Further evidence that CP-AMPARs are critically involved in synaptic tag and capture at hippocampal CA1 synapses.


Journal

Molecular brain
ISSN: 1756-6606
Titre abrégé: Mol Brain
Pays: England
ID NLM: 101468876

Informations de publication

Date de publication:
01 02 2021
Historique:
received: 01 12 2020
accepted: 16 01 2021
entrez: 2 2 2021
pubmed: 3 2 2021
medline: 5 11 2021
Statut: epublish

Résumé

The synaptic tag and capture (STC) hypothesis provides an important theoretical basis for understanding the synaptic basis of associative learning. We recently provided pharmacological evidence that calcium-permeable AMPA receptors (CP-AMPARs) are a crucial component of this form of heterosynaptic metaplasticity. Here we have investigated two predictions that arise on the basis of CP-AMPARs serving as a trigger of STC. Firstly, we compared the effects of the order in which we delivered a strong theta burst stimulation (TBS) protocol (75 pulses) and a weak TBS protocol (15 pulses) to two independent inputs. We only observed significant heterosynaptic metaplasticity when the strong TBS preceded the weak TBS. Second, we found that pausing stimulation following either the sTBS or the wTBS for ~20 min largely eliminates the heterosynaptic metaplasticity. These observations are consistent with a process that is triggered by the synaptic insertion of CP-AMPARs and provide a framework for establishing the underlying molecular mechanisms.

Identifiants

pubmed: 33526063
doi: 10.1186/s13041-021-00737-2
pii: 10.1186/s13041-021-00737-2
pmc: PMC7851922
doi:

Substances chimiques

Receptors, AMPA 0
Calcium SY7Q814VUP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

26

Subventions

Organisme : CIHR
ID : 66975
Pays : Canada
Organisme : CIHR
ID : FDN154276
Pays : Canada
Organisme : CIHR
ID : 84256
Pays : Canada

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Auteurs

Pojeong Park (P)

School of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, Korea.
Department of Physiology, Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.
Glutamate Receptor Group, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol, BS1 3NY, UK.

Heather Kang (H)

Department of Physiology, Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.
Glutamate Receptor Group, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol, BS1 3NY, UK.

John Georgiou (J)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.

Min Zhuo (M)

School of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, Korea.
Department of Physiology, Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.

Bong-Kiun Kaang (BK)

School of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, Korea.

Graham L Collingridge (GL)

School of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, Korea. collingridge@lunenfeld.ca.
Department of Physiology, Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada. collingridge@lunenfeld.ca.
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada. collingridge@lunenfeld.ca.
Glutamate Receptor Group, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol, BS1 3NY, UK. collingridge@lunenfeld.ca.
TANZ Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, M5S 1A8, Canada. collingridge@lunenfeld.ca.

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