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Modulation of Neural Networks by Interleukin-1

Interleukin-1 (IL-1) is an inflammatory cytokine that has been shown to modulate neuronal signaling in homeostasis and diseases. In homeostasis, IL-1 regulates sleep and memory formation, whereas in diseases, IL-1 impairs memory and alters affect. Interestingly, IL-1 can cause long-lasting changes i...

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Detalles Bibliográficos
Autores principales: Nemeth, Daniel P., Quan, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461735/
https://www.ncbi.nlm.nih.gov/pubmed/34631418
http://dx.doi.org/10.3233/BPL-200109
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author Nemeth, Daniel P.
Quan, Ning
author_facet Nemeth, Daniel P.
Quan, Ning
author_sort Nemeth, Daniel P.
collection PubMed
description Interleukin-1 (IL-1) is an inflammatory cytokine that has been shown to modulate neuronal signaling in homeostasis and diseases. In homeostasis, IL-1 regulates sleep and memory formation, whereas in diseases, IL-1 impairs memory and alters affect. Interestingly, IL-1 can cause long-lasting changes in behavior, suggesting IL-1 can alter neuroplasticity. The neuroplastic effects of IL-1 are mediated via its cognate receptor, Interleukin-1 Type 1 Receptor (IL-1R1), and are dependent on the distribution and cell type(s) of IL-1R1 expression. Recent reports found that IL-1R1 expression is restricted to discrete subpopulations of neurons, astrocytes, and endothelial cells and suggest IL-1 can influence neural circuits directly through neuronal IL-1R1 or indirectly via non-neuronal IL-1R1. In this review, we analyzed multiple mechanisms by which IL-1/IL-1R1 signaling might impact neuroplasticity based upon the most up-to-date literature and provided potential explanations to clarify discrepant and confusing findings reported in the past.
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spelling pubmed-84617352021-10-07 Modulation of Neural Networks by Interleukin-1 Nemeth, Daniel P. Quan, Ning Brain Plast Review Interleukin-1 (IL-1) is an inflammatory cytokine that has been shown to modulate neuronal signaling in homeostasis and diseases. In homeostasis, IL-1 regulates sleep and memory formation, whereas in diseases, IL-1 impairs memory and alters affect. Interestingly, IL-1 can cause long-lasting changes in behavior, suggesting IL-1 can alter neuroplasticity. The neuroplastic effects of IL-1 are mediated via its cognate receptor, Interleukin-1 Type 1 Receptor (IL-1R1), and are dependent on the distribution and cell type(s) of IL-1R1 expression. Recent reports found that IL-1R1 expression is restricted to discrete subpopulations of neurons, astrocytes, and endothelial cells and suggest IL-1 can influence neural circuits directly through neuronal IL-1R1 or indirectly via non-neuronal IL-1R1. In this review, we analyzed multiple mechanisms by which IL-1/IL-1R1 signaling might impact neuroplasticity based upon the most up-to-date literature and provided potential explanations to clarify discrepant and confusing findings reported in the past. IOS Press 2021-08-23 /pmc/articles/PMC8461735/ /pubmed/34631418 http://dx.doi.org/10.3233/BPL-200109 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Nemeth, Daniel P.
Quan, Ning
Modulation of Neural Networks by Interleukin-1
title Modulation of Neural Networks by Interleukin-1
title_full Modulation of Neural Networks by Interleukin-1
title_fullStr Modulation of Neural Networks by Interleukin-1
title_full_unstemmed Modulation of Neural Networks by Interleukin-1
title_short Modulation of Neural Networks by Interleukin-1
title_sort modulation of neural networks by interleukin-1
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461735/
https://www.ncbi.nlm.nih.gov/pubmed/34631418
http://dx.doi.org/10.3233/BPL-200109
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