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调控小鼠精子顶体反应的 Liprin α3、LAR 及其配体

Regulation of acrosome reaction by Liprin α3, LAR and its ligands in mouse spermatozoa.

机构信息

Department of Gamete Immunobiology, National Institute for Research in Reproductive Health, Mumbai, India.

出版信息

Andrology. 2014 Mar;2(2):165-74. doi: 10.1111/j.2047-2927.2013.00167. Epub 2013 Dec 11.

Abstract

Zona pellucida-based induction of acrosome reaction (AR) is a popular and well-accepted hypothesis. However, this hypothesis is being challenged in recent years and it has been proposed that the cumulus cells might be the site of AR. In our previous study, we reported the presence of a synaptic protein Liprin α3 on sperm acrosome, and proposed its role in AR. This study was designed to understand the role of Liprin α3 and its interacting proteins in regulation of AR. It is observed that the presence of anti-Liprin α3 antibody inhibits the process of AR. Colocalization experiments demonstrate the coexistence of leucocyte antigen related (LAR) protein, Rab-interacting molecule (RIM) and Liprin α3 on sperm acrosome thereby completing the identification of all the members of RIM/MUNC/Rab3A/liprinα complex required for membrane fusion. This study demonstrates the effect of LAR ligands such as Syndecans, Nidogens and LAR wedge domain peptide on AR. We could see an increase in AR in presence of these ligands. On the basis of these data, we speculate that in presence of ligands or wedge peptide, LAR undergoes dimerization leading to inhibition of phosphatase activity and increase in AR. The presence of one of the ligands Syndecan-1 on cumulus cells led us to hypothesize that it is Syndecan which induces AR in vivo and thus another site of AR could lie in cumulus.

摘要

基于透明带的顶体反应(AR)诱导是一个流行且被广泛接受的假说。然而,近年来这一假说受到了挑战,有人提出卵丘细胞可能是 AR 的发生部位。在我们之前的研究中,我们报道了突触蛋白 Liprin α3 存在于精子顶体上,并提出了它在 AR 中的作用。本研究旨在了解 Liprin α3 及其相互作用蛋白在 AR 调节中的作用。研究发现,抗 Liprin α3 抗体的存在抑制了 AR 过程。共定位实验表明,白细胞相关抗原(LAR)蛋白、Rab 相互作用分子(RIM)和 Liprin α3 共同存在于精子顶体上,从而确定了膜融合所需的 RIM/MUNC/Rab3A/liprinα 复合物的所有成员。该研究表明了 Syndecans、Nidogens 和 LAR 楔形结构域肽等 LAR 配体对 AR 的影响。我们可以看到,在这些配体存在的情况下,AR 增加。基于这些数据,我们推测,在配体或楔形肽存在的情况下,LAR 发生二聚化,导致磷酸酶活性抑制和 AR 增加。卵丘细胞上存在一种配体 Syndecan-1,这使我们假设它是在体内诱导 AR 的配体,因此 AR 的另一个发生部位可能位于卵丘。

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