Tsay David, Dudman Joshua T, Siegelbaum Steven A
Department of Neuroscience, Columbia University, 1051 Riverside Drive, New York, NY 10032, USA.
Neuron. 2007 Dec 20;56(6):1076-89. doi: 10.1016/j.neuron.2007.11.015.
HCN1 hyperpolarization-activated cation channels act as an inhibitory constraint of both spatial learning and synaptic integration and long-term plasticity in the distal dendrites of hippocampal CA1 pyramidal neurons. However, as HCN1 channels provide an excitatory current, the mechanism of their inhibitory action remains unclear. Here we report that HCN1 channels also constrain CA1 distal dendritic Ca2+ spikes, which have been implicated in the induction of LTP at distal excitatory synapses. Our experimental and computational results indicate that HCN1 channels provide both an active shunt conductance that decreases the temporal integration of distal EPSPs and a tonic depolarizing current that increases resting inactivation of T-type and N-type voltage-gated Ca2+ channels, which contribute to the Ca2+ spikes. This dual mechanism may provide a general means by which HCN channels regulate dendritic excitability.
HCN1超极化激活阳离子通道对海马CA1锥体神经元远端树突的空间学习、突触整合以及长期可塑性起着抑制性限制作用。然而,由于HCN1通道可提供兴奋性电流,其抑制作用机制仍不清楚。在此我们报告,HCN1通道还可限制CA1远端树突Ca2+尖峰,而这与远端兴奋性突触处LTP的诱导有关。我们的实验和计算结果表明,HCN1通道既提供一种活性分流电导,可降低远端兴奋性突触后电位(EPSP)的时间整合,又提供一种持续性去极化电流,可增加T型和N型电压门控Ca2+通道的静息失活,而这些通道与Ca2+尖峰形成有关。这种双重机制可能是HCN通道调节树突兴奋性的一种普遍方式。