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胞裂蛋白12在男性不育中的研究进展

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胞裂蛋白12(SEPT12)基因是胞裂蛋白基因(SEPTIN)家族的成员之一,在成年男性的睾丸组织中优势表达,在精子发生与成熟过程中发挥重要作用,对维持精子尾部结构的完整性至关重要.同时,SEPT12与精子形态异常密切相关,该基因突变导致男性生育力下降或男性不育.该文就SEPT12结构、生物学作用以及SEPT12突变导致男性不育症等方面进行研究进展的总结和展望.
SEPT 12 in male infertility:Advances in studies
SEPT1 2,as a member of the septin gene family,is preferentially expressed in the adult male testis and plays an im-portant role in the spermatogenesis and maturation of sperm.It is also essential for the maintenance of the structural integrity of the sperm tail.SEPT12 is closely related to sperm morphological abnormality,and its mutation leads to decreased fertility or infertility of males.This review presents an overview of the advances in and affords a prospect of the studies on the structure and biological functions of SEPT12 and the impact of its mutation on male fertility.

male fertilitySEPT1 2annulussperm morphological abnormality

陈海霞、张静、穆晓环、田文艳

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天津医科大学总医院妇产科生殖医学中心/天津市女性生殖健康与优生重点实验室,天津 300052

男性不育 胞裂蛋白12 精子环结构 精子形态异常

2024

中华男科学杂志
南京军区南京总医院

中华男科学杂志

CSTPCD
影响因子:1.052
ISSN:1009-3591
年,卷(期):2024.30(11)