Wright W W, Parvinen M, Musto N A, Gunsalus G L, Phillips D M, Mather J P, Bardin C W
Biol Reprod. 1983 Aug;29(1):257-70. doi: 10.1095/biolreprod29.1.257.
Experiments were conducted to determine how the cycle of the seminiferous epithelium influenced synthesis and secretion of proteins by seminiferous tubules. Tubular segments were treated with collagenase and then cultured with [35S]methionine. These myoid cell-depleted tubules isolated from different stages of the epithelial cycle exhibited, at Stages VI and XII, two distinct peaks of secretion of total radiolabeled proteins. Two-dimensional gel electrophoresis indicated that the patterns of secreted proteins from these two stages were remarkably different, while those from other stages were intermediate between those at the peaks. At least 15 proteins were secreted cyclically, many of them previously unrecognized products of the seminiferous epithelium. One product, designated Cyclic Protein-2 (CP-2), exhibited a pronounced cycle of secretion, its peak at Stage VI being 30-fold greater than at its nadir at Stages XII-XIV. Further investigation indicated that CP-2 did not appear to originate from myoid cells or dispersed germ cells but could be recovered from Sertoli cell-enriched cultures prepared from Stage VI tubules. Protein secretion by tubular segments was also characterized by immunoprecipitation with two polyspecific antisera directed against Sertoli cell products. Five secretory proteins were identified which had cycles different from one another and from CP-2. In contrast to secreted products, the synthesis of most cellular proteins by tubular segments remained relatively constant throughout the cycle. It is concluded: 1) segments of the seminiferous epithelium secrete proteins into the culture medium which are distinct from cellular proteins; 2) the synthesis of many of these proteins varies with the epithelial cycle; and 3) several of the secreted proteins are of Sertoli cell origin, including a newly identified protein, CP-2. This indicates that the morphology and the protein synthetic capacity of the seminiferous epithelium are coordinated over space and time.
进行实验以确定生精上皮周期如何影响生精小管中蛋白质的合成和分泌。将小管段用胶原酶处理,然后用[35S]甲硫氨酸培养。从上皮周期不同阶段分离的这些无肌样细胞的小管段在第VI和第XII阶段表现出两个不同的总放射性标记蛋白质分泌峰。二维凝胶电泳表明,这两个阶段分泌蛋白的模式明显不同,而其他阶段的模式介于两个峰之间。至少有15种蛋白质呈周期性分泌,其中许多是生精上皮以前未被识别的产物。一种产物,命名为循环蛋白-2(CP-2),表现出明显的分泌周期,其在第VI阶段的峰值比在第XII - XIV阶段的最低点高30倍。进一步研究表明,CP-2似乎不是起源于肌样细胞或分散的生殖细胞,而是可以从第VI阶段小管制备的富含支持细胞的培养物中回收。小管段的蛋白质分泌也通过用两种针对支持细胞产物的多特异性抗血清进行免疫沉淀来表征。鉴定出五种分泌蛋白,它们的周期彼此不同且与CP-2不同。与分泌产物相反,小管段中大多数细胞蛋白的合成在整个周期中保持相对恒定。得出以下结论:1)生精上皮段将与细胞蛋白不同的蛋白质分泌到培养基中;2)许多这些蛋白质的合成随上皮周期而变化;3)几种分泌蛋白起源于支持细胞,包括一种新鉴定的蛋白质CP-2。这表明生精上皮的形态和蛋白质合成能力在空间和时间上是协调的。