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Cholinergic afferent stimulation induces axonal function plasticity in adult hippocampal granule cells.


ABSTRACT: Acetylcholine critically influences hippocampal-dependent learning. Cholinergic fibers innervate hippocampal neuron axons, dendrites, and somata. The effects of acetylcholine on axonal information processing, though, remain unknown. By stimulating cholinergic fibers and making electrophysiological recordings from hippocampal dentate gyrus granule cells, we show that synaptically released acetylcholine preferentially lowered the action potential threshold, enhancing intrinsic excitability and synaptic potential-spike coupling. These effects persisted for at least 30 min after the stimulation paradigm and were due to muscarinic receptor activation. This caused sustained elevation of axonal intracellular Ca(2+) via T-type Ca(2+) channels, as indicated by two-photon imaging. The enhanced Ca(2+) levels inhibited an axonal KV7/M current, decreasing the spike threshold. In support, immunohistochemistry revealed muscarinic M1 receptor, CaV3.2, and KV7.2/7.3 subunit localization in granule cell axons. Since alterations in axonal signaling affect neuronal firing patterns and neurotransmitter release, this is an unreported cellular mechanism by which acetylcholine might, at least partly, enhance cognitive processing.

SUBMITTER: Martinello K 

PROVIDER: S-EPMC4306544 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

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Cholinergic afferent stimulation induces axonal function plasticity in adult hippocampal granule cells.

Martinello Katiuscia K   Huang Zhuo Z   Lujan Rafael R   Tran Baouyen B   Watanabe Masahiko M   Cooper Edward C EC   Brown David A DA   Shah Mala M MM  

Neuron 20150108 2


Acetylcholine critically influences hippocampal-dependent learning. Cholinergic fibers innervate hippocampal neuron axons, dendrites, and somata. The effects of acetylcholine on axonal information processing, though, remain unknown. By stimulating cholinergic fibers and making electrophysiological recordings from hippocampal dentate gyrus granule cells, we show that synaptically released acetylcholine preferentially lowered the action potential threshold, enhancing intrinsic excitability and syn  ...[more]

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2024-09-04 | GSE202481 | GEO