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硫代糖脂固定蛋白1在小鼠精子头部的定位及作用

Localization and role of sulfoglycolipid immobilizing protein 1 on the mouse sperm head.

作者信息

Moase C E, Kamolvarin N, Kan F W, Tanphaichitr N

机构信息

Human IVF Laboratories, Loeb Medical Research Institute, Ottawa Civic Hospital, Ontario, Canada.

出版信息

Mol Reprod Dev. 1997 Dec;48(4):518-28. doi: 10.1002/(SICI)1098-2795(199712)48:4<518::AID-MRD13>3.0.CO;2-P.

Abstract

Sulfoglycolipid immobilizing protein 1 (SLIP 1) is an evolutionally conserved sperm head plasma membrane protein (M(r) = 68 kDa) that binds to sulfogalactosylglycerolipid (SGG), the major sulfoglycolipid present in mammalian sperm. The purpose of this study was to characterize the initial localization and the immunoaggregated relocalization of SLIP1 on the mouse sperm head. Direct immunofluorescence (DF) of live sperm using FITC-antiSLIP1 Fab fragments and FITC-antiSLIP1 IgG indicated that SLIP1 was present in the postacrosomal region of the sperm head, although the intensity of immunostaining by FITC-antiSLIP1 IgG was greatest at the border between the postacrosomal region and the acrosome. Unlike that observed with FITC-antiSLIP1 Fab, DF using FITC-antiSLIP1 IgG indicated that SLIP1 was also present in the anterior tip of the sperm head convex ridge. Results from electron microscopic studies, using antiSLIP1 IgG followed by protein A-gold on live mouse sperm, were similar to the DF findings. In contrast, indirect immunofluorescence (IIF) of live mouse sperm using antiSLIP1 IgG and FITC-secondary antibody IgG detected SLIP1 in the sperm head convex ridge only. The IIF and DF results strongly suggest that these bivalent antibodies could induce the sperm antigen relocalization on live sperm heads. SLIP1 redistribution may be dependent on availability of excess SGG, the SLIP1 binding ligand, based on the observation that purified exogenous biotinylated SLIP1 bound to live mouse sperm at both the postacrosomal and convex ridge regions of the mouse sperm head. Immunoaggregation induced by the primary antiSLIP1 IgG or antiSLIP1 Fab with secondary antibody IgG did not cause the acrosome reaction, suggesting that SLIP1 is not involved in sperm signal transduction. Furthermore, postacrosomal SLIP1 was shown to be involved in zona binding, since sperm pretreated with antiSLIP1 Fab fragments (100 micrograms/ml) bound to the egg zona pellucida in vitro at approximately 35% of control levels.

摘要

硫酸糖脂固定蛋白1(SLIP 1)是一种进化上保守的精子头部质膜蛋白(分子量=68 kDa),它与硫酸半乳糖基甘油脂(SGG)结合,SGG是哺乳动物精子中存在的主要硫酸糖脂。本研究的目的是表征SLIP1在小鼠精子头部的初始定位和免疫聚集后的重新定位。使用异硫氰酸荧光素(FITC)标记的抗SLIP1 Fab片段和FITC标记的抗SLIP1 IgG对活精子进行直接免疫荧光(DF)检测表明,SLIP1存在于精子头部顶体后区域,尽管FITC标记的抗SLIP1 IgG的免疫染色强度在顶体后区域与顶体之间的边界处最大。与使用FITC标记的抗SLIP1 Fab观察到的情况不同,使用FITC标记的抗SLIP1 IgG进行的DF检测表明,SLIP1也存在于精子头部凸嵴的前端。使用抗SLIP1 IgG然后在活小鼠精子上进行蛋白A-金标记的电子显微镜研究结果与DF结果相似。相比之下,使用抗SLIP1 IgG和FITC标记的二抗IgG对活小鼠精子进行间接免疫荧光(IIF)检测仅在精子头部凸嵴中检测到SLIP1。IIF和DF结果强烈表明,这些二价抗体可诱导活精子头部的精子抗原重新定位。基于纯化的外源性生物素化SLIP1在小鼠精子头部的顶体后和凸嵴区域均与活小鼠精子结合的观察结果,SLIP1的重新分布可能取决于过量的SLIP1结合配体SGG的可用性。由一抗抗SLIP1 IgG或抗SLIP1 Fab与二抗IgG诱导的免疫聚集未引起顶体反应,这表明SLIP1不参与精子信号转导。此外,顶体后SLIP1被证明参与与透明带的结合,因为用抗SLIP1 Fab片段(100微克/毫升)预处理的精子在体外与卵透明带的结合水平约为对照水平的35%。

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