Zibirre R, Poronnik P, Koch G
J Cell Physiol. 1986 Oct;129(1):85-93. doi: 10.1002/jcp.1041290113.
Little is known concerning the effects of Na+-coupled solute transport on (Na+,K+)-ATPase mediated cation pumping in the intact cell. We investigated the effect of amino acid transport and growth factor addition on the short term regulation of (Na+,K+)-ATPase cation transport in HeLa cells. The level of pump activity in the presence of amino acids or growth factors was compared to the level measured in phosphate buffered saline. These rates were further related to the maximal pump capacity, operationally defined as ouabain inhibitable 86Rb+ influx in the presence of 15 microM monensin. Of the growth factors tested, only insulin was found to moderately (22%) increase (Na+,K+)-ATPase cation transport. The major determinant of pump activity was found to be the transport of amino acids. Minimal essential medium (MEM) amino acids increased ouabain inhibitable 86Rb+ influx to a level close to that obtained with monensin, indicating that the (Na+,K+)-ATPase is operating near maximal capacity during amino acid transport. This situation may apply to tissue culture conditions and consequently measurements of (Na+,K+)-ATPase activity in buffer solutions alone may yield little information about cation pumping under culture conditions. This finding applies especially to cells having high rates of amino acid transport. Furthermore, rates of amino acid transport may be directly or indirectly involved in the long-term regulation of the number of (Na+,K+)-ATPase molecules in the plasma membrane.
关于钠离子偶联溶质转运对完整细胞中(钠,钾)-ATP酶介导的阳离子泵浦作用的影响,目前所知甚少。我们研究了氨基酸转运和添加生长因子对HeLa细胞中(钠,钾)-ATP酶阳离子转运短期调节的影响。将存在氨基酸或生长因子时的泵活性水平与在磷酸盐缓冲盐溶液中测得的水平进行比较。这些速率进一步与最大泵浦能力相关,最大泵浦能力在操作上定义为在存在15微摩尔莫能菌素的情况下哇巴因可抑制的86铷流入量。在所测试的生长因子中,仅发现胰岛素能适度(22%)增加(钠,钾)-ATP酶阳离子转运。发现泵活性的主要决定因素是氨基酸的转运。最低必需培养基(MEM)氨基酸可使哇巴因可抑制的86铷流入量增加至接近莫能菌素所达到的水平,这表明在氨基酸转运过程中(钠,钾)-ATP酶接近最大能力运行。这种情况可能适用于组织培养条件,因此仅在缓冲溶液中测量(钠,钾)-ATP酶活性可能几乎无法提供有关培养条件下阳离子泵浦的信息。这一发现尤其适用于氨基酸转运速率高的细胞。此外,氨基酸转运速率可能直接或间接参与质膜中(钠,钾)-ATP酶分子数量的长期调节。