顶体:比较形态和发育,对人类家族性全球精子症病例的贡献报告。

Journal de la Societe de biologie Pub Date : 2008-01-01 Epub Date: 2008-06-13 DOI:10.1051/jbio:2008016
Isabelle Koscinski, Anne Sophie Jaeger, Céline Moutou, Stéphane Viville
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引用次数: 1

摘要

精子顶体在大多数被研究的动物物种的受精中起着重要作用。一般说来,在水相受精发生后,顶体立即出现。顶体的生化成分及其释放方式表明它是一种简单的溶酶体。但这将忽略其在精子发生中重要的形态形成作用。它的发展与微管manchette系统的发展密切相关。动物诱变的分子数据有助于理解顶体的生物发生机制。球形精子症是一种罕见但严重的人类畸形精子症,其特征是射精完全由缺乏顶体的圆头精子组成。它起源于一个受干扰的顶体生物发生。最近,一项家族性球形精子症的遗传研究突出了与球形精子表型相关的基因SPATA16的纯合子突变。这项研究有助于理解人类顶体形成的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The acrosome: comparative morphology and development, contribution of a human familial globozoospermia case report].

Sperm acrosome is known to play a role in the fertilization of the majority of animal species studied. As a general rule, the acrosome appeared as soon as the fertilization occurred out of aquaeous phase. The biochemical content of acrosome as well as its release mode could suggest it is a simple lysosome. But this would by pass its important morphogenic role in spermiogenesis. Its development is strongly linked to the development of the microtubules manchette system. Molecular data of animal mutagenesis contribute to the understanding of acrosome biogenesis mechanisms. Globozoospermia is a rare but severe human teratozoospermia, characterized by ejaculates entirely consisting of round-headed spermatozoa that lack an acrosome. It originates from a disturbed acrosome biogenesis. Recently, the genetic study of a familial globozoospermia led to highlight a homozygote mutation of the gene SPATA16, linked to the globozoospermic phenotype. This study contributes to the understanding of the mechanisms implied in human acrosome formation.

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