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NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus

Experience-dependent expression of immediate-early gene transcription factors (IEG-TFs) can transiently change the transcriptome of active neurons and initiate persistent changes in cellular function. However, the impact of IEG-TFs on circuit connectivity and function is poorly understood. We invest...

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Autores principales: Hartzell, Andrea L, Martyniuk, Kelly M, Brigidi, G Stefano, Heinz, Daniel A, Djaja, Nathalie A, Payne, Anja, Bloodgood, Brenda L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105310/
https://www.ncbi.nlm.nih.gov/pubmed/30052197
http://dx.doi.org/10.7554/eLife.35927
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author Hartzell, Andrea L
Martyniuk, Kelly M
Brigidi, G Stefano
Heinz, Daniel A
Djaja, Nathalie A
Payne, Anja
Bloodgood, Brenda L
author_facet Hartzell, Andrea L
Martyniuk, Kelly M
Brigidi, G Stefano
Heinz, Daniel A
Djaja, Nathalie A
Payne, Anja
Bloodgood, Brenda L
author_sort Hartzell, Andrea L
collection PubMed
description Experience-dependent expression of immediate-early gene transcription factors (IEG-TFs) can transiently change the transcriptome of active neurons and initiate persistent changes in cellular function. However, the impact of IEG-TFs on circuit connectivity and function is poorly understood. We investigate the specificity with which the IEG-TF NPAS4 governs experience-dependent changes in inhibitory synaptic input onto CA1 pyramidal neurons (PNs). We show that novel sensory experience selectively enhances somatic inhibition mediated by cholecystokinin-expressing basket cells (CCKBCs) in an NPAS4-dependent manner. NPAS4 specifically increases the number of synapses made onto PNs by individual CCKBCs without altering synaptic properties. Additionally, we find that sensory experience-driven NPAS4 expression enhances depolarization-induced suppression of inhibition (DSI), a short-term form of cannabinoid-mediated plasticity expressed at CCKBC synapses. Our results indicate that CCKBC inputs are a major target of the NPAS4-dependent transcriptional program in PNs and that NPAS4 is an important regulator of plasticity mediated by endogenous cannabinoids.
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spelling pubmed-61053102018-08-23 NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus Hartzell, Andrea L Martyniuk, Kelly M Brigidi, G Stefano Heinz, Daniel A Djaja, Nathalie A Payne, Anja Bloodgood, Brenda L eLife Neuroscience Experience-dependent expression of immediate-early gene transcription factors (IEG-TFs) can transiently change the transcriptome of active neurons and initiate persistent changes in cellular function. However, the impact of IEG-TFs on circuit connectivity and function is poorly understood. We investigate the specificity with which the IEG-TF NPAS4 governs experience-dependent changes in inhibitory synaptic input onto CA1 pyramidal neurons (PNs). We show that novel sensory experience selectively enhances somatic inhibition mediated by cholecystokinin-expressing basket cells (CCKBCs) in an NPAS4-dependent manner. NPAS4 specifically increases the number of synapses made onto PNs by individual CCKBCs without altering synaptic properties. Additionally, we find that sensory experience-driven NPAS4 expression enhances depolarization-induced suppression of inhibition (DSI), a short-term form of cannabinoid-mediated plasticity expressed at CCKBC synapses. Our results indicate that CCKBC inputs are a major target of the NPAS4-dependent transcriptional program in PNs and that NPAS4 is an important regulator of plasticity mediated by endogenous cannabinoids. eLife Sciences Publications, Ltd 2018-07-27 /pmc/articles/PMC6105310/ /pubmed/30052197 http://dx.doi.org/10.7554/eLife.35927 Text en © 2018, Hartzell et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Hartzell, Andrea L
Martyniuk, Kelly M
Brigidi, G Stefano
Heinz, Daniel A
Djaja, Nathalie A
Payne, Anja
Bloodgood, Brenda L
NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title_full NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title_fullStr NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title_full_unstemmed NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title_short NPAS4 recruits CCK basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
title_sort npas4 recruits cck basket cell synapses and enhances cannabinoid-sensitive inhibition in the mouse hippocampus
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105310/
https://www.ncbi.nlm.nih.gov/pubmed/30052197
http://dx.doi.org/10.7554/eLife.35927
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