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受精微观调控机制的研究进展:综述。

Research Progress on the Microregulatory Mechanisms of Fertilization: A Review.

机构信息

Department of Urology, People's Hospital of Beiliu, Beiliu, P. R. China.

Scientific Review Branch, Division of Extramural Research and Training, National Institute of Environmental Health Sciences, National Institutes of Health, Durham, NC, U.S.A.

出版信息

In Vivo. 2022 Sep-Oct;36(5):2002-2013. doi: 10.21873/invivo.12926.

DOI:10.21873/invivo.12926
PMID:36099087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9463889/
Abstract

The process of fertilization includes sperm capacitation, hyperactivation, an acrosome reaction and the release of acrosome enzymes, membrane fusion and channel formation, the release of the sperm nucleus, and gamete fusion. This process is closely related to the shape and vitality of the sperm, acrosome enzyme release, and the zona pellucida structure of the egg, as well as the opening and closing of various ion (e.g., calcium) channels, the regulation of signaling pathways such as cyclic adenosine monophosphate-protein kinase A, the release of progesterone, and the coupling of G-proteins. The interaction among multiple factors and their precise regulation give rise to multiple cascading regulatory processes. Problems with any factor will affect the success rate of fertilization. Recent studies have shown that with rapid societal development, the incidence of male infertility is increasing and occurs at younger ages. According to World Health Organization statistics, 15% of couples of childbearing ages have infertility problems, of which 50% are caused by male factors. Additionally, the cause of infertility cannot be identified in as many as 60% to 75% of male infertility patients. In this article, we review the research progress on the microregulation of fertilization and mechanisms underlying this process to identify causes and develop novel prevention and treatment strategies for male infertility.

摘要

受精过程包括精子获能、超激活、顶体反应和顶体酶释放、膜融合和通道形成、精子核释放以及配子融合。这个过程与精子的形态和活力、顶体酶释放以及卵子透明带的结构密切相关,还涉及各种离子(如钙)通道的开闭、环磷酸腺苷-蛋白激酶 A 信号通路的调节、孕酮的释放以及 G 蛋白的偶联。多种因素的相互作用及其精确调控产生了多个级联的调控过程。任何因素出现问题都会影响受精的成功率。最近的研究表明,随着社会的快速发展,男性不育的发病率正在增加,且发病年龄也越来越年轻。根据世界卫生组织的统计,15%的育龄夫妇存在不孕问题,其中 50%是由男性因素引起的。此外,多达 60%至 75%的男性不育患者的病因无法确定。本文就受精的微观调控及其机制的研究进展进行综述,以明确病因,并为男性不育症的防治提供新的策略。

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本文引用的文献

1
[Impact of sperm function on the fertilization rate of IVF].[精子功能对体外受精受精率的影响]
Zhonghua Nan Ke Xue. 2022 Jan;28(1):20-25.
2
Validation of a new multiparametric protocol to assess viability, acrosome integrity and mitochondrial activity in cooled and frozen thawed boar spermatozoa.验证一种新的多参数方案,用于评估冷却和冷冻解冻后猪精子的活力、顶体完整性和线粒体活性。
Cytometry B Clin Cytom. 2022 Sep;102(5):400-408. doi: 10.1002/cyto.b.22058. Epub 2022 Jan 31.
3
ACRBP (Sp32) is involved in priming sperm for the acrosome reaction and the binding of sperm to the zona pellucida in a porcine model.ACRBP(Sp32)参与猪模型中精子顶体反应的引发和与透明带的结合。
PLoS One. 2021 Jun 4;16(6):e0251973. doi: 10.1371/journal.pone.0251973. eCollection 2021.
4
Human Zona Pellucida Glycoproteins: Binding Characteristics With Human Spermatozoa and Induction of Acrosome Reaction.人透明带糖蛋白:与人精子的结合特性及顶体反应的诱导
Front Cell Dev Biol. 2021 Feb 11;9:619868. doi: 10.3389/fcell.2021.619868. eCollection 2021.
5
Molecular basis of egg coat cross-linking sheds light on ZP1-associated female infertility.卵壳交联的分子基础为 ZP1 相关女性不孕提供了线索。
Nat Commun. 2019 Jul 12;10(1):3086. doi: 10.1038/s41467-019-10931-5.
6
Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters.复合杂合性 ZP1 突变导致不孕姐妹的空卵泡综合征。
Hum Mutat. 2019 Nov;40(11):2001-2006. doi: 10.1002/humu.23864. Epub 2019 Jul 29.
7
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.ZP1、ZP2 和 ZP3 中的新型突变导致透明带形成异常,从而引起女性不孕。
Hum Genet. 2019 Apr;138(4):327-337. doi: 10.1007/s00439-019-01990-1. Epub 2019 Feb 27.
8
The serine protease testisin is present on the surface of capacitated stallion spermatozoa and interacts with key zona pellucida binding proteins.丝氨酸蛋白酶 testisin 存在于获能的种马精子表面,并与关键的透明带结合蛋白相互作用。
Andrology. 2019 Mar;7(2):199-212. doi: 10.1111/andr.12569. Epub 2018 Dec 13.
9
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.ZP3基因中的复发性错义突变导致空卵泡综合征和女性不孕。
Am J Hum Genet. 2017 Sep 7;101(3):459-465. doi: 10.1016/j.ajhg.2017.08.001.
10
Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility.ZP2和ZP3杂合突变的剂量效应导致人类不孕。
Hum Genet. 2017 Aug;136(8):975-985. doi: 10.1007/s00439-017-1822-7. Epub 2017 Jun 24.