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首页> 外文期刊>The biochemical journal >Inwardly rectifying K+ channel Kir7.1 is highly expressed in thyroid follicular cells, intestinal epithelial cells and choroid plexus epithelial cells: implication for a functional coupling with Na+,K+-ATPase
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Inwardly rectifying K+ channel Kir7.1 is highly expressed in thyroid follicular cells, intestinal epithelial cells and choroid plexus epithelial cells: implication for a functional coupling with Na+,K+-ATPase

机译:内向整流性K +通道Kir7.1在甲状腺滤泡细胞,肠上皮细胞和脉络丛上皮细胞中高表达:与Na +,K + -ATPase功能偶联的意义

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摘要

pA novel inwardly rectifying Ksup+/sup channel, Kir7.1, with unique pore properties, was cloned recently. Working in the field of osmoregulation, we have also identified the same human and rat channel and found that the channel is unique not only in its pore sequence but also in its dense localization in the follicular cells of the thyroid gland. Northern blot analysis revealed that the channel message was abundantly expressed in the thyroid gland and small intestine, and moderately in the kidney, stomach, spinal cord and brain. Immunohistochemistry of the rat thyroid, intestine and choroid plexus demonstrated the expression of the channel protein in the follicular cells and epithelial cells, suggesting a role in the regulation of the ion-transporting functions of these specialized cells. The unique pore properties of Kir7.1 make it a strong candidate for the hypothetical low-conductance Ksup+/sup channel that is functionally coupled with Nasup+/sup,Ksup+/sup-ATPase by recycling Ksup+/sup. We therefore further examined the co-localization of Kir7.1 and Nasup+/sup,Ksup+/sup-ATPase and found that both are localized in the basolateral membrane of the thyroid follicular cell; in the choroid plexus, which is known to be unique in having Nasup+/sup,Ksup+/sup-ATPase in the apical side of the epithelial cells, Kir7.1 was found in the apical membrane, implying a close functional coupling between the channel and Nasup+/sup,Ksup+/sup-ATPase./p
机译:>最近克隆了具有独特孔特性的新型向内整流K + 通道Kir7.1。在渗透调节领域,我们还鉴定了相同的人和大鼠通道,发现该通道不仅在其孔序列上独特,而且在甲状腺滤泡细胞中的密集定位方面也是独特的。 Northern印迹分析显示该通道信息在甲状腺和小肠中大量表达,在肾脏,胃,脊髓和脑中中等表达。大鼠甲状腺,肠和脉络丛的免疫组织化学表明,通道蛋白在滤泡细胞和上皮细胞中表达,表明在调节这些专门细胞的离子转运功能中发挥了作用。 Kir7.1独特的孔特性使其成为假设的低电导K + 通道的强大候选者,该通道与Na + ,K + < / sup> -ATPase通过回收K + 。因此,我们进一步检查了Kir7.1和Na + ,K + -ATPase的共定位,发现两者均位于甲状腺滤泡细胞的基底外侧膜中。在脉络丛中,其独特之处在于其上皮细胞的顶端具有Na + ,K + -ATPase,在小鼠的脉络丛中发现Kir7.1顶端膜,暗示通道与Na + ,K + -ATPase之间紧密的功能偶联。

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