Lin M, Rodger J C
Cooperative Research Centre for Conservation and Management of Marsupials, Department of Biological Sciences, University of Newcastle, NSW, Australia.
J Anat. 1999 Feb;194 ( Pt 2)(Pt 2):223-32. doi: 10.1046/j.1469-7580.1999.19420223.x.
In certain Australian marsupials including the tammar wallaby (Macropus eugenii) and the brushtail possum (Trichosurus vulpecula), formation of the acrosome is not completed in the testis but during a complex differentiation process as spermatozoa pass through the epididymis. Using transmission and scanning electron microscopy this paper defined the process of acrosome formation in the epididymis, providing temporal and spatial information on the striking reorganisation of the acrosomal membranes and matrix and of the overlying sperm surface involved. On leaving the testis wallaby and possum spermatozoa had elongated 'scoop'-shaped acrosomes projecting from the dorsal surface of the head. During passage down the epididymis, this structure condensed into the compact button-like organelle found on ejaculated spermatozoa. This condensation was achieved by a complex process of infolding and fusion of the lateral projections of the 'scoop'. In the head of the epididymis the rims of the lateral scoop projections became shorter and thickened and folded inwards, to eventually meet midway along the longitudinal axis of the acrosome. As spermatozoa passed through the body of the epididymis the lateral projections fused together. Evidence of this fusion of the immature outer acrosomal membrane is the presence of vesicles within the acrosomal matrix which persist even in ejaculated spermatozoa. When spermatozoa have reached the tail of the epididymis the acrosome condenses into its mature form, as a small button-like structure contained within the depression on the anterior end of the nucleus. During the infolding process, the membranes associated with the immature acrosome are either engulfed into the acrosomal matrix (outer acrosomal membrane), or eliminated from the sperm head as tubular membrane elements (cytoplasmic membrane). Thus the surface and organelles of the testicular sperm head are transient structures in those marsupials with posttesticular acrosome formation and this must be taken into consideration in attempts to dissect the cell and molecular biology of fertilisation.
在某些澳大利亚有袋动物中,包括帚尾袋貂(Trichosurus vulpecula)和袋狸(Macropus eugenii),顶体的形成不是在睾丸中完成的,而是在精子通过附睾时的一个复杂分化过程中完成的。本文利用透射电子显微镜和扫描电子显微镜确定了附睾中顶体形成的过程,提供了顶体膜和基质以及相关精子表面显著重组的时间和空间信息。离开睾丸时,袋狸和帚尾袋貂的精子有细长的“勺状”顶体,从头部的背表面突出。在沿着附睾下行的过程中,这种结构浓缩成射精精子上发现的紧凑的纽扣状细胞器。这种浓缩是通过“勺”的侧向突起的复杂折叠和融合过程实现的。在附睾头部,侧向勺状突起的边缘变短、变厚并向内折叠,最终在顶体纵轴的中途相遇。当精子通过附睾体时,侧向突起融合在一起。未成熟顶体外膜融合的证据是顶体基质中存在小泡,即使在射精精子中也持续存在。当精子到达附睾尾部时,顶体浓缩成其成熟形式,成为包含在细胞核前端凹陷内的小纽扣状结构。在折叠过程中,与未成熟顶体相关的膜要么被吞噬到顶体基质中(顶体外膜),要么作为管状膜元件从精子头部消除(细胞质膜)。因此,在那些睾丸后顶体形成的有袋动物中,睾丸精子头部的表面和细胞器是短暂的结构,在试图剖析受精的细胞和分子生物学时必须考虑到这一点。