The biophysical basis underlying the maintenance of early phase long-term potentiation.

The maintenance of synaptic changes resulting from long-term potentiation (LTP) is essential for brain function such as memory and learning. Different LTP phases have been associated with diverse molecular processes and pathways, and the molecular underpinnings of LTP on the short, as well as long t...

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Main Authors: Moritz F P Becker, Christian Tetzlaff
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-03-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1008813
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spelling doaj-ca22e2893afb4e88845992ab7773a5092021-08-05T04:32:30ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-03-01173e100881310.1371/journal.pcbi.1008813The biophysical basis underlying the maintenance of early phase long-term potentiation.Moritz F P BeckerChristian TetzlaffThe maintenance of synaptic changes resulting from long-term potentiation (LTP) is essential for brain function such as memory and learning. Different LTP phases have been associated with diverse molecular processes and pathways, and the molecular underpinnings of LTP on the short, as well as long time scales, are well established. However, the principles on the intermediate time scale of 1-6 hours that mediate the early phase of LTP (E-LTP) remain elusive. We hypothesize that the interplay between specific features of postsynaptic receptor trafficking is responsible for sustaining synaptic changes during this LTP phase. We test this hypothesis by formalizing a biophysical model that integrates several experimentally-motivated mechanisms. The model captures a wide range of experimental findings and predicts that synaptic changes are preserved for hours when the receptor dynamics are shaped by the interplay of structural changes of the spine in conjunction with increased trafficking from recycling endosomes and the cooperative binding of receptors. Furthermore, our model provides several predictions to verify our findings experimentally.https://doi.org/10.1371/journal.pcbi.1008813
collection DOAJ
language English
format Article
sources DOAJ
author Moritz F P Becker
Christian Tetzlaff
spellingShingle Moritz F P Becker
Christian Tetzlaff
The biophysical basis underlying the maintenance of early phase long-term potentiation.
PLoS Computational Biology
author_facet Moritz F P Becker
Christian Tetzlaff
author_sort Moritz F P Becker
title The biophysical basis underlying the maintenance of early phase long-term potentiation.
title_short The biophysical basis underlying the maintenance of early phase long-term potentiation.
title_full The biophysical basis underlying the maintenance of early phase long-term potentiation.
title_fullStr The biophysical basis underlying the maintenance of early phase long-term potentiation.
title_full_unstemmed The biophysical basis underlying the maintenance of early phase long-term potentiation.
title_sort biophysical basis underlying the maintenance of early phase long-term potentiation.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2021-03-01
description The maintenance of synaptic changes resulting from long-term potentiation (LTP) is essential for brain function such as memory and learning. Different LTP phases have been associated with diverse molecular processes and pathways, and the molecular underpinnings of LTP on the short, as well as long time scales, are well established. However, the principles on the intermediate time scale of 1-6 hours that mediate the early phase of LTP (E-LTP) remain elusive. We hypothesize that the interplay between specific features of postsynaptic receptor trafficking is responsible for sustaining synaptic changes during this LTP phase. We test this hypothesis by formalizing a biophysical model that integrates several experimentally-motivated mechanisms. The model captures a wide range of experimental findings and predicts that synaptic changes are preserved for hours when the receptor dynamics are shaped by the interplay of structural changes of the spine in conjunction with increased trafficking from recycling endosomes and the cooperative binding of receptors. Furthermore, our model provides several predictions to verify our findings experimentally.
url https://doi.org/10.1371/journal.pcbi.1008813
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