Regulation of interneuron excitability by gap junction coupling with principal cells

Pierre F. Apostolides, Laurence O. Trussell

Research output: Contribution to journalArticle

25 Scopus citations

Abstract

Electrical coupling of inhibitory interneurons can synchronize activity across multiple neurons, thereby enhancing the reliability of inhibition onto principal cell targets. It is unclear whether downstream activity in principal cells controls the excitability of such inhibitory networks. Using paired patch-clamp recordings, we show that excitatory projection neurons (fusiform cells) and inhibitory stellate interneurons of the dorsal cochlear nucleus form an electrically coupled network through gap junctions containing connexin36 (Cxc36, also called Gjd2). Remarkably, stellate cells were more strongly coupled to fusiform cells than to other stellate cells. This heterologous coupling was functionally asymmetric, biasing electrical transmission from the principal cell to the interneuron. Optogenetically activated populations of fusiform cells reliably enhanced interneuron excitability and generated GABAergic inhibition onto the postsynaptic targets of stellate cells, whereas deep afterhyperpolarizations following fusiform cell spike trains potently inhibited stellate cells over several hundred milliseconds. Thus, the excitability of an interneuron network is bidirectionally controlled by distinct epochs of activity in principal cells.

Original languageEnglish (US)
Pages (from-to)1764-1772
Number of pages9
JournalNature Neuroscience
Volume16
Issue number12
DOIs
StatePublished - Nov 6 2013

ASJC Scopus subject areas

  • Neuroscience(all)

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