Flucher B E, Andrews S B
Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
Cell Motil Cytoskeleton. 1993;25(2):143-57. doi: 10.1002/cm.970250204.
We have investigated the onset and maturation of action potential- and calcium-induced calcium release from the sarcoplasmic reticulum during the differentiation of excitation-contraction coupling in skeletal muscle. Microfluorometry and video imaging of cultured myotubes loaded with the fluorescent calcium indicator fluo-3 revealed the dynamics, time course, and physiological properties of calcium transients as well as their changes during development. Spontaneous and stimulated contractions in well-differentiated myotubes are accompanied by brief (200-500 ms) increases in the concentration of free cytoplasmic calcium. These transients are modulated by sub-threshold concentrations of caffeine, resulting in a plateau of elevated calcium. Two novel types of calcium transients were observed in non-contracting myotubes. 1) Fast localized transients (FLTs) are radially restricted focal release events that occur spontaneously within the myoplasm at various densities and frequencies. 2) Upon addition of caffeine, propagating calcium waves are generated (35-70 microns/s velocity), which are accompanied by contractures. Aside from caffeine sensitivity, calcium waves and contraction-related sustained release events are similar in amplitude and duration, as well as in their inactivation and refractory properties. Thus, these transients may represent calcium-induced calcium release in quiescent and active myotubes, respectively. Following one calcium-induced calcium release event, myotubes become refractory to new calcium-induced transients; however, action potential-induced transients and FLTs are not blocked. This suggests that these transients occur by distinct release mechanisms and that dual modes of calcium release exist prior to the coupling of calcium release to excitation.
我们研究了骨骼肌兴奋 - 收缩偶联分化过程中,动作电位和钙诱导的肌浆网钙释放的起始和成熟过程。对加载了荧光钙指示剂fluo - 3的培养肌管进行显微荧光测定和视频成像,揭示了钙瞬变的动力学、时间进程和生理特性,以及它们在发育过程中的变化。分化良好的肌管中的自发收缩和刺激收缩伴随着游离细胞质钙浓度的短暂(200 - 500毫秒)升高。这些瞬变受到亚阈值浓度咖啡因的调节,导致钙浓度升高并达到平台期。在不收缩的肌管中观察到两种新型钙瞬变。1)快速局部瞬变(FLTs)是在肌浆内以各种密度和频率自发发生的径向受限的局部释放事件。2)加入咖啡因后,会产生传播性钙波(速度为35 - 70微米/秒),并伴有挛缩。除了对咖啡因敏感外,钙波和与收缩相关的持续释放事件在幅度、持续时间以及失活和不应性特性方面相似。因此,这些瞬变可能分别代表静止和活跃肌管中的钙诱导钙释放。在一次钙诱导钙释放事件后,肌管对新的钙诱导瞬变变得不应期;然而,动作电位诱导的瞬变和FLTs不受阻断。这表明这些瞬变通过不同的释放机制发生,并且在钙释放与兴奋偶联之前存在两种钙释放模式。