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Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD

In area CA1 of the hippocampus, long-term depression (LTD) can be induced by activating group I metabotropic glutamate receptors (mGluRs), with the selective agonist DHPG. There is evidence that mGluR-LTD can be expressed by either a decrease in the probability of neurotransmitter release [P(r)] or...

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Autores principales: Sanderson, Thomas M., Ralph, Liam T., Amici, Mascia, Ng, Ai Na, Kaang, Bong-Kiun, Zhuo, Min, Kim, Sang Jeong, Georgiou, John, Collingridge, Graham L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126322/
https://www.ncbi.nlm.nih.gov/pubmed/35615440
http://dx.doi.org/10.3389/fnsyn.2022.857675
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author Sanderson, Thomas M.
Ralph, Liam T.
Amici, Mascia
Ng, Ai Na
Kaang, Bong-Kiun
Zhuo, Min
Kim, Sang Jeong
Georgiou, John
Collingridge, Graham L.
author_facet Sanderson, Thomas M.
Ralph, Liam T.
Amici, Mascia
Ng, Ai Na
Kaang, Bong-Kiun
Zhuo, Min
Kim, Sang Jeong
Georgiou, John
Collingridge, Graham L.
author_sort Sanderson, Thomas M.
collection PubMed
description In area CA1 of the hippocampus, long-term depression (LTD) can be induced by activating group I metabotropic glutamate receptors (mGluRs), with the selective agonist DHPG. There is evidence that mGluR-LTD can be expressed by either a decrease in the probability of neurotransmitter release [P(r)] or by a change in postsynaptic AMPA receptor number. However, what determines the locus of expression is unknown. We investigated the expression mechanisms of mGluR-LTD using either a low (30 μM) or a high (100 μM) concentration of (RS)-DHPG. We found that 30 μM DHPG generated presynaptic LTD that required the co-activation of NMDA receptors, whereas 100 μM DHPG resulted in postsynaptic LTD that was independent of the activation of NMDA receptors. We found that both forms of LTD occur at the same synapses and that these may constitute the population with the lowest basal P(r). Our results reveal an unexpected complexity to mGluR-mediated synaptic plasticity in the hippocampus.
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spelling pubmed-91263222022-05-24 Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD Sanderson, Thomas M. Ralph, Liam T. Amici, Mascia Ng, Ai Na Kaang, Bong-Kiun Zhuo, Min Kim, Sang Jeong Georgiou, John Collingridge, Graham L. Front Synaptic Neurosci Synaptic Neuroscience In area CA1 of the hippocampus, long-term depression (LTD) can be induced by activating group I metabotropic glutamate receptors (mGluRs), with the selective agonist DHPG. There is evidence that mGluR-LTD can be expressed by either a decrease in the probability of neurotransmitter release [P(r)] or by a change in postsynaptic AMPA receptor number. However, what determines the locus of expression is unknown. We investigated the expression mechanisms of mGluR-LTD using either a low (30 μM) or a high (100 μM) concentration of (RS)-DHPG. We found that 30 μM DHPG generated presynaptic LTD that required the co-activation of NMDA receptors, whereas 100 μM DHPG resulted in postsynaptic LTD that was independent of the activation of NMDA receptors. We found that both forms of LTD occur at the same synapses and that these may constitute the population with the lowest basal P(r). Our results reveal an unexpected complexity to mGluR-mediated synaptic plasticity in the hippocampus. Frontiers Media S.A. 2022-05-09 /pmc/articles/PMC9126322/ /pubmed/35615440 http://dx.doi.org/10.3389/fnsyn.2022.857675 Text en Copyright © 2022 Sanderson, Ralph, Amici, Ng, Kaang, Zhuo, Kim, Georgiou and Collingridge. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Synaptic Neuroscience
Sanderson, Thomas M.
Ralph, Liam T.
Amici, Mascia
Ng, Ai Na
Kaang, Bong-Kiun
Zhuo, Min
Kim, Sang Jeong
Georgiou, John
Collingridge, Graham L.
Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title_full Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title_fullStr Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title_full_unstemmed Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title_short Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD
title_sort selective recruitment of presynaptic and postsynaptic forms of mglur-ltd
topic Synaptic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126322/
https://www.ncbi.nlm.nih.gov/pubmed/35615440
http://dx.doi.org/10.3389/fnsyn.2022.857675
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