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Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory

Recent work by Ciernia et al. (2020) identified how genetic and epigenetic mechanisms interact to regulate innate immune memory in bone marrow derived macrophages. The authors examined the BTBR strain, a naturally occurring mouse model of Autism Spectrum Disorder (ASD) that captures the complex gene...

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Autores principales: Kim, Jennifer, Ciernia, Annie Vogel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294664/
https://www.ncbi.nlm.nih.gov/pubmed/34295572
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author Kim, Jennifer
Ciernia, Annie Vogel
author_facet Kim, Jennifer
Ciernia, Annie Vogel
author_sort Kim, Jennifer
collection PubMed
description Recent work by Ciernia et al. (2020) identified how genetic and epigenetic mechanisms interact to regulate innate immune memory in bone marrow derived macrophages. The authors examined the BTBR strain, a naturally occurring mouse model of Autism Spectrum Disorder (ASD) that captures the complex genetics, behavioral and immune dysregulation found in the human disorder. Immune cell cultures from the BTBR strain compared to the standard C57 showed hyper-responsive immune gene expression that was linked to altered chromatin accessibility at sites with genetic differences between the strains. Together, findings from this work demonstrated that multiple levels of gene regulation likely dictate the formation of innate immune memory and are likely disrupted in immune cells in ASD. Future work will be needed to extend these findings to immune gene regulation in the brain and how changes in immune function are related to abnormal behaviors in brain disorders.
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spelling pubmed-82946642021-07-21 Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory Kim, Jennifer Ciernia, Annie Vogel J Clin Cell Immunol Article Recent work by Ciernia et al. (2020) identified how genetic and epigenetic mechanisms interact to regulate innate immune memory in bone marrow derived macrophages. The authors examined the BTBR strain, a naturally occurring mouse model of Autism Spectrum Disorder (ASD) that captures the complex genetics, behavioral and immune dysregulation found in the human disorder. Immune cell cultures from the BTBR strain compared to the standard C57 showed hyper-responsive immune gene expression that was linked to altered chromatin accessibility at sites with genetic differences between the strains. Together, findings from this work demonstrated that multiple levels of gene regulation likely dictate the formation of innate immune memory and are likely disrupted in immune cells in ASD. Future work will be needed to extend these findings to immune gene regulation in the brain and how changes in immune function are related to abnormal behaviors in brain disorders. 2020 2020-07-28 /pmc/articles/PMC8294664/ /pubmed/34295572 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Kim, Jennifer
Ciernia, Annie Vogel
Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title_full Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title_fullStr Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title_full_unstemmed Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title_short Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory
title_sort chromatin dynamics and genetic variation combine to regulate innate immune memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294664/
https://www.ncbi.nlm.nih.gov/pubmed/34295572
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