McCarron J G, McGeown J G, Reardon S, Ikebe M, Fay F S, Walsh J V
Biomedical Imaging Group, University of Massachusetts Medical Center, Worcester 01655.
Nature. 1992 May 7;357(6373):74-7. doi: 10.1038/357074a0.
Calcium entry through voltage-activated Ca2+ channels is important in regulating many cellular functions. Activation of these channels in many cell types results in feedback regulation of channel activity. Mechanisms linking Ca2+ channel activity with its downregulation have been described, but little is known of the events responsible for the enhancement of Ca2+ current that in many cells follows Ca2+ channel activation and an increase in cytoplasmic Ca2+ concentration. Here we investigate how this positive feedback is achieved in single smooth muscle cells. We find that in these cells voltage-activated calcium current is persistently but reversibly enhanced after periods of activation. This persistent enhancement of the Ca2+ current is mediated by activation of calmodulin-dependent protein kinase II because it is blocked when either the rise in cytoplasmic Ca2+ is inhibited or activation of calmodulin-dependent protein kinase II is prevented by specific peptide inhibitors of calcium-calmodulin or calmodulin-dependent protein kinase II itself. This mechanism may be important in different forms of Ca2+ current potentiation, such as those that depend on prior Ca2+ channel activation or are a result of agonist-induced release of Ca2+ from internal stores.
通过电压激活的Ca2+通道进入细胞的钙离子在调节多种细胞功能方面起着重要作用。在许多细胞类型中,这些通道的激活会导致通道活性的反馈调节。虽然已经描述了将Ca2+通道活性与其下调联系起来的机制,但对于在许多细胞中,在Ca2+通道激活和细胞质Ca2+浓度增加之后导致Ca2+电流增强的相关事件却知之甚少。在这里,我们研究了在单个平滑肌细胞中这种正反馈是如何实现的。我们发现,在这些细胞中,电压激活的钙电流在激活一段时间后会持续但可逆地增强。Ca2+电流的这种持续增强是由钙调蛋白依赖性蛋白激酶II的激活介导的,因为当细胞质Ca2+的升高受到抑制,或者钙调蛋白依赖性蛋白激酶II的激活被钙-钙调蛋白或钙调蛋白依赖性蛋白激酶II自身的特异性肽抑制剂阻止时,这种增强就会被阻断。这种机制可能在不同形式的Ca2+电流增强中起重要作用,比如那些依赖于先前Ca2+通道激活或由激动剂诱导从内部储存库释放Ca2+所导致的Ca2+电流增强。