|Title||Dendritic inhibition provided by interneuron-specific cells controls the firing rate and timing of the hippocampal feedback inhibitory circuitry.|
|Publication Type||Journal Article|
|Year of Publication||2014|
|Authors||Tyan, L, Chamberland, S, Magnin, E, Camiré, O, Francavilla, R, David, LSuzanne, Deisseroth, K, Topolnik, L|
|Date Published||2014 Mar 26|
|Keywords||Action Potentials, Animals, Animals, Newborn, Dendrites, Female, GABA Antagonists, Green Fluorescent Proteins, Hippocampus, In Vitro Techniques, Inhibitory Postsynaptic Potentials, Interneurons, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Nerve Net, Neural Inhibition, Pyridazines, Time Factors, Vasoactive Intestinal Peptide|
In cortical networks, different types of inhibitory interneurons control the activity of glutamatergic principal cells and GABAergic interneurons. Principal neurons represent the major postsynaptic target of most interneurons; however, a population of interneurons that is dedicated to the selective innervation of GABAergic cells exists in the CA1 area of the hippocampus. The physiological properties of these cells and their functional relevance for network computations remain unknown. Here, we used a combination of dual simultaneous patch-clamp recordings and targeted optogenetic stimulation in acute mouse hippocampal slices to examine how one class of interneuron-specific (IS) cells controls the activity of its GABAergic targets. We found that type 3 IS (IS3) cells that coexpress the vasoactive intestinal polypeptide (VIP) and calretinin contact several distinct types of interneurons within the hippocampal CA1 stratum oriens/alveus (O/A), with preferential innervation of oriens-lacunosum moleculare cells (OLMs) through dendritic synapses. In contrast, VIP-positive basket cells provided perisomatic inhibition to CA1 pyramidal neurons with the asynchronous GABA release and were not connected with O/A interneurons. Furthermore, unitary IPSCs recorded at IS3-OLM synapses had a small amplitude and low release probability but summated efficiently during high-frequency firing of IS3 interneurons. Moreover, the synchronous generation of a single spike in several IS cells that converged onto a single OLM controlled the firing rate and timing of OLM interneurons. Therefore, dendritic inhibition originating from IS cells is needed for the flexible activity-dependent recruitment of OLM interneurons for feedback inhibition.
|Alternate Journal||J. Neurosci.|