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柯萨奇病毒和腺病毒受体 (CXADR):最新发现及其在精子发生中的作用和调节。

Coxsackievirus and Adenovirus Receptor (CXADR): Recent Findings and Its Role and Regulation in Spermatogenesis.

机构信息

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

Adv Exp Med Biol. 2021;1288:95-109. doi: 10.1007/978-3-030-77779-1_5.

DOI:10.1007/978-3-030-77779-1_5
PMID:34453733
Abstract

Coxsackievirus and adenovirus receptor (CXADR) belongs to immunoglobulin superfamily of cell adhesion molecules. It expresses in most tissues, but displays unique and indispensable functions in some tissues such as heart and testis. CXADR is a multifunctional protein that can serve as a viral receptor, a junction structural protein and a signalling molecule. Thus, it exerts a wide range of functions such as facilitating leukocyte transmigration, regulating barrier function and cell adhesion, promoting EMT transition, and mediating spermatogenesis. This review aims to provide an overview and highlights some recent findings on CXADR in the field with emphasis on studies in the testis, upon which future studies can be designed to delineate the roles and regulation of CXADR in spermatogenesis.

摘要

柯萨奇病毒和腺病毒受体(CXADR)属于细胞黏附分子免疫球蛋白超家族。它在大多数组织中表达,但在某些组织中具有独特且不可或缺的功能,如心脏和睾丸。CXADR 是一种多功能蛋白,可作为病毒受体、连接结构蛋白和信号分子。因此,它发挥了广泛的功能,如促进白细胞迁移、调节屏障功能和细胞黏附、促进 EMT 转化以及介导精子发生。本综述旨在概述 CXADR 在该领域的最新研究进展,并重点介绍睾丸方面的研究,为未来研究设计提供依据,以阐明 CXADR 在精子发生中的作用和调节机制。

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Coxsackievirus and Adenovirus Receptor (CXADR): Recent Findings and Its Role and Regulation in Spermatogenesis.柯萨奇病毒和腺病毒受体 (CXADR):最新发现及其在精子发生中的作用和调节。
Adv Exp Med Biol. 2021;1288:95-109. doi: 10.1007/978-3-030-77779-1_5.
2
Mice depleted of the coxsackievirus and adenovirus receptor display normal spermatogenesis and an intact blood-testis barrier.缺乏柯萨奇病毒和腺病毒受体的小鼠表现出正常的精子发生过程以及完整的血睾屏障。
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本文引用的文献

1
Secondary Placental Defects in Mutant Mice.突变小鼠中的继发性胎盘缺陷
Front Physiol. 2019 May 29;10:622. doi: 10.3389/fphys.2019.00622. eCollection 2019.
2
Sertoli cell–specific coxsackievirus and adenovirus receptor regulates cell adhesion and gene transcription via β-catenin inactivation and Cdc42 activation.睾丸支持细胞特异性柯萨奇病毒和腺病毒受体通过β-连环蛋白失活和 Cdc42 激活调节细胞黏附和基因转录。
FASEB J. 2019 Jun;33(6):7588-7602. doi: 10.1096/fj.201801584R. Epub 2019 Mar 20.
3
CXADR-Mediated Formation of an AKT Inhibitory Signalosome at Tight Junctions Controls Epithelial-Mesenchymal Plasticity in Breast Cancer.
CXADR 介导的紧密连接处 AKT 抑制信号复合物的形成控制乳腺癌中的上皮-间充质转化。
Cancer Res. 2019 Jan 1;79(1):47-60. doi: 10.1158/0008-5472.CAN-18-1742. Epub 2018 Nov 1.
4
Coxsackievirus and Adenovirus Receptor, a Tight Junction Protein, in Peri-Implantation Mouse Embryos.柯萨奇病毒和腺病毒受体,一种紧密连接蛋白,在植入前小鼠胚胎中
Biol Reprod. 2016 Jul;95(1):5. doi: 10.1095/biolreprod.115.138099. Epub 2016 May 25.
5
Podocyte-Specific Deletion of Murine CXADR Does Not Impair Podocyte Development, Function or Stress Response.小鼠CXADR在足细胞中的特异性缺失不会损害足细胞的发育、功能或应激反应。
PLoS One. 2015 Jun 15;10(6):e0129424. doi: 10.1371/journal.pone.0129424. eCollection 2015.
6
Mice depleted of the coxsackievirus and adenovirus receptor display normal spermatogenesis and an intact blood-testis barrier.缺乏柯萨奇病毒和腺病毒受体的小鼠表现出正常的精子发生过程以及完整的血睾屏障。
Reproduction. 2014 Jun;147(6):875-83. doi: 10.1530/REP-13-0653. Epub 2014 Mar 13.
7
Synergistic effect of interferon-gamma and tumor necrosis factor-alpha on coxsackievirus and adenovirus receptor expression: an explanation of cell sloughing during testicular inflammation in mice.γ干扰素和肿瘤坏死因子-α对柯萨奇病毒和腺病毒受体表达的协同作用:对小鼠睾丸炎症期间细胞脱落的一种解释。
Biol Reprod. 2014 Mar 20;90(3):59. doi: 10.1095/biolreprod.113.113407. Print 2014 Mar.
8
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia.柯萨奇病毒和腺病毒受体是心肌缺血情况下心脏传导和心律失常易感性的调节因子。
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The Coxsackievirus and Adenovirus Receptor (CAR) undergoes ectodomain shedding and regulated intramembrane proteolysis (RIP).柯萨奇病毒和腺病毒受体 (CAR) 经历细胞外结构域脱落和调节的跨膜蛋白水解 (RIP)。
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An adenovirus vector incorporating carbohydrate binding domains utilizes glycans for gene transfer.一种腺病毒载体,包含碳水化合物结合结构域,利用聚糖进行基因转移。
PLoS One. 2013;8(2):e55533. doi: 10.1371/journal.pone.0055533. Epub 2013 Feb 1.