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精子表面的分子生物学。睾丸后膜重塑。

The molecular biology of the sperm surface. Post-testicular membrane remodelling.

作者信息

Kirchhoff C, Pera I, Derr P, Yeung C H, Cooper T

机构信息

IHF Institute for Hormone and Fertility Research, University of Hamburg, Germany.

出版信息

Adv Exp Med Biol. 1997;424:221-32. doi: 10.1007/978-1-4615-5913-9_40.

Abstract

The membrane of testicular spermatozoa undergoes extensive changes in the epididymis, including rearrangement, modification and loss of pre-existing components, addition of new glycoproteins from epididymal secretions, and exchange of lipid constituents. As a result, the membrane of cauda epididymidal spermatozoa has a different composition and different properties, which collectively contribute to male fertility. Special significance has been attributed to sperm surface structures that only appear post-testicularly in the epididymis, the so-called "maturation antigens". Therefore, human post-testicular proteins have been cloned by substractive screening of epididymal cDNA libraries, employing testis as the primary negative control. To date, there is scanty information on their function and mechanism of deposition on the sperm surface. However, the major maturation antigen CD52 seems to bind firmly to the sperm membrane via its GPI anchor. Its synthesis is carefully regulated by the cells of the epididymal epithelium, with temperature and androgens acting synergistically on CD52 mRNA levels.

摘要

睾丸精子的膜在附睾中会发生广泛变化,包括已有成分的重排、修饰和丢失,附睾分泌物中新糖蛋白的添加以及脂质成分的交换。因此,附睾尾部精子的膜具有不同的组成和特性,这些共同对男性生育能力有贡献。附睾中仅在睾丸后出现的精子表面结构,即所谓的“成熟抗原”,具有特殊意义。因此,通过以睾丸作为主要阴性对照,对附睾cDNA文库进行消减筛选,克隆了人类睾丸后蛋白。迄今为止,关于它们在精子表面的功能和沉积机制的信息很少。然而,主要的成熟抗原CD52似乎通过其糖基磷脂酰肌醇(GPI)锚定牢固地结合在精子膜上。其合成受到附睾上皮细胞的严格调控,温度和雄激素协同作用于CD52 mRNA水平。

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