| Literature DB >> 26965902 |
Michele Ferrante1,2, Christopher F Shay1,2,3, Yusuke Tsuno1,2, G William Chapman1, Michael E Hasselmo1,2,3,4.
Abstract
Medial entorhinal cortex Layer-II stellate cells (mEC-LII-SCs) primarily interact via inhibitory interneurons. This suggests the presence of alternative mechanisms other than excitatory synaptic inputs for triggering action potentials (APs) in stellate cells during spatial navigation. Our intracellular recordings show that the hyperpolarization-activated cation current (Ih) allows post-inhibitory-rebound spikes (PIRS) in mEC-LII-SCs. In vivo, strong inhibitory-post-synaptic potentials immediately preceded most APs shortening their delay and enhancing excitability. In vitro experiments showed that inhibition initiated spikes more effectively than excitation and that more dorsal mEC-LII-SCs produced faster and more synchronous spikes. In contrast, PIRS in Layer-II/III pyramidal cells were harder to evoke, voltage-independent, and slower in dorsal mEC. In computational simulations, mEC-LII-SCs morphology and Ih homeostatically regulated the dorso-ventral differences in PIRS timing and most dendrites generated PIRS with a narrow range of stimulus amplitudes. These results suggest inhibitory inputs could mediate the emergence of grid cell firing in a neuronal network.Entities:
Keywords: entorhinal cortex; hyperpolarization-activated cation current (Ih); inhibition; post-inhibitory spikes; stellate cells
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Year: 2017 PMID: 26965902 PMCID: PMC5963826 DOI: 10.1093/cercor/bhw058
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357