Meza U, Bannister R, Melliti K, Adams B
Department of Physiology and Biophysics, University of Iowa, College of Medicine, Iowa City, Iowa 52242-1109, USA.
J Neurosci. 1999 Aug 15;19(16):6806-17. doi: 10.1523/JNEUROSCI.19-16-06806.1999.
Neuronal alpha1E subunits are thought to form R-type Ca channels. When expressed in human embryonic kidney cells with M2 muscarinic acetylcholine receptors, Ca channels encoded by rabbit alpha1E exhibit striking biphasic modulation. Receptor activation first produces rapid inhibition of current amplitude and activation rate. However, in the continued presence of agonist, alpha1E currents subsequently increase. Kinetic slowing persists during this secondary stimulation phase. After receptor deactivation, kinetic slowing is quickly relieved, and current amplitude over-recovers before returning toward control levels. These features indicate that inhibition and stimulation of alpha1E are separate processes, with stimulation superimposed on inhibition. Pertussis toxin eliminates inhibition without affecting stimulation, demonstrating that inhibition and stimulation involve distinct signaling pathways. Neither inhibition nor stimulation is altered by coexpression of Ca channel beta2a or beta3 subunits. Stimulation is abolished by staurosporine and reduced by intracellular 5'-adenylylimidodiphosphate, suggesting that phosphorylation is required. However, stimulation does not seem to involve cAMP-dependent protein kinase, protein kinase C, cGMP-dependent protein kinase, tyrosine kinases, or phosphoinositide 3-kinases. Stimulation does not require a Ca signal, because it is not specifically altered by varying intracellular Ca buffering or by substituting Ba as the charge carrier. In contrast to those formed by alpha1E, Ca channels formed by alpha1A or alpha1B display only inhibition and no stimulation during prolonged activation of M2 receptors. The dual modulation of alpha1E may confer unique physiological properties on native R-type Ca channels. As one possibility, R-type channels may continue to mediate Ca influx during steady inhibition of N-type and P/Q-type channels by muscarinic or other receptors.
神经元α1E亚基被认为可形成R型钙通道。当与M2毒蕈碱型乙酰胆碱受体一起在人胚肾细胞中表达时,兔α1E编码的钙通道表现出显著的双相调节。受体激活首先会快速抑制电流幅度和激活速率。然而,在激动剂持续存在的情况下,α1E电流随后会增加。在这个二次刺激阶段,动力学减慢持续存在。受体失活后,动力学减慢迅速缓解,电流幅度在恢复到对照水平之前会过度恢复。这些特征表明,α1E的抑制和刺激是分开的过程,刺激叠加在抑制之上。百日咳毒素消除了抑制作用而不影响刺激作用,这表明抑制和刺激涉及不同的信号通路。钙通道β2a或β3亚基的共表达既不改变抑制作用也不改变刺激作用。星形孢菌素可消除刺激作用,细胞内5'-腺苷酰亚胺二磷酸可降低刺激作用,这表明磷酸化是必需的。然而,刺激作用似乎不涉及cAMP依赖性蛋白激酶、蛋白激酶C、cGMP依赖性蛋白激酶、酪氨酸激酶或磷脂酰肌醇3激酶。刺激作用不需要钙信号,因为通过改变细胞内钙缓冲或用钡替代电荷载体,刺激作用不会发生特异性改变。与α1E形成的钙通道不同,在M2受体长时间激活期间,α1A或α1B形成的钙通道仅表现出抑制作用而无刺激作用。α1E的双相调节可能赋予天然R型钙通道独特的生理特性。一种可能性是,在毒蕈碱或其他受体对N型和P/Q型通道进行稳定抑制期间,R型通道可能继续介导钙内流。