Currie Kevin P M, Fox Aaron P
Department of Neurobiology, Pharmacology and Physiology, University of Chicago, 947 E. 58th Street, MC 0926, Chicago, IL 60637, USA.
J Physiol. 2002 Mar 1;539(Pt 2):419-31. doi: 10.1113/jphysiol.2001.013206.
Inhibition of presynaptic voltage-gated calcium channels by direct G-protein betagamma subunit binding is a widespread mechanism that regulates neurotransmitter release. Voltage-dependent relief of this inhibition (facilitation), most likely to be due to dissociation of the G-protein from the channel, may occur during bursts of action potentials. In this paper we compare the facilitation of N- and P/Q-type Ca(2+) channels during short trains of action potential-like waveforms (APWs) using both native channels in adrenal chromaffin cells and heterologously expressed channels in tsA201 cells. While both N- and P/Q-type Ca(2+) channels exhibit facilitation that is dependent on the frequency of the APW train, there are important quantitative differences. Approximately 20 % of the voltage-dependent inhibition of N-type I(Ca) was reversed during a train while greater than 40 % of the inhibition of P/Q-type I(Ca) was relieved. Changing the duration or amplitude of the APW dramatically affected the facilitation of N-type channels but had little effect on the facilitation of P/Q-type channels. Since the ratio of N-type to P/Q-type Ca(2+) channels varies widely between synapses, differential facilitation may contribute to the fine tuning of synaptic transmission, thereby increasing the computational repertoire of neurons.
G蛋白βγ亚基直接结合对突触前电压门控钙通道的抑制是一种广泛存在的调节神经递质释放的机制。这种抑制的电压依赖性解除(易化),很可能是由于G蛋白从通道上解离,可能发生在动作电位爆发期间。在本文中,我们使用肾上腺嗜铬细胞中的天然通道和tsA201细胞中异源表达的通道,比较了在短串动作电位样波形(APW)期间N型和P/Q型Ca(2+)通道的易化情况。虽然N型和P/Q型Ca(2+)通道都表现出依赖于APW串频率的易化,但存在重要的定量差异。在一串刺激期间,约20%的N型I(Ca)的电压依赖性抑制被逆转,而P/Q型I(Ca)的抑制中有超过40%被解除。改变APW的持续时间或幅度会显著影响N型通道的易化,但对P/Q型通道的易化影响很小。由于N型和P/Q型Ca(2+)通道的比例在不同突触之间差异很大,差异性易化可能有助于突触传递的精细调节,从而增加神经元的计算能力。