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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
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Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions.缝隙连接蛋白 26 在耳蜗中的早期发育表达有助于其在耳蜗缝隙连接中占据主导功能作用。
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Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.连接蛋白30基因敲除小鼠和条件性连接蛋白26基因敲除小鼠在耳蜗中表现出不同的细胞变性模式和时间进程。
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Cx26 heterozygous mutations cause hyperacusis-like hearing oversensitivity and increase susceptibility to noise.Cx26 杂合突变导致类似听觉过敏的听力过度敏感,并增加对噪声的易感性。
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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。
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本文引用的文献

1
Gap junctions and cochlear homeostasis.缝隙连接与耳蜗内环境稳定
J Membr Biol. 2006 Feb-Mar;209(2-3):177-86. doi: 10.1007/s00232-005-0832-x. Epub 2006 May 17.
2
Prestin is expressed on the whole outer hair cell basolateral surface.Prestin在整个外毛细胞基底外侧表面均有表达。
Brain Res. 2006 Jun 20;1095(1):51-8. doi: 10.1016/j.brainres.2006.04.017. Epub 2006 May 18.
3
Gap junctional hemichannel-mediated ATP release and hearing controls in the inner ear.内耳中缝隙连接半通道介导的ATP释放与听力控制
Proc Natl Acad Sci U S A. 2005 Dec 20;102(51):18724-9. doi: 10.1073/pnas.0506481102. Epub 2005 Dec 12.
4
Connexin26 is responsible for anionic molecule permeability in the cochlea for intercellular signalling and metabolic communications.连接蛋白26负责耳蜗中阴离子分子的通透性,用于细胞间信号传导和代谢通讯。
Eur J Neurosci. 2005 Apr;21(7):1859-68. doi: 10.1111/j.1460-9568.2005.04031.x.
5
Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.由Cx26和30共同组装而成的耳蜗间隙连接比同源物表现出更快的细胞间Ca2+信号传导。
Am J Physiol Cell Physiol. 2005 Mar;288(3):C613-23. doi: 10.1152/ajpcell.00341.2004.
6
Cochlear function in Prestin knockout mice.耳蜗素敲除小鼠的耳蜗功能。
J Physiol. 2004 Nov 1;560(Pt 3):821-30. doi: 10.1113/jphysiol.2004.069559. Epub 2004 Aug 19.
7
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.
8
Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells.在HeLa细胞中表达的人连接蛋白26和30的通透性与门控特性
Biochem Biophys Res Commun. 2003 Jun 13;305(4):1024-33. doi: 10.1016/s0006-291x(03)00868-4.
9
Functional analysis of connexin-26 mutants associated with hereditary recessive deafness.与遗传性隐性耳聋相关的连接蛋白26突变体的功能分析。
J Neurochem. 2003 Feb;84(4):735-42. doi: 10.1046/j.1471-4159.2003.01555.x.
10
Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.连接蛋白26突变复合携带者的耳声发射和脑干诱发电位
Hear Res. 2003 Jan;175(1-2):140-51. doi: 10.1016/s0378-5955(02)00719-0.

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。

Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs.

作者信息

Zhao Hong-Bo, Yu Ning

机构信息

Department of Surgery-Otolaryngology, University of Kentucky Medical Center, Lexington, Kentucky 40536, USA.

出版信息

J Comp Neurol. 2006 Nov 20;499(3):506-18. doi: 10.1002/cne.21113.

DOI:10.1002/cne.21113
PMID:16998915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2553046/
Abstract

Connexin26 (Cx26) and Cx30 are predominant isoforms of gap junction channels in the cochlea and play a critical role in hearing. In this study, the cellular distributions of Cx26 and Cx30 in the cochlear sensory epithelium of guinea pigs were examined by immunofluorescent staining and confocal microscopy in whole mounts of the cochlear sensory epithelium and dissociated cell preparations. The expression of Cx26 and Cx30 demonstrated a longitudinal gradient distribution in the epithelium and was reduced threefold from the cochlear apex to base. The reduction was more pronounced in the Deiters cells and pillar cells than in the Hensen cells. Cx26 was expressed in all types of supporting cells, but little Cx30 labeling was seen in the Hensen cells. Cx26 expression in the Hensen cells was concentrated mainly in the second and third rows, forming a distinct band along the sensory epithelium at its outer region. In the dissociated Deiters cells and pillar cells, Cx30 showed dense labeling at the cell bodies and processes in the reticular lamina. Cx26 labeling largely overlapped that of Cx30 in these regions. Cx26 and Cx30 were also coexpressed in the gap junctional plaques between Claudius cells. Neither Cx26 nor Cx30 labeling was seen in the hair cells and spiral ganglion neurons. These observations demonstrate that Cx26 and Cx30 have a longitudinal gradient distribution and distinct cellular expression in the auditory sensory epithelium. This further supports our previous reports that Cx26 and Cx30 can solely and concertedly perform different functions in the cochlea.

摘要

连接蛋白26(Cx26)和Cx30是耳蜗中缝隙连接通道的主要亚型,在听力中起关键作用。在本研究中,通过免疫荧光染色和共聚焦显微镜,在耳蜗感觉上皮的整装片和分离细胞制剂中检测了豚鼠耳蜗感觉上皮中Cx26和Cx30的细胞分布。Cx26和Cx30的表达在上皮中呈纵向梯度分布,从耳蜗顶端到基部减少了三倍。这种减少在Deiters细胞和柱细胞中比在Hensen细胞中更明显。Cx26在所有类型的支持细胞中均有表达,但在Hensen细胞中几乎未见Cx30标记。Hensen细胞中Cx26的表达主要集中在第二和第三排,在感觉上皮的外侧区域沿其形成一条明显的带。在分离的Deiters细胞和柱细胞中,Cx30在网状层的细胞体和突起处显示密集标记。在这些区域,Cx26标记与Cx30的标记大部分重叠。Cx26和Cx30也在Claudius细胞之间的缝隙连接斑中共表达。在毛细胞和螺旋神经节神经元中均未见到Cx26和Cx30标记。这些观察结果表明,Cx26和Cx30在听觉感觉上皮中具有纵向梯度分布和独特的细胞表达。这进一步支持了我们之前的报道,即Cx26和Cx30可以单独和协同地在耳蜗中发挥不同的功能。