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甲状腺激素受体α1是外毛细胞最终分化过程中离子通道表达的关键调节因子。

Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells.

作者信息

Winter Harald, Braig Claudia, Zimmermann Ulrike, Engel Jutta, Rohbock Karin, Knipper Marlies

机构信息

Department of Otolaryngology, Tübingen Hearing Research Centre (THRC), Laboratory of Molecular Neurobiology and Cell Biology of the Inner Ear, University of Tübingen, Elfriede-Aulhorn-Strasse 5, 72076, Tübingen, Germany.

出版信息

Histochem Cell Biol. 2007 Jul;128(1):65-75. doi: 10.1007/s00418-007-0294-6. Epub 2007 May 23.

Abstract

Cochlear outer hair cells (OHCs) terminally differentiate prior to the onset of hearing. During this time period, thyroid hormone (TH) dramatically influences inner ear development. It has been shown recently that TH enhances the expression of the motor protein prestin via liganded TH receptor beta (TRbeta) while in contrast the expression of the potassium channel KCNQ4 is repressed by unliganded TRalpha1. These different mechanisms of TH regulation by TRalpha1 or TRbeta prompted us to analyse other ion channels that are required for the final differentiation of OHCs. We analysed the onset of expression of the Ca(2+) channel Ca(V)1.3, and the K(+) channels SK2 and BK and correlated the results with the regulation via TRalpha1 or TRbeta. The data support the hypothesis that proteins expressed in rodents prior to or briefly after birth like Ca(V)1.3 and prestin are either independent of TH (e.g. Ca(V)1.3) or enhanced through TRbeta (e.g. prestin). In contrast, proteins expressed in rodents later than P6 like KCNQ4 ( approximately P6), SK2 ( approximately P9) and BK ( approximately P11) are repressed through TRalpha1. We hypothesise that the precise regulation of expression of the latter genes requires a critical local TH level to overcome the TRalpha1 repression.

摘要

耳蜗外毛细胞(OHCs)在听力开始之前就已终末分化。在此期间,甲状腺激素(TH)对内耳发育有显著影响。最近的研究表明,TH通过与配体结合的甲状腺激素受体β(TRβ)增强运动蛋白prestin的表达,而相比之下,钾通道KCNQ4的表达则被未与配体结合的TRα1所抑制。TRα1或TRβ对TH的这些不同调节机制促使我们分析OHCs终末分化所需的其他离子通道。我们分析了Ca(2+)通道Ca(V)1.3、K(+)通道SK2和BK的表达起始,并将结果与通过TRα1或TRβ的调节相关联。数据支持这样的假设,即在出生前或出生后不久在啮齿动物中表达的蛋白质,如Ca(V)1.3和prestin,要么独立于TH(如Ca(V)1.3),要么通过TRβ增强(如prestin)。相比之下,在啮齿动物中出生后比P6晚表达的蛋白质,如KCNQ4(约P6)、SK2(约P9)和BK(约P11),则通过TRα1被抑制。我们假设,后一组基因表达的精确调节需要关键的局部TH水平来克服TRα1的抑制作用。

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