García-Ferreiro R E, Hernández-Ochoa E O, García D E
Departamento de Fisiología, Facultad de Medicina, UNAM, Mexico, DF, Mexico.
Pflugers Arch. 2001 Sep;442(6):848-58. doi: 10.1007/s004240100618.
The protein kinase C activator phorbol 12-myristate 13-acetate (PMA) has been used extensively in studies of G protein modulation of Ca2+ channels. PMA has been shown to be a powerful tool for inducing phosphorylation and interrupting G-protein-mediated signaling pathways. Here we re-examine the effects of PMA on whole-cell N-type Ca2+-channel currents in rat sympathetic neurons. We found that, along with an increase in the current amplitude previously reported by others, PMA pretreatment leads to alterations in current activation and inactivation kinetics. These alterations in current kinetics are voltage-dependent and are not reproduced by internal dialysis with the G protein inhibitor GDPbetaS. Alterations in current kinetics by PMA may therefore indicate the existence of a modulated state, presumably phosphorylated, of N-type Ca2+ channels. We propose that the increase in current amplitude is due primarily to alterations in current kinetics rather than to removal of tonic inhibition.
蛋白激酶C激活剂佛波酯12 -肉豆蔻酸酯13 -乙酸酯(PMA)已被广泛用于研究G蛋白对Ca2+通道的调节作用。PMA已被证明是一种诱导磷酸化和中断G蛋白介导的信号通路的有力工具。在此,我们重新研究了PMA对大鼠交感神经元全细胞N型Ca2+通道电流的影响。我们发现,除了其他人之前报道的电流幅度增加外,PMA预处理还会导致电流激活和失活动力学的改变。这些电流动力学的改变是电压依赖性的,并且用G蛋白抑制剂GDPβS进行内部透析无法重现。因此,PMA引起的电流动力学改变可能表明存在一种可能被磷酸化的N型Ca2+通道调节状态。我们提出,电流幅度的增加主要是由于电流动力学的改变,而不是由于去除了紧张性抑制。