Blatter L A
Department of Physiology, Loyola University Chicago, Maywood, Illinois 60153.
Am J Physiol. 1995 Feb;268(2 Pt 1):C503-12. doi: 10.1152/ajpcell.1995.268.2.C503.
In vascular smooth muscle, binding of vasoactive substances to surface membrane receptors leads to a rise of intracellular cytoplasmic Ca2+ and to contraction. Cytoplasmic free Ca2+ concentration ([Ca2+]i) increases through release of Ca2+ from intracellular stores and Ca2+ entry through surface membrane ion channels. Membrane-permeant and membrane-impermeant forms of fura 2 were used to distinguish changes in intracellularly stored Ca2+ ([Ca2+]s) from changes in [Ca2+]i. The spatiotemporal patterns of the movement of Ca2+ between these two cellular compartments in cultured vascular smooth muscle cells (A7r5 cell line) were visualized with digital imaging fluorescence microscopy. The Ca2+ stores were localized by double staining with a fluorescent organelle-specific dye and the Ca2+ indicator. [Ca2+]s was measured after accumulation of the membrane-permeant form of fura 2 inside the stores and quenching of the fura 2 fluorescence in the cytoplasmic compartment with manganese. Stimulation with vasopressin led to a transient increase of [Ca2+]i and a concomitant decrease of [Ca2+]s. After stimulation with vasopressin, [Ca2+]i returned rapidly to normal resting levels, whereas the recovery of [Ca2+]s occurred on a much slower time scale. The refilling pathway of depleted stores involved Ca2+ entry into the bulk cytoplasmic compartment before uptake into the stores.
在血管平滑肌中,血管活性物质与表面膜受体结合会导致细胞内细胞质Ca2+浓度升高并引起收缩。细胞质游离Ca2+浓度([Ca2+]i)通过从细胞内储存库释放Ca2+以及通过表面膜离子通道进入Ca2+而增加。使用膜渗透性和非膜渗透性形式的fura 2来区分细胞内储存的Ca2+([Ca2+]s)的变化与[Ca2+]i的变化。用数字成像荧光显微镜观察培养的血管平滑肌细胞(A7r5细胞系)中Ca2+在这两个细胞区室之间移动的时空模式。通过用荧光细胞器特异性染料和Ca2+指示剂进行双重染色来定位Ca2+储存库。在用膜渗透性形式的fura 2在储存库内积累并在用锰淬灭细胞质区室中的fura 2荧光后测量[Ca2+]s。用血管加压素刺激导致[Ca2+]i短暂增加并伴随[Ca2+]s减少。用血管加压素刺激后,[Ca2+]i迅速恢复到正常静息水平,而[Ca2+]s的恢复发生在慢得多的时间尺度上。耗尽的储存库的重新填充途径涉及Ca2+在进入储存库之前进入大量细胞质区室。