DiFrancesco D, Tortora P
Università di Milano, Dipartimento di Fisiologia e Biochimica Generali, Italy.
Nature. 1991 May 9;351(6322):145-7. doi: 10.1038/351145a0.
Cyclic AMP acts as a second messenger in the modulation of several ion channels that are typically controlled by a phosphorylation process. In cardiac pacemaker cells, adrenaline and acetylcholine regulate the hyperpolarization-activated current (if), but in opposite ways; this current is involved in the generation and modulation of pacemaker activity. These actions are mediated by cAMP and underlie control of spontaneous rate by neurotransmitters. Whether the cAMP modulation of if is mediated by channel phosphorylation is, however, still unknown. Here we investigate the action of cAMP on if in excised patches of cardiac pacemaker cells and find that cAMP activates if by a mechanism independent of phosphorylation, involving a direct interaction with the channels at their cytoplasmic side. Cyclic AMP activates if by shifting its activation curve to more positive voltages, in agreement with whole-cell results. This is the first evidence of an ion channel whose gating is dually regulated by voltage and direct cAMP binding.
环磷酸腺苷(cAMP)作为第二信使参与调节多种通常由磷酸化过程控制的离子通道。在心脏起搏细胞中,肾上腺素和乙酰胆碱以相反的方式调节超极化激活电流(If);该电流参与起搏活动的产生和调节。这些作用由cAMP介导,是神经递质控制自发心率的基础。然而,cAMP对If的调节是否由通道磷酸化介导仍不清楚。在这里,我们研究了cAMP对心脏起搏细胞切除膜片上If的作用,发现cAMP通过一种独立于磷酸化的机制激活If,该机制涉及cAMP与通道胞质侧的直接相互作用。与全细胞实验结果一致,环磷酸腺苷通过将其激活曲线向更正的电压方向移动来激活If。这是离子通道门控由电压和直接的cAMP结合双重调节的首个证据。