Input-specific bidirectional regulation of hippocampal CA3 pyramidal cell excitability

输入特异性双向调节海马CA3锥体细胞兴奋性

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Abstract

High-frequency mossy fibre (MF) inputs trigger a sustained increase in excitability to perforant pathway (PP) inputs in CA3 pyramidal cells (CA3-PC) by reducing Kv1.2 levels at distal apical dendrites, known as long-term potentiation of intrinsic excitability (LTP-IE). LTP-IE enhances excitatory postsynaptic potential (EPSP)-to-spike coupling at PP synapses, facilitating Hebbian LTP of synaptic weights. Prolonged hyperexcitability is detrimental, yet it is little understood how LTP-IE is restored in CA3-PCs. Here we show that MF-induced LTP-IE can be reversed through the burst firing of a CA3-PC elicited by PP or recurrent synaptic inputs. This reversal was impeded by the oxidative bias of cellular redox state or intracellular Zn(2+) signalling. Because high-frequency PP inputs to MF-primed CA3 pyramidal cells not only induce homosynaptic LTP but also restore hyperexcitability, this input-specific bidirectional regulation of intrinsic excitability may provide a cellular basis for understanding ensemble dynamics in the CA3 network. KEY POINTS: Intrinsic excitability plays a pivotal role in recruiting principal cells to neuronal memory ensembles. Mossy fibre inputs prime hippocampal CA3 pyramidal cells by enhancing their intrinsic excitability and excitatory postsynaptic potential (EPSP)-to-spike coupling at perforant path (PP) synapses. High-frequency PP inputs to such primed cells not only induce long-term potentiation of synaptic weights but also restore the high excitability state to baseline. This input-specific bidirectional regulation of intrinsic excitability may offer a cellular basis for understanding the ensemble dynamics in the hippocampal CA3 network.

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