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为什么美洲有袋类动物的精子会形成成对的状态?来自对灰短尾负鼠(Monodelphis domestica)附睾中精子配对分析的线索。

Why do spermatozoa of American marsupials form pairs? A clue from the analysis of sperm-pairing in the epididymis of the grey short-tailed opossum, Monodelphis domestica.

作者信息

Taggart D A, Johnson J L, O'Brien H P, Moore H D

机构信息

Institute of Zoology, Zoological Society of London, United Kingdom.

出版信息

Anat Rec. 1993 Jul;236(3):465-78. doi: 10.1002/ar.1092360307.

DOI:10.1002/ar.1092360307
PMID:7689796
Abstract

In order to understand the evolutionary significance of sperm-pairing in American marsupials, an ultrastructural investigation was made of this process in the South American grey short-tailed opossum, Monodelphis domestica. One epididymis from each animal (5) was fixed for light and electron microscopy and divided into 18 segments. The contralateral tract was divided into similar segments and assessments made of the total number of spermatozoa and the proportion of sperm-pairs. The mean total sperm number was 4.20 +/- 0.62 x 10(6)/epididymis. Sperm-pairing commenced around segment 9 in the proximal corpus epididymidis and reached a maximum of 80% in the caudal sperm storage region of the duct. The sperm-pairing process was characterised by four stages. Spermatozoa exhibited parallel alignment as indicated by the positioning of identical cross-sections of sperm heads. This was followed by close apposition with acrosomal faces parallel rather than opposite. Rotation of the sperm heads around each other then apparently occurred as indicated by the morphological alignment of sections of paired sperm heads. Sperm-pairing was complete when the acrosomal faces were precisely aligned and joined. Misalignment and failure to pair was observed in about 20% of spermatozoa in the cauda epididymis. Such a complex sperm-pairing process may ensure that conjugated spermatozoa are precisely aligned so that flagella movement can be accurately coordinated for maximal progressive motility.

摘要

为了了解美洲有袋动物精子配对的进化意义,对南美灰短尾负鼠(Monodelphis domestica)的这一过程进行了超微结构研究。从每只动物(共5只)获取一个附睾,固定后用于光学显微镜和电子显微镜观察,并将其分为18段。对侧附睾也分为相似的段,并对精子总数和精子对的比例进行评估。附睾中精子的平均总数为4.20 +/- 0.62 x 10(6)/附睾。精子配对在附睾体近端的第9段左右开始,在附睾管尾部的精子储存区域达到最高80%。精子配对过程分为四个阶段。精子头部相同横截面的定位表明精子呈现平行排列。随后是顶体面平行而非相对的紧密贴靠。配对精子头部切片的形态排列表明,精子头部随后显然会相互旋转。当顶体面精确对齐并结合时,精子配对完成。在附睾尾部约20%的精子中观察到排列不齐和未能配对的情况。如此复杂的精子配对过程可能确保结合的精子精确对齐,以便鞭毛运动能够准确协调,实现最大程度的前进运动能力。

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