Stuyvers Bruno D, Dun Wen, Matkovich Scot, Sorrentino Vincenzo, Boyden Penelope A, ter Keurs Henk E D J
Cardiovascular Research Group, Department of Medicine, Physiology and Biophysics, University of Calgary, Health Science Center/R1665, Calgary, Alberta, Canada.
Circ Res. 2005 Jul 8;97(1):35-43. doi: 10.1161/01.RES.0000173375.26489.fe. Epub 2005 Jun 9.
We have investigated the subcellular spontaneous Ca2+ events in canine Purkinje cells using laser scanning confocal microscopy. Three types of Ca2+ transient were found: (1) nonpropagating Ca2+ transients that originate directly under the sarcolemma and lead to (2) small Ca2+ wavelets in a region limited to 6-microm depth under the sarcolemma causing (3) large Ca2+ waves that travel throughout the cell (CWWs). Immunocytochemical studies revealed 3 layers of Ca2+ channels: (1) channels associated with type 1 IP3 receptors (IP3R1) and type 3 ryanodine receptors (RyR3) are prominent directly under the sarcolemma; (2) type 2 ryanodine receptors (RyR2s) are present throughout the cell but virtually absent in a layer between 2 and 4 microm below the sarcolemma (Sub-SL); (3) type 3 ryanodine receptors (RyR3) is the dominant Ca2+ release channel in the Sub-SL. Simulations of both nonpropagating and propagating transients show that the generators of Ca2+ wavelets differ from those of the CWWs with the threshold of the former being less than that of the latter. Thus, Purkinje cells contain a functional and structural Ca2+ system responsible for the mechanism that translates Ca2+ release occurring directly under the sarcolemma into rapid Ca2+ release in the Sub-SL, which then initiates large-amplitude long lasting Ca2+ releases underlying CWWs. The sequence of spontaneous diastolic Ca2+ transients that starts directly under the sarcolemma and leads to Ca2+ wavelets and CWWs is important because CWWs have been shown to cause nondriven electrical activity.
我们使用激光扫描共聚焦显微镜研究了犬浦肯野细胞中的亚细胞自发Ca2+事件。发现了三种类型的Ca2+瞬变:(1)非传播性Ca2+瞬变,直接起源于肌膜下方,导致(2)局限于肌膜下方6微米深度区域内的小Ca2+小波,进而引发(3)贯穿整个细胞传播的大Ca2+波(CWWs)。免疫细胞化学研究揭示了三层Ca2+通道:(1)与1型肌醇1,4,5-三磷酸受体(IP3R1)和3型兰尼碱受体(RyR3)相关的通道在肌膜正下方显著;(2)2型兰尼碱受体(RyR2s)存在于整个细胞中,但在肌膜下方2至4微米之间的一层中几乎不存在(肌膜下);(3)3型兰尼碱受体(RyR3)是肌膜下主要的Ca2+释放通道。对非传播性和传播性瞬变的模拟表明,Ca2+小波的产生源与CWWs的不同,前者的阈值低于后者。因此,浦肯野细胞含有一个功能性和结构性的Ca2+系统,负责将直接发生在肌膜下方的Ca2+释放转化为肌膜下快速的Ca2+释放机制,进而引发CWWs中大规模、持久的Ca2+释放。自发舒张期Ca2+瞬变从肌膜正下方开始,导致Ca2+小波和CWWs的序列很重要,因为CWWs已被证明会引起非驱动性电活动。