Author
Listed:
- Pojeong Park
(University of Bristol
Seoul National University
Mount Sinai Hospital
University of Toronto)
- John Georgiou
(Mount Sinai Hospital)
- Thomas M. Sanderson
(University of Bristol
Seoul National University
Mount Sinai Hospital)
- Kwang-Hee Ko
(Seoul National University)
- Heather Kang
(University of Bristol
Seoul National University
Mount Sinai Hospital
University of Toronto)
- Ji-il Kim
(Seoul National University)
- Clarrisa A. Bradley
(Seoul National University
The Hospital for Sick Children)
- Zuner A. Bortolotto
(University of Bristol)
- Min Zhuo
(Seoul National University
University of Toronto)
- Bong-Kiun Kaang
(Seoul National University)
- Graham L. Collingridge
(University of Bristol
Seoul National University
Mount Sinai Hospital
University of Toronto)
Abstract
Long-term potentiation (LTP) at hippocampal CA1 synapses can be expressed by an increase either in the number (N) of AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) receptors or in their single channel conductance (γ). Here, we have established how these distinct synaptic processes contribute to the expression of LTP in hippocampal slices obtained from young adult rodents. LTP induced by compressed theta burst stimulation (TBS), with a 10 s inter-episode interval, involves purely an increase in N (LTPN). In contrast, either a spaced TBS, with a 10 min inter-episode interval, or a single TBS, delivered when PKA is activated, results in LTP that is associated with a transient increase in γ (LTPγ), caused by the insertion of calcium-permeable (CP)-AMPA receptors. Activation of CaMKII is necessary and sufficient for LTPN whilst PKA is additionally required for LTPγ. Thus, two mechanistically distinct forms of LTP co-exist at these synapses.
Suggested Citation
Pojeong Park & John Georgiou & Thomas M. Sanderson & Kwang-Hee Ko & Heather Kang & Ji-il Kim & Clarrisa A. Bradley & Zuner A. Bortolotto & Min Zhuo & Bong-Kiun Kaang & Graham L. Collingridge, 2021.
"PKA drives an increase in AMPA receptor unitary conductance during LTP in the hippocampus,"
Nature Communications, Nature, vol. 12(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-020-20523-3
DOI: 10.1038/s41467-020-20523-3
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