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Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex.
Canetta, Sarah; Teboul, Eric; Holt, Emma; Bolkan, Scott S; Padilla-Coreano, Nancy; Gordon, Joshua A; Harrison, Neil L; Kellendonk, Christoph.
Afiliación
  • Canetta S; Department of Psychiatry, Columbia University Medical Center, New York, NY 10032, USA.
  • Teboul E; Division of Molecular Therapeutics, New York State Psychiatric Institute, New York, NY 10032, USA.
  • Holt E; Division of Molecular Therapeutics, New York State Psychiatric Institute, New York, NY 10032, USA.
  • Bolkan SS; Division of Molecular Therapeutics, New York State Psychiatric Institute, New York, NY 10032, USA.
  • Padilla-Coreano N; Department of Psychiatry, Columbia University Medical Center, New York, NY 10032, USA.
  • Gordon JA; Division of Molecular Therapeutics, New York State Psychiatric Institute, New York, NY 10032, USA.
  • Harrison NL; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544, USA.
  • Kellendonk C; Department of Psychiatry, Columbia University Medical Center, New York, NY 10032, USA.
Cereb Cortex Commun ; 1(1): tgaa084, 2020.
Article en En | MEDLINE | ID: mdl-33381761
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cereb Cortex Commun Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cereb Cortex Commun Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos