation in organ cultures of fetal gonads reported by others.
向支持细胞与睾丸管周肌样细胞的共培养物中添加二丁酰环磷酸腺苷(dbcAMP)、甲基异丁基黄嘌呤(MIX)或细胞松弛素D,会阻断一系列在培养过程中原本会发生的形态发生变化。当将支持细胞直接接种到在基础条件下维持的预先存在的管周细胞层上时,会形成具有许多无生殖细胞生精小管特征的结构。在接种支持细胞后的不同时间添加dbcAMP、MIX或细胞松弛素D,会导致体外重塑的每个连续阶段受到抑制:抑制支持细胞的迁移、抑制初始嵴形成、阻断随后紧密排列的支持细胞聚集体形成丘和结节、防止在支持细胞聚集体与周围管周细胞之间形成基膜和细胞外基质相关层,以及抑制小管形成。dbcAMP的存在还会抑制管周细胞的迁移、这些细胞的收缩以及支持细胞聚集体的紧密排列。当通过将两种细胞类型接种在膜滤器的两侧来防止细胞紧密贴附时,形态发生级联反应被阻断,不会形成无生殖细胞生精小管样结构。还描述了dbcAMP在共培养过程中对细胞形状、细胞运动和细胞关联模式的其他影响。讨论了dbcAMP、MIX或细胞松弛素D阻断重组的可能机制。由于每种物质都会引发细胞骨架的扰动,我们认为细胞骨架变化可能与防止紧密贴附的细胞紧密排列以及抑制基底膜形成相关。共培养过程中支持细胞与管周细胞之间观察到的相互作用被假定类似于在器官发生过程中以及胎儿睾丸的小管形成过程中其他类型的间充质细胞 - 上皮细胞相互作用中发生的相互作用。推测地,dbcAMP对共培养系统中形态发生级联反应的阻断可能与其他人报道的dbcAMP对胎儿性腺器官培养中睾丸索形成的抑制有关。