Su Xiaohua, Pang Tianxiang, Wakabayashi Shigeo, Shigekawa Munekazu
Department of Molecular Physiology, National Cardiovascular Center Research Institute, Fujishirodai 5-7-1, Suita, Osaka 565-8565, Japan.
Biochemistry. 2003 Feb 4;42(4):1086-94. doi: 10.1021/bi020427d.
We studied hyperosmolarity-induced changes in cell volume and cytoplasmic pH in PS120 cells expressing Na(+)/H(+) exchanger (NHE) isoforms and their mutants. Change in cell volume was estimated by measuring change in cell height by means of confocal microscopy. Regulatory volume increase (RVI) and cytoplasmic alkalinization were observed in cells expressing NHE1 but not in cells expressing NHE2 or NHE3. Studies using chimeric exchangers revealed that the membrane domain of the exchanger is responsible for the difference in volume sensitivity between NHE1 and NHE2. Although deletion or point mutation within the first extracellular loop of NHE1 did not affect RVI and alkalinization, point mutations within the corresponding region of NHE2, particularly a region containing aa 41-53, as well as replacement of the N-terminus of NHE2 with the corresponding region of NHE1, rendered NHE2 responsive to the activating effect of cell shrinkage. Thus, the membrane domain plays an important role in the response of the exchanger to cell shrinkage. The data suggest that the putative first extracellular loop of NHE2, but not that of NHE1, may exert an inhibitory influence on hyperosmolarity-induced activation of the exchanger and thereby block RVI.
我们研究了高渗诱导的表达钠/氢交换体(NHE)亚型及其突变体的PS120细胞的细胞体积和细胞质pH值变化。通过共聚焦显微镜测量细胞高度变化来估计细胞体积变化。在表达NHE1的细胞中观察到调节性容积增加(RVI)和细胞质碱化,而在表达NHE2或NHE3的细胞中未观察到。使用嵌合交换体的研究表明,交换体的膜结构域是NHE1和NHE2之间容积敏感性差异的原因。尽管NHE1第一个细胞外环内的缺失或点突变不影响RVI和碱化,但NHE2相应区域内的点突变,特别是包含第41-53位氨基酸的区域,以及用NHE1的相应区域替换NHE2的N端,使NHE2对细胞收缩的激活作用产生反应。因此,膜结构域在交换体对细胞收缩的反应中起重要作用。数据表明,NHE2而非NHE1的假定第一个细胞外环可能对高渗诱导的交换体激活产生抑制作用,从而阻断RVI。