Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh EH8 9XD, UK.
Cell Rep. 2018 Feb 13;22(7):1722-1733. doi: 10.1016/j.celrep.2018.01.069.
Cerebellar climbing-fiber-mediated complex spikes originate from neurons in the inferior olive (IO), are critical for motor coordination, and are central to theories of cerebellar learning. Hyperpolarization-activated cyclic-nucleotide-gated (HCN) channels expressed by IO neurons have been considered as pacemaker currents important for oscillatory and resonant dynamics. Here, we demonstrate that in vitro, network actions of HCN1 channels enable bidirectional glutamatergic synaptic responses, while local actions of HCN1 channels determine the timing and waveform of synaptically driven action potentials. These roles are distinct from, and may complement, proposed pacemaker functions of HCN channels. We find that in behaving animals HCN1 channels reduce variability in the timing of cerebellar complex spikes, which serve as a readout of IO spiking. Our results suggest that spatially distributed actions of HCN1 channels enable the IO to implement network-wide rules for synaptic integration that modulate the timing of cerebellar climbing fiber signals.
小脑 climbing-fiber 介导的复合峰源于下橄榄核(IO)中的神经元,对运动协调至关重要,是小脑学习理论的核心。IO 神经元表达的超极化激活环核苷酸门控(HCN)通道被认为是对振荡和共振动力学很重要的起搏电流。在这里,我们证明了在体外,HCN1 通道的网络作用使谷氨酸能突触反应具有双向性,而 HCN1 通道的局部作用决定了突触驱动动作电位的时间和波形。这些作用与 HCN 通道的拟议起搏功能不同,并且可能互补。我们发现,在行为动物中,HCN1 通道减少了小脑复合峰时间的可变性,作为 IO 放电的读出。我们的结果表明,HCN1 通道的空间分布作用使 IO 能够实现调制小脑 climbing 纤维信号时间的全网络突触整合规则。