Phillips D M, Jones R, Shalgi R
Population Council, New York, NY 10021.
Mol Reprod Dev. 1991 Aug;29(4):347-56. doi: 10.1002/mrd.1080290406.
The surface membrane of mammalian spermatozoa is known to undergo considerable conformational and organizational changes during epididymal maturation. However, much less is known about remodelling of intracellular membranes. In this communication we have used specific immunological markers to study the behavior of several antigens both on and within rat spermatozoa as they mature in the epididymis. Four monoclonal antibodies (McAbs) designated 5B1, 1B5, 2D6, and 1B6 were used to probe testicular and caput and cauda epididymal spermatozoa by indirect immunofluorescence and immunogold labeling techniques. None of the McAbs bound to testicular spermatozoa; in all cases, they became reactive only on spermatozoa which had reached the caput epididymis. McAb 5B1 was restricted to the outer acrosomal membrane (OAM) of the acrosomal cap domain. The epitope first appeared on antigen(s) with molecular mass (Mr) of approximately 200 kDa in immature spermatozoa, but later in mature spermatozoa the antigen(s) had Mr of approximately 160 kDa. The antigen(s) recognized by 1B5 McAb on the other hand was initially distributed over the OAM of the entire acrosomal domain (cap + equatorial segment), but during maturation it became progressively more restricted in area until in cauda spermatozoa only the anterior tip of the OAM bound the McAb. McAb 2D6 also bound to the entire OAM and acrosomal contents of caput spermatozoa, but, unlike 5B1 and 1B5 McAbs, reactivity was transient. That is, staining was first detected in caput spermatozoa but then disappeared in corpus and cauda spermatozoa. In contrast to all of the above, 1B6 McAb bound to the surface membrane overlying the entire head domain of caput spermatozoa, but during maturation it became restricted to the postacrosomal domain. These results indicate that, in addition to remodeling of the surface membrane during epididymal maturation, extensive processing of intracellular membrane antigens also takes place and that it is very active within the acrosome. The nature of these intracellular processing events remains to be elucidated, but they may have important consequences for membrane fusion and cell recognition phenomena during fertilization.
已知哺乳动物精子的表面膜在附睾成熟过程中会经历相当大的构象和组织变化。然而,关于细胞内膜重塑的了解却少得多。在本通讯中,我们使用特异性免疫标记物来研究大鼠精子在附睾中成熟时表面和内部几种抗原的行为。使用四种单克隆抗体(McAbs),分别命名为5B1、1B5、2D6和1B6,通过间接免疫荧光和免疫金标记技术检测睾丸、附睾头和附睾尾精子。没有一种McAb与睾丸精子结合;在所有情况下,它们仅在到达附睾头的精子上具有反应性。McAb 5B1局限于顶体帽区域的顶体外膜(OAM)。该表位最初出现在未成熟精子中分子量(Mr)约为200 kDa的抗原上,但在成熟精子中,该抗原的Mr约为160 kDa。另一方面,1B5 McAb识别的抗原最初分布在整个顶体区域(帽 + 赤道段)的OAM上,但在成熟过程中,其分布区域逐渐受到限制,直到在附睾尾精子中只有OAM的前端与McAb结合。McAb 2D6也与附睾头精子的整个OAM和顶体内容物结合,但与5B1和1B5 McAbs不同,其反应性是短暂的。也就是说,染色首先在附睾头精子中检测到,但随后在附睾体和附睾尾精子中消失。与上述所有情况相反,1B6 McAb与附睾头精子整个头部区域上方的表面膜结合,但在成熟过程中它局限于顶体后区域。这些结果表明,除了附睾成熟过程中表面膜的重塑外,细胞内膜抗原也发生了广泛的加工,并且在顶体内非常活跃。这些细胞内加工事件的性质仍有待阐明,但它们可能对受精过程中的膜融合和细胞识别现象产生重要影响。