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顶体反应:透明带糖蛋白的相关性。

Acrosome reaction: relevance of zona pellucida glycoproteins.

机构信息

Reproductive Cell Biology Laboratory, National Institute of Immunology, New Delhi-110 067, India.

出版信息

Asian J Androl. 2011 Jan;13(1):97-105. doi: 10.1038/aja.2010.72. Epub 2010 Nov 1.

Abstract

During mammalian fertilisation, the zona pellucida (ZP) matrix surrounding the oocyte is responsible for the binding of the spermatozoa to the oocyte and induction of the acrosome reaction (AR) in the ZP-bound spermatozoon. The AR is crucial for the penetration of the ZP matrix by spermatozoa. The ZP matrix in mice is composed of three glycoproteins designated ZP1, ZP2 and ZP3, whereas in humans, it is composed of four (ZP1, ZP2, ZP3 and ZP4). ZP3 acts as the putative primary sperm receptor and is responsible for AR induction in mice, whereas in humans (in addition to ZP3), ZP1 and ZP4 also induce the AR. The ability of ZP3 to induce the AR resides in its C-terminal fragment. O-linked glycans are critical for the murine ZP3-mediated AR. However, N-linked glycans of human ZP1, ZP3 and ZP4 have important roles in the induction of the AR. Studies with pharmacological inhibitors showed that the ZP3-induced AR involves the activation of the G(i)-coupled receptor pathway, whereas ZP1- and ZP4-mediated ARs are independent of this pathway. The ZP3-induced AR involves the activation of T-type voltage-operated calcium channels (VOCCs), whereas ZP1- and ZP4-induced ARs involve both T- and L-type VOCCs. To conclude, in mice, ZP3 is primarily responsible for the binding of capacitated spermatozoa to the ZP matrix and induction of the AR, whereas in humans (in addition to ZP3), ZP1 and ZP4 also participate in these stages of fertilisation.

摘要

在哺乳动物受精过程中,卵母细胞周围的透明带(ZP)基质负责精子与卵母细胞的结合,并诱导 ZP 结合的精子发生顶体反应(AR)。AR 对于精子穿透 ZP 基质至关重要。小鼠的 ZP 基质由三种糖蛋白 ZP1、ZP2 和 ZP3 组成,而人类的 ZP 基质由四种(ZP1、ZP2、ZP3 和 ZP4)组成。ZP3 作为假定的主要精子受体,负责诱导小鼠的 AR,而在人类(除了 ZP3 之外),ZP1 和 ZP4 也诱导 AR。ZP3 诱导 AR 的能力存在于其 C 端片段中。O 连接聚糖对于小鼠 ZP3 介导的 AR 至关重要。然而,人类 ZP1、ZP3 和 ZP4 的 N 连接聚糖在诱导 AR 中也具有重要作用。药理学抑制剂的研究表明,ZP3 诱导的 AR 涉及 G(i)偶联受体途径的激活,而 ZP1 和 ZP4 介导的 AR 不依赖于该途径。ZP3 诱导的 AR 涉及 T 型电压门控钙通道(VOCCs)的激活,而 ZP1 和 ZP4 诱导的 AR 涉及 T 型和 L 型 VOCCs。总之,在小鼠中,ZP3 主要负责获能精子与 ZP 基质的结合和 AR 的诱导,而在人类(除了 ZP3 之外),ZP1 和 ZP4 也参与了这些受精阶段。

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