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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Online Access: | https://doi.org/10.1371/journal.pcbi.1008813 |
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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 |
work_keys_str_mv |
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