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精子变形相关基因在少弱畸形精子症发生中的作用

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不孕不育是一种常见的疾病,影响大约10%~15%的育龄夫妇,其中男性因素占一半.通过精子发生产生形态与功能正常的精子是人类繁衍的基础.精子发生包括有丝分裂、减数分裂和精子变形三个阶段.其中,精子变形是雄性生殖细胞发育所特有的阶段,其相关基因的异常与少弱畸形精子症(oligoasthenoteratozoospermia,OAT)这一男性不育的常见类型密切相关.近年常有精子变形相关基因异常导致人或小鼠出现OAT表型的报道.但目前对于精子变形相关基因在OAT发生中的作用尚未有系统性的归纳.本文围绕精子变形中的关键事件及部分代表性的相关基因在OAT发生中的作用进行综述,希望对OAT患者的生育咨询、治疗和助孕提供更好的帮助.
The role of spermiogenesis-related genes in the occurrence of oligoasthenoteratozoospermia
Infertility is a major problem in human reproductive health.It is estimated that about 10%~15%of child-bearing couples worldwide are affected by infertility,with male factors accounting for half of these.The production of sperm with normal morphology and function is the basis of human reproduction.Spermatogenesis includes three stages:mitosis,meiosis and spermiogenesis.Among them,spermiogenesis is a unique stage of male germ cell development.Some studies have shown that defects of spermiogenesis-related genes are closely associated with oligoasthenoteratozoospermia(OAT),which is a common type of male infertility.In recent years,it has been reported that abnormalities in spermiogenesis-related genes lead to OAT phenotypes in humans and mice.However,the role of spermiogenesis-related genes in the development of OAT has not yet been systematically summarized.This review focuses on the key events in spermiogenesis and the roles of some representative related genes in the occurrence of OAT,in the hope of providing better assistance for fertility counselling,treatment,and pregnancy assistance for OAT-affected men.

spermiogenesisoligoasthenoteratozoospermiagene mutationmale infertility

胡童谣、涂超峰、谭跃球

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中南大学基础医学院生殖与干细胞工程研究所,长沙 410000

中信湘雅生殖与遗传专科医院,长沙 410000

精子变形 少弱畸形精子症 基因突变 男性不育

2024

中国科学(生命科学)
中国科学院

中国科学(生命科学)

CSTPCD北大核心
影响因子:0.725
ISSN:1674-7232
年,卷(期):2024.54(1)
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