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大鼠螺旋韧带中钾离子通道超快速激活延迟整流钾通道信使核糖核酸的表达

Potassium channel ether à go-go mRNA expression in the spiral ligament of the rat.

作者信息

Lecain E, Sauvaget E, Crisanti P, Van Den Abbeele T, Huy P T

机构信息

Neurobiologie des réseaux sensorimoteurs, UPRESA 7060, Laboratoire d'Otologie Expérimentale, Faculté Lariboisière-St-Louis, Paris, France.

出版信息

Hear Res. 1999 Jul;133(1-2):133-8. doi: 10.1016/s0378-5955(99)00068-4.

Abstract

Identification of the K+ transporters located in the lateral wall of the cochlea is essential for a better understanding of the mechanisms by which a positive endocochlear potential and a high K+ concentration are achieved in endolymph. In this study, we have determined the distribution of the K+ channel rat ether à go-go (eag) mRNA in the cochlea. After reverse transcription of adult rat cochlear tissues, cDNA was amplified with primers specific to eag channel. The eag mRNA was localized in cochlear tissues by in situ hybridization using specific oligonucleotide probes tailed with digoxigenin conjugated UTP. Eag mRNA was detected in the organ of Corti but mainly in the fibrocytes of the spiral ligament but not in spiral prominence or in stria vascularis. The expression pattern of rat eag transcript in spiral ligament is complementary to the Na+,K+-ATPase distribution in the cochlear lateral wall. The localization of eag mRNA suggests that eag potassium channel may be produced in the corresponding cells. Considering the importance of the K+ gradient in the cochlea, the result reported here suggests that eag channel may play a role in the control of K+ fluxes in the spiral ligament.

摘要

识别位于耳蜗外侧壁的钾离子转运体对于更好地理解在内淋巴中实现内淋巴正电位和高钾离子浓度的机制至关重要。在本研究中,我们确定了钾离子通道大鼠外向整流钾通道(eag)mRNA在耳蜗中的分布。对成年大鼠耳蜗组织进行逆转录后,用针对eag通道的特异性引物扩增cDNA。使用与地高辛缀合的UTP尾的特异性寡核苷酸探针,通过原位杂交将eag mRNA定位在耳蜗组织中。在柯蒂氏器中检测到eag mRNA,但主要在螺旋韧带的纤维细胞中,而在螺旋凸或血管纹中未检测到。大鼠eag转录本在螺旋韧带中的表达模式与耳蜗外侧壁中钠钾ATP酶的分布互补。eag mRNA的定位表明eag钾通道可能在相应细胞中产生。考虑到耳蜗中钾离子梯度的重要性,此处报道的结果表明eag通道可能在控制螺旋韧带中的钾离子通量中发挥作用。

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