Excitatory neurons in stratum radiatum provide an alternative pathway for excitation flow that escapes perisomatic inhibition

Author:

Lebedeva Julia12,Jappy David34,Nasretdinov Azat1,Vazetdinova Alina13,Krut Viktoria3,Sokolov Rostislav45,Dobryakova Yulia36,Eliava Marina2,Grinevich Valery2,Rozov Andrei137ORCID

Affiliation:

1. OpenLab of Neurobiology, Kazan Federal University

2. Department of Neuropeptide Research in Psychiatry, Central Institute of Mental Health, University of Heidelberg

3. Federal Center of Brain Research and Neurotechnologies

4. Institute of Neuroscience, Lobachevsky State University of Nizhniy Novgorod

5. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences

6. Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences

7. Department of Physiology and Pathophysiology, Heidelberg University

Abstract

For over half a century, it has been postulated that the internal excitatory circuit in the hippocampus consists of three relay stations. Excitation arrives from the entorhinal cortex to the DG granule cells, is transmitted through the mossy fibers to CA3 pyramidal cells, and is then transmitted through Schaffer collaterals to CA1 pyramidal neurons. In all three structures (DG, CA3 and CA1), the activity of the excitatory neurons involved in the synaptic transmission of excitation are under the control of inhibitory basket neurons that are recruited into network activity via feed-forward and feed-back excitation. However, in the late 90s “stratum radiatum giant cells” were described as a novel type of neuron with the anatomical features of excitatory cells. Since then, the role of these cells in the hippocampal circuitry has not been well understood. Here, using optogenetic and electrophysiological techniques we characterized the functional location of these neurons within the hippocampal network. We show that: (i) the main excitatory drive to giant excitatory neurons in stratum radiatum (ExN R ) comes via Schaffer collaterals; (ii) within the CA1 field, ExN R are not directly connected with local pyramidal cells, but provide massive and efficient excitatory input to parvalbumin positive (PV+) interneurons; (iii) ExN R are reciprocally innervated by bistratified cells, but not inhibited by backet interneurons; (iv) the efficiency of ExN R excitation to PV+ interneurons is sufficient for a single ExN R action potential to trigger massive inhibition of downstream CA1 pyramidal cells. Taken together, our data shows that ExN R constitute an alternative pathway of excitation for CA1 interneurons that avoids the burden of perisomatic inhibition.

Publisher

eLife Sciences Publications, Ltd

Reference27 articles.

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