通过分解和清除控制附睾中的精子质量--对黄曲霉毒素处理过的大鼠异常精子的透射电子显微镜研究

K. Faisal, M. A. Akbarsha
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引用次数: 0

摘要

哺乳动物的附睾是一个动态器官,具有多种作用,其中包括精子质量控制,它似乎发生在附睾处理和储存过程中,以防止畸形精子大量出现在射精中。这种质量控制机制能够识别和清除死精/缺陷精子。在这方面,有报道称附睾分泌性小体/附睾小体所产生的致密基质的作用与死精子/缺陷精子的分解/溶解有关。本研究旨在探究精子各部分沿长度方向解体的机理细节是否包含相同或不同的模式。我们使用了黄曲霉毒素 B1 处理诱导成缺陷/不成活精子的实验大鼠模型的显微照片,对基质包埋的精子进行了细致筛查,结果显示主要部分(即头部、中段和鞭毛)的解体过程各不相同。头部的解体始于顶体的肿胀和裂解,随后是细胞核的逐渐解体。在中段,质膜首先解体,随后线粒体鞘和外密纤维(ODFs)解体。在鞭毛中,质膜和纤维鞘(FS)最初都没有任何解体的迹象。在解体过程中,精子头部、中段和鞭毛的走向不同,反映了各自的结构组成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Control of sperm quality in the epididymis by disintegration and removal – A transmission electron microscopy study of abnormal sperm of aflatoxin-treated rat
The mammalian epididymis is a dynamic organ endowed with diverse roles, including sperm quality control, which appears to occur during the epididymal processing and storage to prevent the misshapen spermatozoa from being present in the ejaculate in large numbers. This quality control mechanism is capable of identifying and removing dead/defective spermatozoa. In this respect, the role of a dense matrix arising from epididymal secretory aposomes/epididymosomes and associated disintegration/dissolution of dead/defective spermatozoa has been reported. This study was conceived to find if the mechanistic details of the disintegration of the parts of the spermatozoa along the length encompass the same or different patterns. We used photomicrographs from the experimental rat model induced into defective/unviable spermatozoa by aflatoxin B1 treatment. A meticulous screening of the matrix-embedded spermatozoa reflected different courses of disintegration of the major parts, namely, head, mid-piece, and flagellum. The disintegration of the head began with swelling of the acrosome and its lysis, followed by the gradual disintegration of the nucleus. In the mid-piece, the plasma membrane underwent disintegration first, and this was followed by disorganization and disintegration of the mitochondrial sheath and, subsequently, the outer dense fibers (ODFs). In the flagellum, neither the plasma membrane nor the fibrous sheath (FS) indicated any trace of disintegration initially. Rather, the FS and the plasma membrane were lifted off from the ODF-axoneme complex and, subsequently, with the FS remaining intact, the ODFs and the axonemal doublets on one side disintegrated, followed by disintegration of the remaining ODFs and the axonemal doublets. In the disintegration process, the spermatozoa’s head, mid-piece, and flagellum follow different courses, reflecting on the respective structural compositions.
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