Hypotonic induction of SGK1 and Na+ transport in A6 cells
Hypotonic induction of SGK1 and Na+ transport in A6 cells
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DOI：
10.1152/ajprenal.00176.2001
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发表时间：
2002-07-01
影响因子：
4.2
通讯作者：
Pearce, D
中科院分区：
文献类型：
--
作者：
Rozansky, DJ;Wang, J;Pearce, D
Serum and glucocorticoid-regulated kinase-1 (SGK1) is a serine-threonine kinase that is regulated at the transcriptional level by numerous regulatory inputs, including mineralocorticoids, glucocorticoids, follicle-stimulating hormone, and osmotic stress. In the distal nephron, SGK1 is induced by aldosterone and regulates epithelial Na(+) channel-mediated transepithelial Na(+) transport. In other tissues, including liver and shark rectal gland, SGK1 is regulated by hypertonic stress and is thought to modulate epithelial Na(+) channel- and Na(+)-K(+)-2Cl(-) cotransporter-mediated Na(+) transport. In this report, we examined the regulation of SGK1 mRNA and protein expression and Na(+) currents in response to osmotic stress in A6 cells, a cultured cell line derived from Xenopus laevis distal nephron. We found that in contrast to hepatocytes and rectal gland cells, hypotonic conditions stimulated SGK1 expression and Na(+) transport in A6 cells. Moreover, a correlation was found between SGK1 induction and the later phase of activation of Na(+) transport in response to hypotonic treatment. When A6 cells were pretreated with an inhibitor of phosphatidylinositol 3-kinase (PI3K), Na(+) transport was blunted and only inactive forms of SGK1 were expressed. Surprisingly, these results demonstrate that both hypertonic and hypotonic stimuli can induce SGK1 gene expression in a cell type-dependent fashion. Moreover, these data lend support to the view that SGK1 contributes to the defense of extracellular fluid volume and tonicity in amphibia by mediating a component of the hypotonic induction of distal nephron Na(+) transport.
