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Lessons from mouse mutants of epithelial sodium channel and its regulatory proteins.

机译:小鼠上皮钠通道突变体及其调节蛋白的教训。

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摘要

The use of gene-modified mouse models allows the experimental in vivo analysis of specific gene defects at the level of target cells. With respect to the epithelial sodium channel and some of its regulatory proteins, gene-modified models that control gene defects in a time- and tissue-dependent conditional or constitutive manner have been generated. The combination of molecular and physiologic approaches in these mouse models increases the understanding of the complex regulation and the cell signaling cascades involved in Na(+) transport in target cells and may ultimately provide new insights into the pathophysiology of renal Na(+) retention and BP regulation. This review summarizes and discusses the gene-targeting approaches that have been applied to the epithelial sodium channel and its regulatory proteins.
机译:基因修饰的小鼠模型的使用允许在靶细胞水平上对特定基因缺陷进行实验性体内分析。关于上皮钠通道及其某些调节蛋白,已经产生了以时间和组织依赖性条件或组成方式控制基因缺陷的基因修饰模型。在这些小鼠模型中分子和生理学方法的结合增加了对复杂调节和靶细胞中Na(+)转运所涉及的细胞信号级联反应的理解,并最终可能为肾脏Na(+)保留和病理生理提供新的见解。 BP调节。这篇综述总结并讨论了已应用于上皮钠通道及其调节蛋白的基因靶向方法。

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