Häring H U, Biermann E, Kemmler W
Am J Physiol. 1981 May;240(5):E556-65. doi: 10.1152/ajpendo.1981.240.5.E556.
The initial lag phase of insulin action on glucose transport in adipocytes reflects an unknown process that couples receptor binding and glucose transport activity. The influence of temperature, cellular ATP, cyclic AMP, and calcium on this process and a possible relation to internalization of insulin were studied. The Arrhenius plot of the coupling shows a break in slope at 30 degrees C; the activation energy below 30 degrees C is 17.5 kcal/mol. Reduction of cellular ATP by 70% prolongs the coupling process; initial binding and final maximal response of the glucose transport remain unaffected. Further reduction of ATP (greater than 90%) before addition of insulin abolishes the coupling completely. Reduction of ATP at different time points after addition of insulin blocks further activation; however, the actual state of activity is preserved. Calcium depletion by EDTA prolongs the coupling and decreases the maximal response. Internalization of insulin as determined in chloroquine-treated cells begins later than transport activation and is in contrast to transport activation not observable at 15 degrees C. In conclusion, the coupling is not related to internalization; it is ATP-dependent, whereas the initial binding and the activated transport system are ATP-independent. Calcium but not cyclic AMP might be second messenger or cofactor in the coupling process.
胰岛素对脂肪细胞葡萄糖转运作用的初始延迟期反映了一个未知过程,该过程将受体结合与葡萄糖转运活性联系起来。研究了温度、细胞内三磷酸腺苷(ATP)、环磷酸腺苷(cAMP)和钙对这一过程的影响以及与胰岛素内化的可能关系。耦合的阿伦尼乌斯图在30℃时斜率出现转折;30℃以下的活化能为17.5千卡/摩尔。细胞内ATP减少70%会延长耦合过程;葡萄糖转运的初始结合和最终最大反应不受影响。在添加胰岛素之前进一步降低ATP(超过90%)会完全消除耦合。在添加胰岛素后的不同时间点降低ATP会阻止进一步激活;然而,活性的实际状态得以保留。用乙二胺四乙酸(EDTA)耗尽钙会延长耦合并降低最大反应。在氯喹处理的细胞中测定的胰岛素内化开始时间晚于转运激活,并且与在15℃下未观察到的转运激活相反。总之,耦合与内化无关;它依赖于ATP,而初始结合和活化的转运系统不依赖于ATP。钙而非cAMP可能是耦合过程中的第二信使或辅助因子。