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肌醇1,4,5-三磷酸受体与钙网蛋白在人类精子赤道段及细胞质滴中膜结合囊泡内的共定位

Co-localization of the inositol 1,4,5-trisphosphate receptor and calreticulin in the equatorial segment and in membrane bounded vesicles in the cytoplasmic droplet of human spermatozoa.

作者信息

Naaby-Hansen S, Wolkowicz M J, Klotz K, Bush L A, Westbrook V A, Shibahara H, Shetty J, Coonrod S A, Reddi P P, Shannon J, Kinter M, Sherman N E, Fox J, Flickinger C J, Herr J C

机构信息

Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.

出版信息

Mol Hum Reprod. 2001 Oct;7(10):923-33. doi: 10.1093/molehr/7.10.923.

Abstract

Modulation of the intracellular calcium concentration within mammalian spermatozoa is important in several pre-fertilization events including hyperactivated motility and the acrosome reaction. To identify calcium binding proteins (CBP) potentially regulating these processes, a (45)Ca overlay technique was employed on 2-D blots of human sperm extracts. Microsequencing by Edman degradation and CAD mass spectrometry identified a relatively abundant 60.5 kDa CBP with a pI of 4.2 as calreticulin (CRT). Immunofluorescent labelling with anti-CRT antibodies localized CRT to the acrosome, with highest fluorescence in the equatorial segment, and in the cytoplasmic droplets of 94 and 48% of human spermatozoa respectively. Double immunolabelling experiments demonstrated co-localization of CRT and the inositol 1,4,5-trisphosphate receptor (IP(3)R) in the acrosome, in the equatorial segment, and vesicular structures in the cytoplasmic droplets of the neck region. Electron microscopic immunogold labelling localized CRT to the equatorial segment of acrosome-reacted spermatozoa and to membrane-enclosed vesicles within the cytoplasmic droplet of both acrosome-intact and acrosome-reacted spermatozoa. Localization of the IP(3) receptor to the CRT-containing vesicles, in the sperm neck and to the acrosome, suggests that capacitative calcium entry in human spermatozoa may be regulated from these putative calcium storage sites.

摘要

调节哺乳动物精子细胞内的钙浓度在包括超活化运动和顶体反应在内的几个受精前事件中很重要。为了鉴定可能调节这些过程的钙结合蛋白(CBP),采用了(45)Ca覆盖技术对人类精子提取物的二维印迹进行检测。通过埃德曼降解和CAD质谱进行的微量测序鉴定出一种相对丰富的60.5 kDa CBP,其pI为4.2,为钙网蛋白(CRT)。用抗CRT抗体进行免疫荧光标记将CRT定位到顶体,在赤道段荧光最强,分别在94%和48%的人类精子的细胞质滴中荧光最强。双重免疫标记实验表明,CRT与肌醇1,4,5-三磷酸受体(IP(3)R)在顶体、赤道段以及颈部细胞质滴中的囊泡结构中共定位。电子显微镜免疫金标记将CRT定位到顶体反应精子的赤道段以及顶体完整和顶体反应精子的细胞质滴内的膜包囊泡中。IP(3)受体在含有CRT的囊泡、精子颈部以及顶体中的定位表明,人类精子中的钙诱导性钙内流可能受这些假定的钙储存位点调控。

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