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Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses
Our knowledge on synaptic transmission in the central nervous system has often been obtained by evoking synaptic responses to populations of synapses. Analysis of the variance in synaptic responses can be applied as a method to predict whether a change in synaptic responses is a consequence of alter...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10388551/ https://www.ncbi.nlm.nih.gov/pubmed/37528963 http://dx.doi.org/10.3389/fncel.2023.1232541 |
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author | Lumeij, Lucas B. van Huijstee, Aile N. Cappaert, Natalie L. M. Kessels, Helmut W. |
author_facet | Lumeij, Lucas B. van Huijstee, Aile N. Cappaert, Natalie L. M. Kessels, Helmut W. |
author_sort | Lumeij, Lucas B. |
collection | PubMed |
description | Our knowledge on synaptic transmission in the central nervous system has often been obtained by evoking synaptic responses to populations of synapses. Analysis of the variance in synaptic responses can be applied as a method to predict whether a change in synaptic responses is a consequence of altered presynaptic neurotransmitter release or postsynaptic receptors. However, variance analysis is based on binomial statistics, which assumes that synapses are uniform. In reality, synapses are far from uniform, which questions the reliability of variance analysis when applying this method to populations of synapses. To address this, we used an in silico model for evoked synaptic responses and compared variance analysis outcomes between populations of uniform versus non-uniform synapses. This simulation revealed that variance analysis produces similar results irrespectively of the grade of uniformity of synapses. We put this variance analysis to the test with an electrophysiology experiment using a model system for which the loci of plasticity are well established: the effect of amyloid-β on synapses. Variance analysis correctly predicted that postsynaptically produced amyloid-β triggered predominantly a loss of synapses and a minor reduction of postsynaptic currents in remaining synapses with little effect on presynaptic release probability. We propose that variance analysis can be reliably used to predict the locus of synaptic changes for populations of non-uniform synapses. |
format | Online Article Text |
id | pubmed-10388551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103885512023-08-01 Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses Lumeij, Lucas B. van Huijstee, Aile N. Cappaert, Natalie L. M. Kessels, Helmut W. Front Cell Neurosci Neuroscience Our knowledge on synaptic transmission in the central nervous system has often been obtained by evoking synaptic responses to populations of synapses. Analysis of the variance in synaptic responses can be applied as a method to predict whether a change in synaptic responses is a consequence of altered presynaptic neurotransmitter release or postsynaptic receptors. However, variance analysis is based on binomial statistics, which assumes that synapses are uniform. In reality, synapses are far from uniform, which questions the reliability of variance analysis when applying this method to populations of synapses. To address this, we used an in silico model for evoked synaptic responses and compared variance analysis outcomes between populations of uniform versus non-uniform synapses. This simulation revealed that variance analysis produces similar results irrespectively of the grade of uniformity of synapses. We put this variance analysis to the test with an electrophysiology experiment using a model system for which the loci of plasticity are well established: the effect of amyloid-β on synapses. Variance analysis correctly predicted that postsynaptically produced amyloid-β triggered predominantly a loss of synapses and a minor reduction of postsynaptic currents in remaining synapses with little effect on presynaptic release probability. We propose that variance analysis can be reliably used to predict the locus of synaptic changes for populations of non-uniform synapses. Frontiers Media S.A. 2023-07-17 /pmc/articles/PMC10388551/ /pubmed/37528963 http://dx.doi.org/10.3389/fncel.2023.1232541 Text en Copyright © 2023 Lumeij, van Huijstee, Cappaert and Kessels. 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 | Neuroscience Lumeij, Lucas B. van Huijstee, Aile N. Cappaert, Natalie L. M. Kessels, Helmut W. Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title | Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title_full | Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title_fullStr | Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title_full_unstemmed | Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title_short | Variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
title_sort | variance analysis as a method to predict the locus of plasticity at populations of non-uniform synapses |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10388551/ https://www.ncbi.nlm.nih.gov/pubmed/37528963 http://dx.doi.org/10.3389/fncel.2023.1232541 |
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