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人精子中的 A-激酶锚定蛋白 4 前体(pro-AKAP4)。

A-kinase anchor protein 4 precursor (pro-AKAP4) in human spermatozoa.

机构信息

EA 4308 - GQG - Gametogenesis and Gamete Quality, University of Lille, Lille, France.

CHU Lille, Reproductive Biology - Spermiology - CECOS Institute, Lille, France.

出版信息

Andrology. 2018 Nov;6(6):854-859. doi: 10.1111/andr.12524. Epub 2018 Jul 8.

Abstract

BACKGROUND

A-kinase anchor protein 4 (AKAP4) and its precursor pro-AKAP4 are two major proteins in spermatozoa of rodents and mammals. Although researchers have characterized the AKAP4 expression in various species, the protein's expression in humans has not been described in detail.

OBJECTIVES

The objective of this study was to characterize human pro-AKAP4 more precisely (notably the definition of its localization and expression levels in human spermatozoa and testes).

MATERIALS AND METHODS

pro-AKAP4 protein expression levels were assessed by Western blotting. The pro-AKAP4's localization in spermatozoa and testes was determined using immunofluorescence staining and immunogold electron microscopy. Furthermore, pro-AKAP4 protein expression levels were assessed in a series of 77 human semen samples, and associations with semen parameters were evaluated.

RESULTS

Western blotting revealed a 100-kDa band in human sperm protein extracts. The pro-AKAP4 was immunolocalized in the fibrous sheath of the flagellum of ejaculated spermatozoa and in elongated spermatids in human testes. A Western blot analysis of 77 normozoospermic semen samples evidenced striking differences in pro-AKAP4 levels from one to another sample (median [interquartile range] integrated optical density = 305 [49-1038]). No correlations were found for pro-AKAP4 levels on one hand and semen volume, sperm concentration, sperm count, sperm motility, or sperm morphology on the other (p > 0.05 for all). However, pro-AKAP4 levels were positively correlated with motility after density gradient centrifugation of the semen (r = 0.224, p = 0.049).

DISCUSSION

AKAP4 protein might be activated as an alternative pathway to rescue sperm motility. In human spermatozoa, pro-AKAP4 might therefore be a 'reservoir' of mature AKAP4.

CONCLUSION

This study generated new knowledge about pro-AKAP4 in human semen, which may be of interest in the management of male infertility.

摘要

背景

A-激酶锚定蛋白 4(AKAP4)及其前体 pro-AKAP4 是啮齿动物和哺乳动物精子中的两种主要蛋白质。尽管研究人员已经对各种物种中的 AKAP4 表达进行了描述,但人类蛋白质的表达尚未详细描述。

目的

本研究旨在更精确地描述人源 pro-AKAP4(尤其是其在人类精子和睾丸中的定位和表达水平)。

材料和方法

通过 Western 印迹评估 pro-AKAP4 蛋白的表达水平。使用免疫荧光染色和免疫金电子显微镜确定 pro-AKAP4 在精子和睾丸中的定位。此外,在一系列 77 个人类精液样本中评估了 pro-AKAP4 蛋白的表达水平,并评估了与精液参数的相关性。

结果

Western 印迹显示人精子蛋白提取物中存在 100 kDa 条带。pro-AKAP4 免疫定位在射出精子鞭毛的纤维鞘中和人睾丸中伸长的精母细胞中。对 77 份正常精子精液样本的 Western blot 分析表明,样本之间 pro-AKAP4 水平存在显著差异(中位数[四分位距]积分光密度=305[49-1038])。pro-AKAP4 水平与精液量、精子浓度、精子计数、精子活力或精子形态之间均无相关性(所有 p 值均>0.05)。然而,pro-AKAP4 水平与精液密度梯度离心后的活力呈正相关(r=0.224,p=0.049)。

讨论

AKAP4 蛋白可能作为一种替代途径被激活,以挽救精子活力。因此,在人类精子中,pro-AKAP4 可能是成熟 AKAP4 的“储备库”。

结论

本研究为人类精液中的 pro-AKAP4 提供了新知识,这可能对男性不育症的治疗有意义。

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