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ErbB2 signaling in Schwann cells is mostly dispensable for maintenance of myelinated peripheral nerves and proliferation of adult Schwann cells after injury.雪旺细胞中的ErbB2信号传导对于维持有髓外周神经以及损伤后成年雪旺细胞的增殖大多是不必要的。
J Neurosci. 2006 Feb 15;26(7):2124-31. doi: 10.1523/JNEUROSCI.4594-05.2006.
2
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1A.1A型夏科-马里-图斯病患者雪旺细胞中ErbB2和ErbB3受体的过表达。
Muscle Nerve. 2006 Mar;33(3):342-9. doi: 10.1002/mus.20460.
3
Smaller inner ear sensory epithelia in Neurog 1 null mice are related to earlier hair cell cycle exit.Neurog 1基因敲除小鼠内耳感觉上皮较小与毛细胞更早退出细胞周期有关。
Dev Dyn. 2005 Nov;234(3):633-50. doi: 10.1002/dvdy.20551.
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LNX1 is a perisynaptic Schwann cell specific E3 ubiquitin ligase that interacts with ErbB2.LNX1是一种与突触周围施万细胞特异性相关的E3泛素连接酶,它与ErbB2相互作用。
Mol Cell Neurosci. 2005 Oct;30(2):238-48. doi: 10.1016/j.mcn.2005.07.015.
5
Diffusion and imaging properties of three new lipophilic tracers, NeuroVue Maroon, NeuroVue Red and NeuroVue Green and their use for double and triple labeling of neuronal profile.三种新型亲脂性示踪剂NeuroVue Maroon、NeuroVue Red和NeuroVue Green的扩散及成像特性及其在神经元形态双重和三重标记中的应用
Brain Res Bull. 2005 Aug 15;66(3):249-58. doi: 10.1016/j.brainresbull.2005.05.016.
6
Atoh1 null mice show directed afferent fiber growth to undifferentiated ear sensory epithelia followed by incomplete fiber retention.Atoh1基因敲除小鼠表现出传入纤维向未分化的耳感觉上皮定向生长,随后纤维保留不完全。
Dev Dyn. 2005 Jun;233(2):570-83. doi: 10.1002/dvdy.20370.
7
erbb3 and erbb2 are essential for schwann cell migration and myelination in zebrafish.Erbb3和Erbb2对斑马鱼施万细胞的迁移和髓鞘形成至关重要。
Curr Biol. 2005 Mar 29;15(6):513-24. doi: 10.1016/j.cub.2005.02.030.
8
Targeting c-erbB2 and other receptors of the c-erbB family: rationale and clinical applications.靶向c-erbB2及c-erbB家族的其他受体:理论依据与临床应用
J Chemother. 2004 Nov;16 Suppl 4:52-4. doi: 10.1179/joc.2004.16.Supplement-1.52.
9
The EGF receptor family as therapeutic targets in breast cancer.表皮生长因子受体家族作为乳腺癌的治疗靶点
Breast Dis. 2003;18:33-43. doi: 10.3233/bd-2003-18105.
10
Common and distinct elements in cellular signaling via EGF and FGF receptors.通过表皮生长因子(EGF)和成纤维细胞生长因子(FGF)受体进行细胞信号传导中的共同和独特要素。
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在缺乏ErbB2的情况下,内耳的神经支配仍处于紊乱状态。

A disorganized innervation of the inner ear persists in the absence of ErbB2.

作者信息

Morris Jacqueline K, Maklad Adel, Hansen Laura A, Feng Feng, Sorensen Christian, Lee Kuo-Fen, Macklin Wendy B, Fritzsch Bernd

机构信息

Department of Biology and Geology, Baldwin-Wallace College, Berea, OH 44017, USA.

出版信息

Brain Res. 2006 May 26;1091(1):186-99. doi: 10.1016/j.brainres.2006.02.090. Epub 2006 Apr 21.

DOI:10.1016/j.brainres.2006.02.090
PMID:16630588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3075922/
Abstract

ErbB2 protein is essential for the development of Schwann cells and for the normal fiber growth and myelin formation of peripheral nerves. We have investigated the fate of the otocyst-derived inner ear sensory neurons in the absence of ErbB2 using ErbB2 null mutants. Afferent innervation of the ear sensory epithelia shows numerous fibers overshooting the organ of Corti, followed by a reduction of those fibers in near term embryos. This suggests that mature Schwann cells do not play a role in targeting or maintaining the inner ear innervation. Comparable to the overshooting of nerve fibers, sensory neurons migrate beyond their normal locations into unusual positions in the modiolus. They may miss a stop signal provided by the Schwann cells that are absent as revealed with detailed histology. Reduction of overshooting afferents may be enhanced by a reduction of the neurotrophin Ntf3 transcript to about 25% of wild type. Ntf3 transcript reductions are comparable to an adult model that uses a dominant negative form of ErbB4 expressed in the supporting cells and Schwann cells of the organ of Corti. ErbB2 null mice retain afferents to inner hair cells possibly because of the prominent expression of the neurotrophin Bdnf in developing hair cells. Despite the normal presence of Bdnf transcript, afferent fibers are disoriented near the organ of Corti. Efferent fibers do not form an intraganglionic spiral bundle in the absence of spiral ganglia and appear reduced and disorganized. This suggests that either ErbB2 mediated alterations in sensory neurons or the absence of Schwann cells affects efferent fiber growth to the organ of Corti.

摘要

ErbB2蛋白对于施万细胞的发育以及外周神经的正常纤维生长和髓鞘形成至关重要。我们利用ErbB2基因敲除突变体研究了在缺乏ErbB2的情况下耳囊衍生的内耳感觉神经元的命运。耳感觉上皮的传入神经支配显示,许多纤维越过柯蒂氏器,随后在近期胚胎中这些纤维数量减少。这表明成熟的施万细胞在靶向或维持内耳神经支配方面不起作用。与神经纤维的过度延伸类似,感觉神经元迁移到其正常位置之外,进入蜗轴的异常位置。它们可能错过了施万细胞提供的停止信号,详细的组织学研究表明施万细胞不存在。神经营养因子Ntf3转录本减少至野生型的约25%,可能会增强传入纤维过度延伸的减少。Ntf3转录本的减少与一种成年模型相当,该模型使用在柯蒂氏器的支持细胞和施万细胞中表达的显性负性形式的ErbB4。ErbB2基因敲除小鼠保留了对内毛细胞的传入神经,这可能是因为发育中的毛细胞中神经营养因子Bdnf的显著表达。尽管Bdnf转录本正常存在,但传入纤维在柯蒂氏器附近方向紊乱。在没有螺旋神经节的情况下,传出纤维不会形成神经节内螺旋束,并且看起来数量减少且排列紊乱。这表明要么是ErbB2介导的感觉神经元改变,要么是施万细胞的缺失影响了传出纤维向柯蒂氏器的生长。