Neuhofer Wolfgang, Woo Seung Kyoon, Na Ki Young, Grunbein Rita, Park Won Kun, Nahm Ohnn, Beck Franz-X, Kwon H Moo
Physiologisches Institut der Universität München, D-80336 Münich, Germany.
Am J Physiol Cell Physiol. 2002 Dec;283(6):C1604-11. doi: 10.1152/ajpcell.00216.2002. Epub 2002 Jul 24.
In response to ambient hypertonicity, TonEBP (tonicity-responsive enhancer binding protein) stimulates certain genes including those encoding cytokines, transporters for organic solutes, and a molecular chaperone. TonEBP is regulated in a bidirectional manner, upregulated by an increase in ambient tonicity while downregulated by a decrease. To investigate the role of intracellular ionic strength in the activity of TonEBP, we subjected Madin-Darby canine kidney cells to a variety of conditions. Electron microprobe analysis was performed to measure intracellular electrolytes. Under conditions in which changes in cell volume were similar, TonEBP activity correlated with the intracellular ionic strength regardless of the external tonicity. On the other hand, inhibition of the Na+/K+-ATPase and high external K+ concentration led to a decreased activity of TonEBP despite a marked increase in the intracellular ionic strength. Because isotonic swelling is known to occur under these conditions, these data suggest that dilution of the cytoplasmic constituents inhibits the activity of TonEBP. We conclude that intracellular ionic strength and water content are major factors that determine the activity of TonEBP.
作为对环境高渗的反应,张力反应增强子结合蛋白(TonEBP)会刺激某些基因,包括那些编码细胞因子、有机溶质转运蛋白和一种分子伴侣的基因。TonEBP以双向方式受到调节,在环境张力增加时上调,而在张力降低时下调。为了研究细胞内离子强度在TonEBP活性中的作用,我们使Madin-Darby犬肾细胞处于多种条件下。进行电子微探针分析以测量细胞内电解质。在细胞体积变化相似的条件下,无论外部张力如何,TonEBP活性都与细胞内离子强度相关。另一方面,抑制Na+/K+-ATP酶和高浓度的外部钾离子会导致TonEBP活性降低,尽管细胞内离子强度显著增加。由于已知在这些条件下会发生等渗肿胀,这些数据表明细胞质成分的稀释会抑制TonEBP的活性。我们得出结论,细胞内离子强度和含水量是决定TonEBP活性的主要因素。