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Multiple sequences in the C terminus of MaxiK channels are involved in expression, movement to the cell surface, and apical localization

机译:MaxiK通道C末端的多个序列参与表达,向细胞表面的移动和顶端定位

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摘要

Apical expression of the large-conductance, calcium- and voltage-activated potassium (MaxiK) channel in the cortical collecting duct is responsible for flow-stimulated potassium secretion. Here, we identify two cytoplasmic regions controlling apical expression of the MaxiK channel. Disruption of the proximal region results in the intracellular retention of the MaxiK channel without affecting channel assembly, thereby reducing surface expression. Coexpression of the WT channel with this mutant results in a reduction of WT MaxiK channel at the cell surface. Our data indicate that this proximal region is necessary for export of the MaxiK channel from the endoplasmic reticulum as a way to assess the final assembly of the channel. Deletion of a more distal region disrupts apical sorting, resulting in a nonpolarized distribution of the channel without impairing its surface delivery. In summary, we have found that sequences of amino acids in the C terminus of the MaxiK channel operate after the channel is assembled into a multimer and play a role in its expression, movement to the cell surface, and apical localization.
机译:皮质收集管中大电导,钙激活和电压激活的钾(MaxiK)通道的顶端表达是血流刺激钾分泌的原因。在这里,我们确定了两个控制MaxiK通道顶端表达的胞质区域。近端区域的破坏导致MaxiK通道的细胞内保留而不影响通道组装,从而降低表面表达。 WT通道与该突变体的共表达导致细胞表面WT MaxiK通道的减少。我们的数据表明,该近端区域对于从内质网输出MaxiK通道是必要的,以此作为评估通道最终组装的一种方法。删除更远端的区域会破坏根尖分类,导致通道的非极化分布,而不会损害其表面传递。总而言之,我们发现MaxiK通道C末端的氨基酸序列在该通道组装成多聚体后起作用,并在其表达,向细胞表面移动和顶端定位中起作用。

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