Williams D A, Becker P L, Fay F S
Science. 1987 Mar 27;235(4796):1644-8. doi: 10.1126/science.3103219.
The role of calcium in regulating the contractile state of smooth muscle has been investigated by measuring calcium and contraction in single smooth muscle cells with the calcium-sensitive dye fura-2 and the digital imaging microscope. The concentration of free calcium in the cytoplasm increased after stimulation of the cells by depolarization with high potassium or by application of carbachol. Changes in calcium always preceded contraction. The increase in calcium induced by these stimuli was limited to less than 1 microM. Calcium within the nucleus was also subject to a limitation of its rise during contraction. Intranuclear calcium rose from 200 nM at rest to no more than 300 nM while cytoplasmic calcium rose to over 700 nM. These apparent ceilings for both cytoplasmic and intranuclear calcium may result either from negative feedback of calcium on cytoplasmic and nuclear calcium channel gating mechanisms, respectively, or from the presence of calcium pumps that are strongly activated at the calcium ceilings.
通过使用钙敏染料fura-2和数字成像显微镜测量单个平滑肌细胞中的钙和收缩情况,研究了钙在调节平滑肌收缩状态中的作用。用高钾去极化或应用卡巴胆碱刺激细胞后,细胞质中游离钙的浓度增加。钙的变化总是先于收缩。这些刺激引起的钙增加限制在小于1微摩尔/升。细胞核内的钙在收缩过程中其升高也受到限制。核内钙从静息时的200纳摩尔/升升至不超过300纳摩尔/升,而细胞质钙则升至超过700纳摩尔/升。细胞质和核内钙的这些明显上限可能分别是由于钙对细胞质和核钙通道门控机制的负反馈,或者是由于在钙上限时被强烈激活的钙泵的存在。