Alkon D L, Rasmussen H
Section on Neural Systems, National Institute of Neurologic and Communicative Disorders and Stroke, Bethesda, MD 20892.
Science. 1988 Feb 26;239(4843):998-1005. doi: 10.1126/science.2830669.
A spatial-temporal model of calcium messenger function is proposed to account for sustained cellular responses to sustained stimuli, as well as for the persistent enhancement of cell responsiveness after removal of a stimulus, that is, cellular memory. According to this model, spatial separation of calcium function contributes to temporal separation of distinct phases of the cellular response. At different cellular sites, within successive temporal domains, the calcium messenger is generated by different mechanisms and has distinct molecular targets. In particular, prolonged cell activation is brought about by the interaction of calcium with another spatially confined messenger, diacylglycerol, to cause the association of protein kinase C with the plasma membrane. Activity of the membrane-associated protein kinase C is controlled by the rate of calcium cycling across the plasma membrane. In some instances, a single stimulus induces both protein kinase C activation and calcium cycling and thus causes prolonged activation; but in others, a close temporal association of distinct stimuli brings about cell activation via interaction of these intracellular messengers. Persistent enhancement of cell responsiveness after removal of stimuli is suggested to be due to the continued association, or anchoring, of protein kinase C to the membrane.
提出了一种钙信使功能的时空模型,以解释细胞对持续刺激的持续反应,以及去除刺激后细胞反应性的持续增强,即细胞记忆。根据该模型,钙功能的空间分离有助于细胞反应不同阶段的时间分离。在连续的时间域内的不同细胞位点,钙信使由不同机制产生并具有不同的分子靶点。特别是,钙与另一种空间受限的信使二酰甘油相互作用,导致蛋白激酶C与质膜结合,从而引起细胞的长期激活。膜相关蛋白激酶C的活性受钙跨质膜循环速率的控制。在某些情况下,单一刺激既诱导蛋白激酶C激活又诱导钙循环,从而导致长期激活;但在其他情况下,不同刺激的紧密时间关联通过这些细胞内信使的相互作用引起细胞激活。去除刺激后细胞反应性持续增强被认为是由于蛋白激酶C与膜的持续结合或锚定。