• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

钙信号转导、细胞凋亡与自噬在耳蜗发育中的作用:听觉获取的里程碑。

Ca signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition.

机构信息

Department of Physics and Astronomy "G. Galilei", University of Padua, 35131 Padua, Italy; Venetian Institute of Molecular Medicine (VIMM), Foundation for Advanced Biomedical Research, 35129 Padua, Italy; Department of Biomedical Sciences, Institute of Cell Biology and Neurobiology, Italian National Research Council, 00015 Monterotondo, (RM), Italy.

Department of Physics and Astronomy "G. Galilei", University of Padua, 35131 Padua, Italy; Venetian Institute of Molecular Medicine (VIMM), Foundation for Advanced Biomedical Research, 35129 Padua, Italy; Department of Biomedical Sciences, Institute of Protein Biochemistry, Italian National Research Council, 80131 Naples (NA), Italy.

出版信息

Cell Calcium. 2018 Mar;70:117-126. doi: 10.1016/j.ceca.2017.05.006. Epub 2017 May 11.

DOI:10.1016/j.ceca.2017.05.006
PMID:28578918
Abstract

In mammals, the sense of hearing arises through a complex sequence of morphogenetic events that drive the sculpting of the auditory sensory epithelium into its terminally functional three-dimensional shape. While the majority of the underlying mechanisms remain unknown, it has become increasingly clear that Ca signaling is at center stage and plays numerous fundamental roles both in the sensory hair cells and in the matrix of non-sensory, epithelial and supporting cells, which embed them and are tightly interconnected by a dense network of gap junctions formed by connexin 26 (Cx26) and connexin 30 (Cx30) protein subunits. In this review, we discuss the intricate interplay between Ca signaling, connexin expression and function, apoptosis and autophagy in the crucial steps that lead to hearing acquisition.

摘要

在哺乳动物中,听觉的产生是通过一系列复杂的形态发生事件驱动的,这些事件将听觉感觉上皮细胞塑造成其最终的三维功能形状。虽然大多数潜在的机制仍然未知,但越来越明显的是,钙信号处于中心地位,在感觉毛细胞和非感觉上皮和支持细胞基质中发挥着许多基本作用,这些细胞嵌入其中,并通过由连接蛋白 26(Cx26)和连接蛋白 30(Cx30)亚基形成的密集缝隙连接网络紧密相互连接。在这篇综述中,我们讨论了钙信号、连接蛋白表达和功能、细胞凋亡和自噬在导致听力获得的关键步骤中的复杂相互作用。

相似文献

1
Ca signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition.钙信号转导、细胞凋亡与自噬在耳蜗发育中的作用:听觉获取的里程碑。
Cell Calcium. 2018 Mar;70:117-126. doi: 10.1016/j.ceca.2017.05.006. Epub 2017 May 11.
2
Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.连接蛋白介导的非感觉细胞信号传导对小鼠耳蜗感觉性内毛细胞的发育至关重要。
J Neurosci. 2017 Jan 11;37(2):258-268. doi: 10.1523/JNEUROSCI.2251-16.2016.
3
Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs.豚鼠耳蜗感觉上皮中连接蛋白26和连接蛋白30的独特及梯度分布。
J Comp Neurol. 2006 Nov 20;499(3):506-18. doi: 10.1002/cne.21113.
4
A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.一种由双基因 Cx26(GJB2)和 Cx30(GJB6)突变引起的耳聋机制:通过损害耳蜗外侧壁中的异质缝隙连接功能来降低内耳电位。
Neurobiol Dis. 2017 Dec;108:195-203. doi: 10.1016/j.nbd.2017.08.002. Epub 2017 Aug 17.
5
Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals.内耳中的缝隙连接:不同脊椎动物分布模式的比较及哺乳动物中连接蛋白组成的评估
J Comp Neurol. 2003 Dec 8;467(2):207-31. doi: 10.1002/cne.10916.
6
Developmental regulation of TRPC3 ion channel expression in the mouse cochlea.鼠耳蜗中 TRPC3 离子通道表达的发育调控。
Histochem Cell Biol. 2010 Apr;133(4):437-48. doi: 10.1007/s00418-010-0686-x. Epub 2010 Mar 13.
7
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca Transients via a Gap Junction Characteristic of Developing Cochlea.GJB2 相关听力损失的体外模型通过发育耳蜗的缝隙连接特征再现钙瞬变。
Stem Cell Reports. 2016 Dec 13;7(6):1023-1036. doi: 10.1016/j.stemcr.2016.10.005. Epub 2016 Nov 10.
8
Pannexin1 channels dominate ATP release in the cochlea ensuring endocochlear potential and auditory receptor potential generation and hearing.泛连接蛋白1通道在耳蜗的三磷酸腺苷(ATP)释放中起主导作用,确保内淋巴电位和听觉感受器电位的产生以及听力。
Sci Rep. 2015 Jun 2;5:10762. doi: 10.1038/srep10762.
9
Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study.人类耳蜗感觉上皮细胞缝隙连接的分子组成和分布——超分辨率结构光照明显微镜(SR-SIM)研究。
Ups J Med Sci. 2017 Aug;122(3):160-170. doi: 10.1080/03009734.2017.1322645. Epub 2017 May 17.
10
Critical role of ATP-induced ATP release for Ca2+ signaling in nonsensory cell networks of the developing cochlea.ATP诱导的ATP释放对发育中耳蜗非感觉细胞网络中Ca2+信号传导的关键作用。
Proc Natl Acad Sci U S A. 2016 Nov 15;113(46):E7194-E7201. doi: 10.1073/pnas.1616061113. Epub 2016 Nov 2.

