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Endoplasmic reticulum protein 29 (ERp29), a protein related to sperm maturation is involved in sperm-oocyte fusion in mouse

机译:内质网蛋白29(ERp29)是一种与精子成熟有关的蛋白,参与小鼠精卵融合

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Background Sperm-oocyte fusion is a critical step in fertilization, which requires a series of proteins from both spermatozoa and oocyte to mediate membrane adhesion and subsequent fusion. A rat spermatozoa membrane protein is endoplasmic reticulum protein 29 (ERp29), which significantly increases on the sperm surface as well as in the cytoplasm of epididymal epithelia from caput to cauda as the sperm undergo epididymal maturation. Moreover, ERp29 facilitates viral infection via mediating membrane penetration. We determined if in addition to promoting sperm maturation ERp29 may also play a role in facilitating gamete fusion during the fertilization process. Methods Laser scanning confocal microscopy (LSCM) and Western blot analysis were employed to probe for ERp29 protein in BALB/c mouse epididymal and acrosome-reacted spermatozoa. We prepared rabbit polyclonal antibodies against mouse recombinant ERp29 (rERp29) to characterize: 1) fertilization rate (FR); 2) fertilization index (FI); 3) sperm motility and 4) acrosome reaction (AR). Results Confocal microscopy indicated that ERp29 was partially localized at the sperm head of the epididymal caput as well as over the whole head and part of the principal piece of the tail region from the epididymal cauda. However, when the acrosome reacted, ERp29 remained in the equatorial and post-acrosomal regions of the sperm head, which is the initial site of sperm-oocyte membrane fusion. Such localization changes were confirmed based on the results of Western blot analysis. Furthermore, the antibodies against mouse rERp29 inhibited the spermatozoa from penetrating into the zona pellucida (ZP)-free oocytes. The functional blocking antibodies reduced both mouse sperm-oocyte FR and FI at concentrations of 100 and 200 micro g/ml compared with pre-immunized rabbit IgG or with anti-mouse recombinant bactericidal/permeability-increasing protein (BPI, a sperm surface protein unrelated to sperm-oocyte fusion) antibodies (100 micro g/ml), but they had no effect on sperm motility and AR. Conclusion This study demonstrates that ERp29 on mouse spermatozoa membrane changes during epididymal transit and AR. Accordingly, in mice this protein may be one of the important factors involved in sperm fertilization by facilitating sperm-oocyte membrane fusion.
机译:背景技术精卵融合是受精的关键步骤,它需要精子和卵母细胞中的一系列蛋白质来介导膜的粘附和随后的融合。大鼠精子膜蛋白是内质网蛋白29(ERp29),当精子经历附睾成熟时,其在精子表面以及附睾上皮上皮细胞质中会显着增加。此外,ERp29通过介导膜渗透促进病毒感染。我们确定了ERp29除了促进精子成熟外是否还可以在受精过程中促进配子融合。方法采用激光扫描共聚焦显微镜(LSCM)和蛋白质印迹法检测BALB / c小鼠附睾和顶体反应的精子中ERp29蛋白的表达。我们制备了针对小鼠重组ERp29的兔多克隆抗体(rERp29),以表征:1)受精率(FR); 2)施肥指数(FI); 3)精子运动和4)顶体反应(AR)。结果共聚焦显微镜检查表明,ERp29部分位于附睾帽的精子头部,以及整个附睾尾部头部的整个头部和部分主要区域。但是,当顶体发生反应时,ERp29保留在精子头部的赤道和顶体区域,这是精卵细胞膜融合的初始位置。基于蛋白质印迹分析的结果证实了这种定位变化。此外,针对小鼠rERp29的抗体抑制了精子渗透到无透明带(ZP)的卵母细胞中。与预先免疫的兔IgG或抗小鼠重组杀菌/通透性增强蛋白(BPI,与精子表面蛋白无关)相比,功能性阻断抗体以100和200 micro g / ml的浓度降低了小鼠精卵FR和FI (精子/卵母细胞融合)抗体(100微克/毫升),但它们对精子活力和AR没有影响。结论本研究证明ERp29对小鼠附睾转运和AR过程中精子膜的改变。因此,在小鼠中,该蛋白可能是通过促进精卵细胞膜融合而参与精子受精的重要因素之一。

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