Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex

Author:

Canetta Sarah12,Teboul Eric2ORCID,Holt Emma2,Bolkan Scott S123,Padilla-Coreano Nancy145,Gordon Joshua A6,Harrison Neil L78,Kellendonk Christoph127

Affiliation:

1. Department of Psychiatry, Columbia University Medical Center, New York, NY 10032, USA

2. Division of Molecular Therapeutics, New York State Psychiatric Institute, New York, NY 10032, USA

3. Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544, USA

4. Division of Integrative Neuroscience, New York State Psychiatric Institute, New York, NY 10032, USA

5. Department of Systems Neuroscience, Salk Institute for Biological Studies, La Jolla, CA 92037, USA

6. National Institute of Mental Health, Bethesda, MD 20892, USA

7. Department of Molecular Pharmacology and Therapeutics, Columbia University Medical Center, New York, NY 10032, USA

8. Department of Anesthesiology, Columbia University Medical Center, New York, NY 10032, USA

Abstract

Abstract The medial prefrontal cortex (mPFC) integrates inputs from multiple subcortical regions including the mediodorsal nucleus of the thalamus (MD) and the ventral hippocampus (vHPC). How the mPFC differentially processes these inputs is not known. One possibility is that these two inputs target discreet populations of mPFC cells. Alternatively, individual prefrontal cells could receive convergent inputs but distinguish between both inputs based on synaptic differences, such as communication frequency. To address this, we utilized a dual wavelength optogenetic approach to stimulate MD and vHPC inputs onto single, genetically defined mPFC neuronal subtypes. Specifically, we compared the convergence and synaptic dynamics of both inputs onto mPFC pyramidal cells, and parvalbumin (PV)- and vasoactive intestinal peptide (VIP)-expressing interneurons. We found that all individual pyramidal neurons in layer 2/3 of the mPFC receive convergent input from both MD and vHPC. In contrast, PV neurons receive input biased from the MD, while VIP cells receive input biased from the vHPC. Independent of the target, MD inputs transferred information more reliably at higher frequencies (20 Hz) than vHPC inputs. Thus, MD and vHPC projections converge functionally onto mPFC pyramidal cells, but both inputs are distinguished by frequency-dependent synaptic dynamics and preferential engagement of discreet interneuron populations.

Funder

National Institute of Mental Health

Brain and Behavior Research Foundation

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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