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Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus
Information coding in the hippocampus relies on the interplay between various neuronal ensembles. We discovered that the application of a cholinergic agonist, carbachol (Cch), which triggers oscillatory activity in the gamma range, induces the activity of matrix metalloproteinase 9 (MMP-9)—an enzyme...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258443/ https://www.ncbi.nlm.nih.gov/pubmed/33739386 http://dx.doi.org/10.1093/cercor/bhab050 |
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author | Salamian, Ahmad Legutko, Diana Nowicka, Klaudia Badyra, Bogna Kaźmierska-Grębowska, Paulina Caban, Bartosz Kowalczyk, Tomasz Kaczmarek, Leszek Beroun, Anna |
author_facet | Salamian, Ahmad Legutko, Diana Nowicka, Klaudia Badyra, Bogna Kaźmierska-Grębowska, Paulina Caban, Bartosz Kowalczyk, Tomasz Kaczmarek, Leszek Beroun, Anna |
author_sort | Salamian, Ahmad |
collection | PubMed |
description | Information coding in the hippocampus relies on the interplay between various neuronal ensembles. We discovered that the application of a cholinergic agonist, carbachol (Cch), which triggers oscillatory activity in the gamma range, induces the activity of matrix metalloproteinase 9 (MMP-9)—an enzyme necessary for the maintenance of synaptic plasticity. Using electrophysiological recordings in hippocampal organotypic slices, we show that Cch potentiates the frequency of miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs, respectively) in CA1 neurons and this effect is MMP-9 dependent. Interestingly, though MMP-9 inhibition prevents the potentiation of inhibitory events, it further boosts the frequency of excitatory mEPSCs. Such enhancement of the frequency of excitatory events is a result of increased synaptogenesis onto CA1 neurons. Thus, the function of MMP-9 in cholinergically induced plasticity in the hippocampus is to maintain the fine-tuned balance between the excitatory and the inhibitory synaptic transmission. |
format | Online Article Text |
id | pubmed-8258443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82584432021-07-07 Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus Salamian, Ahmad Legutko, Diana Nowicka, Klaudia Badyra, Bogna Kaźmierska-Grębowska, Paulina Caban, Bartosz Kowalczyk, Tomasz Kaczmarek, Leszek Beroun, Anna Cereb Cortex Original Article Information coding in the hippocampus relies on the interplay between various neuronal ensembles. We discovered that the application of a cholinergic agonist, carbachol (Cch), which triggers oscillatory activity in the gamma range, induces the activity of matrix metalloproteinase 9 (MMP-9)—an enzyme necessary for the maintenance of synaptic plasticity. Using electrophysiological recordings in hippocampal organotypic slices, we show that Cch potentiates the frequency of miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs, respectively) in CA1 neurons and this effect is MMP-9 dependent. Interestingly, though MMP-9 inhibition prevents the potentiation of inhibitory events, it further boosts the frequency of excitatory mEPSCs. Such enhancement of the frequency of excitatory events is a result of increased synaptogenesis onto CA1 neurons. Thus, the function of MMP-9 in cholinergically induced plasticity in the hippocampus is to maintain the fine-tuned balance between the excitatory and the inhibitory synaptic transmission. Oxford University Press 2021-03-19 /pmc/articles/PMC8258443/ /pubmed/33739386 http://dx.doi.org/10.1093/cercor/bhab050 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Salamian, Ahmad Legutko, Diana Nowicka, Klaudia Badyra, Bogna Kaźmierska-Grębowska, Paulina Caban, Bartosz Kowalczyk, Tomasz Kaczmarek, Leszek Beroun, Anna Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title | Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title_full | Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title_fullStr | Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title_full_unstemmed | Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title_short | Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus |
title_sort | inhibition of matrix metalloproteinase 9 activity promotes synaptogenesis in the hippocampus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258443/ https://www.ncbi.nlm.nih.gov/pubmed/33739386 http://dx.doi.org/10.1093/cercor/bhab050 |
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