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Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram
The engram encoding the interval between the conditional stimulus (CS) and the unconditional stimulus (US) in eyeblink conditioning resides within a small population of cerebellar Purkinje cells. CSs activate this engram to produce a pause in the spontaneous firing rate of the cell, which times the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669310/ https://www.ncbi.nlm.nih.gov/pubmed/36405788 http://dx.doi.org/10.3389/fncom.2022.1019812 |
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author | Gallistel, Charles Randy Johansson, Fredrik Jirenhed, Dan-Anders Rasmussen, Anders Ricci, Matthew Hesslow, Germund |
author_facet | Gallistel, Charles Randy Johansson, Fredrik Jirenhed, Dan-Anders Rasmussen, Anders Ricci, Matthew Hesslow, Germund |
author_sort | Gallistel, Charles Randy |
collection | PubMed |
description | The engram encoding the interval between the conditional stimulus (CS) and the unconditional stimulus (US) in eyeblink conditioning resides within a small population of cerebellar Purkinje cells. CSs activate this engram to produce a pause in the spontaneous firing rate of the cell, which times the CS-conditional blink. We developed a Bayesian algorithm that finds pause onsets and offsets in the records from individual CS-alone trials. We find that the pause consists of a single unusually long interspike interval. Its onset and offset latencies and their trial-to-trial variability are proportional to the CS-US interval. The coefficient of variation (CoV = σ/μ) are comparable to the CoVs for the conditional eye blink. The average trial-to-trial correlation between the onset latencies and the offset latencies is close to 0, implying that the onsets and offsets are mediated by two stochastically independent readings of the engram. The onset of the pause is step-like; there is no decline in firing rate between the onset of the CS and the onset of the pause. A single presynaptic spike volley suffices to trigger the reading of the engram; and the pause parameters are unaffected by subsequent volleys. The Fano factors for trial-to-trial variations in the distribution of interspike intervals within the intertrial intervals indicate pronounced non-stationarity in the endogenous spontaneous spiking rate, on which the CS-triggered firing pause supervenes. These properties of the spontaneous firing and of the engram read out may prove useful in finding the cell-intrinsic, molecular-level structure that encodes the CS-US interval. |
format | Online Article Text |
id | pubmed-9669310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96693102022-11-18 Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram Gallistel, Charles Randy Johansson, Fredrik Jirenhed, Dan-Anders Rasmussen, Anders Ricci, Matthew Hesslow, Germund Front Comput Neurosci Computational Neuroscience The engram encoding the interval between the conditional stimulus (CS) and the unconditional stimulus (US) in eyeblink conditioning resides within a small population of cerebellar Purkinje cells. CSs activate this engram to produce a pause in the spontaneous firing rate of the cell, which times the CS-conditional blink. We developed a Bayesian algorithm that finds pause onsets and offsets in the records from individual CS-alone trials. We find that the pause consists of a single unusually long interspike interval. Its onset and offset latencies and their trial-to-trial variability are proportional to the CS-US interval. The coefficient of variation (CoV = σ/μ) are comparable to the CoVs for the conditional eye blink. The average trial-to-trial correlation between the onset latencies and the offset latencies is close to 0, implying that the onsets and offsets are mediated by two stochastically independent readings of the engram. The onset of the pause is step-like; there is no decline in firing rate between the onset of the CS and the onset of the pause. A single presynaptic spike volley suffices to trigger the reading of the engram; and the pause parameters are unaffected by subsequent volleys. The Fano factors for trial-to-trial variations in the distribution of interspike intervals within the intertrial intervals indicate pronounced non-stationarity in the endogenous spontaneous spiking rate, on which the CS-triggered firing pause supervenes. These properties of the spontaneous firing and of the engram read out may prove useful in finding the cell-intrinsic, molecular-level structure that encodes the CS-US interval. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9669310/ /pubmed/36405788 http://dx.doi.org/10.3389/fncom.2022.1019812 Text en Copyright © 2022 Gallistel, Johansson, Jirenhed, Rasmussen, Ricci and Hesslow. 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 | Computational Neuroscience Gallistel, Charles Randy Johansson, Fredrik Jirenhed, Dan-Anders Rasmussen, Anders Ricci, Matthew Hesslow, Germund Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title | Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title_full | Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title_fullStr | Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title_full_unstemmed | Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title_short | Quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
title_sort | quantitative properties of the creation and activation of a cell-intrinsic duration-encoding engram |
topic | Computational Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669310/ https://www.ncbi.nlm.nih.gov/pubmed/36405788 http://dx.doi.org/10.3389/fncom.2022.1019812 |
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