Optogenetic activation of dopamine D1 receptors in island cells of medial entorhinal cortex inhibits temporal association learning.
Dopamine D1 receptor
Hippocampus
Island cells
Medial entorhinal cortex
Optogenetics
Trace fear conditioning
c-Fos
Journal
Molecular brain
ISSN: 1756-6606
Titre abrégé: Mol Brain
Pays: England
ID NLM: 101468876
Informations de publication
Date de publication:
14 Nov 2023
14 Nov 2023
Historique:
received:
03
10
2023
accepted:
25
10
2023
medline:
16
11
2023
pubmed:
15
11
2023
entrez:
15
11
2023
Statut:
epublish
Résumé
A critical feature of episodic memory formation is to associate temporally segregated events as an episode, called temporal association learning. The medial entorhinal cortical-hippocampal (EC-HPC) networks is essential for temporal association learning. We have previously demonstrated that pyramidal cells in the medial EC (MEC) layer III project to the hippocampal CA1 pyramidal cells and are necessary for trace fear conditioning (TFC), which is an associative learning between tone and aversive shock with the temporal gap. On the other hand, Island cells in MECII, project to GABAergic neurons in hippocampal CA1, suppress the MECIII input into the CA1 pyramidal cells through the feed-forward inhibition, and inhibit TFC. However, it remains unknown about how Island cells activity is regulated during TFC. In this study, we report that dopamine D1 receptor is preferentially expressed in Island cells in the MEC. Optogenetic activation of dopamine D1 receptors in Island cells facilitate the Island cell activity and inhibited hippocampal CA1 pyramidal cell activity during TFC. The optogenetic activation caused the impairment of TFC memory recall without affecting contextual fear memory recall. These results suggest that dopamine D1 receptor in Island cells have a crucial role for the regulation of temporal association learning.
Identifiants
pubmed: 37964372
doi: 10.1186/s13041-023-01065-3
pii: 10.1186/s13041-023-01065-3
pmc: PMC10647136
doi:
Substances chimiques
Receptors, Dopamine D1
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
78Subventions
Organisme : NIMH NIH HHS
ID : R01 MH120134
Pays : United States
Organisme : NIMH NIH HHS
ID : R01MH120134
Pays : United States
Informations de copyright
© 2023. The Author(s).
Références
Nat Neurosci. 2010 Jul;13(7):822-4
pubmed: 20512133
Cell. 2014 Jun 19;157(7):1535-51
pubmed: 24949967
Nat Rev Neurosci. 2004 Jun;5(6):483-94
pubmed: 15152198
Learn Mem. 2021 Aug 16;28(9):319-328
pubmed: 34400533
Nature. 2021 Oct;598(7880):321-326
pubmed: 34552245
Neuroscience. 2014 Jan 31;258:74-83
pubmed: 24220689
J Neurochem. 2023 Jul;166(2):172-188
pubmed: 37248771
Annu Rev Neurosci. 2001;24:897-931
pubmed: 11520922
Neuron. 2015 Sep 23;87(6):1317-1331
pubmed: 26402611
Proc Natl Acad Sci U S A. 2014 Jun 3;111(22):8245-50
pubmed: 24843151
Prog Neurobiol. 2004 Dec;74(5):301-20
pubmed: 15582224
Trends Neurosci. 1998 Aug;21(8):317-23
pubmed: 9720595
Cereb Cortex. 1993 Nov-Dec;3(6):533-50
pubmed: 7907902
Sci Rep. 2015 Dec 10;5:17461
pubmed: 26658842
Science. 2014 Feb 21;343(6173):896-901
pubmed: 24457215