引用本文的文献

1
Unveiling the role of Na⁺/K⁺-ATPase pump: neurodegenerative mechanisms and therapeutic horizons.揭示钠钾ATP酶泵的作用:神经退行性机制与治疗前景
Pharmacol Rep. 2025 Jun;77(3):576-592. doi: 10.1007/s43440-025-00717-6. Epub 2025 Mar 21.
2
A pore locus in the E1 domain differentially regulates Cx26 and Cx30 hemichannel function.E1 结构域中的一个孔位差异调节 Cx26 和 Cx30 半通道功能。
J Gen Physiol. 2024 Nov 4;156(11). doi: 10.1085/jgp.202313502. Epub 2024 Sep 20.
3
A Protocol for the Automated Assessment of Cutaneous Pathology in a Mouse Model of Hemichannel Dysfunction.
一种用于评估半通道功能障碍的小鼠模型皮肤病理学的自动化评估方案。
Methods Mol Biol. 2024;2801:177-187. doi: 10.1007/978-1-0716-3842-2_13.
4
Damage-evoked signals in cochlear neurons and supporting cells.耳蜗神经元和支持细胞中的损伤诱发信号。
Front Neurol. 2024 Feb 14;15:1361747. doi: 10.3389/fneur.2024.1361747. eCollection 2024.
5
The critical role of cardiolipin in metazoan differentiation, development, and maturation.心磷脂在后生动物分化、发育和成熟中的关键作用。
Dev Dyn. 2023 Jun;252(6):691-712. doi: 10.1002/dvdy.567. Epub 2023 Feb 9.
6
and gene transcripts in the human cochlea: A study using RNAscope, confocal, and super-resolution structured illumination microscopy.以及人类耳蜗中的基因转录本:一项使用RNAscope、共聚焦和超分辨率结构照明显微镜的研究。
Front Mol Neurosci. 2022 Sep 20;15:973646. doi: 10.3389/fnmol.2022.973646. eCollection 2022.
7
Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca Signaling in Kölliker's Organ.连接蛋白26表达降低的小鼠听力获取失败与柯蒂氏器中凋亡相对于自噬的异常阶段以及ATP依赖性钙信号缺陷相关。
Front Cell Neurosci. 2022 Mar 3;16:816079. doi: 10.3389/fncel.2022.816079. eCollection 2022.
8
Connexin30-Deficiency Causes Mild Hearing Loss With the Reduction of Endocochlear Potential and ATP Release.连接蛋白30缺陷导致轻度听力损失,并伴有内淋巴电位降低和三磷酸腺苷释放减少。
Front Cell Neurosci. 2022 Jan 17;15:819194. doi: 10.3389/fncel.2021.819194. eCollection 2021.
9
Calcium Signaling Mediates Cell Death and Crosstalk with Autophagy in Kidney Disease.钙信号介导细胞死亡,并与肾脏病中的自噬相互作用。
Cells. 2021 Nov 17;10(11):3204. doi: 10.3390/cells10113204.
10
From spikes to intercellular waves: Tuning intercellular calcium signaling dynamics modulates organ size control.从尖峰到细胞间波:调节细胞间钙信号动力学可调节器官大小控制。
PLoS Comput Biol. 2021 Nov 1;17(11):e1009543. doi: 10.1371/journal.pcbi.1009543. eCollection 2021 Nov.