Györke S, Palade P
Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77550.
J Physiol. 1994 Apr 15;476(2):315-22. doi: 10.1113/jphysiol.1994.sp020133.
The mechanism of termination of Ca(2+)-induced Ca2+ release (CICR) from the sarcoplasmic reticulum has been investigated in voltage clamped cut crayfish muscle fibres loaded with rhod-2. During depolarizing steps evoking calcium current (ICa), Ca2+ release was first activated. Then the release rapidly (tau approximately 6 ms) declined, as evidenced by the rate of change of the intracellular fluorescence signal representing a Ca2+ transient. The rapid termination of release was not accounted for by inactivation of the trigger ICa or depletion of Ca2+ from the SR, since the rate at which release declined was constant under conditions where the rate of ICa inactivation and the amount of Ca2+ released varied widely. Pre-elevations of [Ca2+]i with prepulses or photolysis of caged Ca2+ caused depression of Ca2+ release during a subsequent test pulse. When the rate of ICa onset was varied by applying voltage ramps with different slopes, currents with fast onset elicited larger Ca2+ release than calcium currents with slower onset, even though the amplitude of the currents was the same. These results suggest that a Ca(2+)-dependent negative control mechanism exists which mediates the termination of CICR independently of the duration of the trigger ICa and before significant depletion of Ca2+ in the SR occurs.
在电压钳制的、加载了rhod-2的离体小龙虾肌纤维中,研究了肌浆网中钙诱导的钙释放(CICR)的终止机制。在诱发钙电流(ICa)的去极化步骤中,Ca2+释放首先被激活。然后,释放迅速(时间常数约为6毫秒)下降,这由代表Ca2+瞬变的细胞内荧光信号的变化率证明。释放的快速终止不能用触发ICa的失活或肌浆网中Ca2+的耗尽来解释,因为在ICa失活速率和释放的Ca2+量变化很大的条件下,释放下降的速率是恒定的。用预脉冲或笼锁Ca2+的光解预先提高[Ca2+]i会导致在随后的测试脉冲期间Ca2+释放减少。当通过施加不同斜率的电压斜坡来改变ICa起始速率时,即使电流幅度相同,起始快的电流比起始慢的钙电流引发更大的Ca2+释放。这些结果表明,存在一种Ca2+依赖性负调控机制,它独立于触发ICa的持续时间并在肌浆网中Ca2+显著耗尽之前介导CICR的终止。