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Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review
Mild traumatic brain injuries (mTBIs) are a prevalent form of injury that can result in persistent neurological impairments. Microglial activation has become increasingly recognized as a key process regulating the pathology of white matter in a wide range of brain injury and disease contexts. As whi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684664/ https://www.ncbi.nlm.nih.gov/pubmed/34924026 http://dx.doi.org/10.1186/s40478-021-01297-1 |
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author | Velayudhan, Prashanth S. Schwab, Nicole Hazrati, Lili-Naz Wheeler, Anne L. |
author_facet | Velayudhan, Prashanth S. Schwab, Nicole Hazrati, Lili-Naz Wheeler, Anne L. |
author_sort | Velayudhan, Prashanth S. |
collection | PubMed |
description | Mild traumatic brain injuries (mTBIs) are a prevalent form of injury that can result in persistent neurological impairments. Microglial activation has become increasingly recognized as a key process regulating the pathology of white matter in a wide range of brain injury and disease contexts. As white matter damage is known to be a major contributor to the impairments that follow mTBI, microglia have rightfully become a common target of investigation for the development of mTBI therapies and biomarkers. Recent work has demonstrated that the efficacy of microglial manipulation as a therapeutic intervention following injury or disease is highly time-sensitive, emphasizing the importance of advancing our understanding of the dynamics of post-mTBI microglial activation from onset to resolution. Current reporting of microglial activation in experimental studies of mTBI is non-standardized, which has limited our ability to identify concrete patterns of post-mTBI microglial activation over time. In this review, we examine preclinical studies of mTBI that report on microglial activation in white matter regions to summarize our current understanding of these patterns. Specifically, we summarize timecourses of post-mTBI microglial activation in white matter regions of the brain, identify factors that influence this activation, examine the temporal relationship between microglial activation and other post-mTBI assessments, and compare the relative sensitivities of various methods for detecting microglial activation. While the lack of replicated experimental conditions has limited the extent of conclusions that can confidently be drawn, we find that microglia are activated over a wide range of timecourses following mTBI and that microglial activation is a long-lasting outcome of mTBI that may resolve after most typical post-mTBI assessments, with the exception of those measuring oligodendrocyte lineage cell integrity. We identify several understudied parameters of post-mTBI microglial activation in white matter, such as the inclusion of female subjects. This review summarizes our current understanding of the progression of microglial activation in white matter structures following experimental mTBI and offers suggestions for important future research directions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01297-1. |
format | Online Article Text |
id | pubmed-8684664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86846642021-12-20 Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review Velayudhan, Prashanth S. Schwab, Nicole Hazrati, Lili-Naz Wheeler, Anne L. Acta Neuropathol Commun Review Mild traumatic brain injuries (mTBIs) are a prevalent form of injury that can result in persistent neurological impairments. Microglial activation has become increasingly recognized as a key process regulating the pathology of white matter in a wide range of brain injury and disease contexts. As white matter damage is known to be a major contributor to the impairments that follow mTBI, microglia have rightfully become a common target of investigation for the development of mTBI therapies and biomarkers. Recent work has demonstrated that the efficacy of microglial manipulation as a therapeutic intervention following injury or disease is highly time-sensitive, emphasizing the importance of advancing our understanding of the dynamics of post-mTBI microglial activation from onset to resolution. Current reporting of microglial activation in experimental studies of mTBI is non-standardized, which has limited our ability to identify concrete patterns of post-mTBI microglial activation over time. In this review, we examine preclinical studies of mTBI that report on microglial activation in white matter regions to summarize our current understanding of these patterns. Specifically, we summarize timecourses of post-mTBI microglial activation in white matter regions of the brain, identify factors that influence this activation, examine the temporal relationship between microglial activation and other post-mTBI assessments, and compare the relative sensitivities of various methods for detecting microglial activation. While the lack of replicated experimental conditions has limited the extent of conclusions that can confidently be drawn, we find that microglia are activated over a wide range of timecourses following mTBI and that microglial activation is a long-lasting outcome of mTBI that may resolve after most typical post-mTBI assessments, with the exception of those measuring oligodendrocyte lineage cell integrity. We identify several understudied parameters of post-mTBI microglial activation in white matter, such as the inclusion of female subjects. This review summarizes our current understanding of the progression of microglial activation in white matter structures following experimental mTBI and offers suggestions for important future research directions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01297-1. BioMed Central 2021-12-19 /pmc/articles/PMC8684664/ /pubmed/34924026 http://dx.doi.org/10.1186/s40478-021-01297-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Velayudhan, Prashanth S. Schwab, Nicole Hazrati, Lili-Naz Wheeler, Anne L. Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title | Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title_full | Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title_fullStr | Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title_full_unstemmed | Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title_short | Temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
title_sort | temporal patterns of microglial activation in white matter following experimental mild traumatic brain injury: a systematic literature review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684664/ https://www.ncbi.nlm.nih.gov/pubmed/34924026 http://dx.doi.org/10.1186/s40478-021-01297-1 |
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