Nguyen T, Chin W C, Verdugo P
Department of Bioengineering, University of Washington, Seattle 98195, USA.
Nature. 1998 Oct 29;395(6705):908-12. doi: 10.1038/27686.
Although fluctuations in cytosolic Ca2+ concentration have a crucial role in relaying intracellular messages in the cell, the dynamics of Ca2+ storage in and release from intracellular sequestering compartments remains poorly understood. The rapid release of stored Ca2+ requires large concentration gradients that had been thought to result from low-affinity buffering of Ca2+ by the polyanionic matrices within Ca2+-sequestering organelles. However, our results here show that resting luminal free Ca2+ concentration inside the endoplasmic reticulum and in the mucin granules remains at low levels (20-35 microM). But after stimulation, the free luminal [Ca2+] increases, undergoing large oscillations, leading to corresponding oscillations of Ca2+ release to the cytosol. These remarkable dynamics of luminal [Ca2+] result from a fast and highly cooperative Ca2+/K+ ion-exchange process rather than from Ca2+ transport into the lumen. This common paradigm for Ca2+ storage and release, found in two different Ca2+-sequestering organelles, requires the functional interaction of three molecular components: a polyanionic matrix that functions as a Ca2+/K+ ion exchanger, and two Ca2+-sensitive channels, one to import K+ into the Ca2+-sequestering compartments, the other to release Ca2+ to the cytosol.
尽管胞质Ca2+浓度的波动在细胞内传递信息中起着关键作用,但细胞内隔离区室中Ca2+的储存和释放动态仍知之甚少。储存的Ca2+的快速释放需要大的浓度梯度,人们曾认为这是由Ca2+隔离细胞器内的聚阴离子基质对Ca2+的低亲和力缓冲作用导致的。然而,我们在此的结果表明,内质网和粘蛋白颗粒内静息的腔内游离Ca2+浓度保持在低水平(20 - 35微摩尔)。但在刺激后,腔内游离[Ca2+]增加,经历大幅度振荡,导致向细胞质溶胶释放的Ca2+相应振荡。腔内[Ca2+]的这些显著动态是由快速且高度协同的Ca2+/K+离子交换过程而非Ca2+转运到腔内引起的。在两种不同的Ca2+隔离细胞器中发现的这种Ca2+储存和释放的常见模式,需要三种分子成分的功能相互作用:一种作为Ca2+/K+离子交换剂起作用的聚阴离子基质,以及两个Ca2+敏感通道,一个将K+导入Ca2+隔离区室,另一个将Ca2+释放到细胞质溶胶中。