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Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia

Reactive microgliosis is an important pathological component of neuroinflammation and has been implicated in a wide range of brain diseases including brain tumors, multiple sclerosis, Parkinson’s disease, Alzheimer’s disease, and schizophrenia. Mapping reactive microglia in-vivo is often performed w...

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Autores principales: Taquet, Maxime, Jankovski, Aleksandar, Rensonnet, Gaëtan, Jacobs, Damien, des Rieux, Anne, Macq, Benoît, Warfield, Simon K., Scherrer, Benoît
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761095/
https://www.ncbi.nlm.nih.gov/pubmed/31554896
http://dx.doi.org/10.1038/s41598-019-50432-5
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author Taquet, Maxime
Jankovski, Aleksandar
Rensonnet, Gaëtan
Jacobs, Damien
des Rieux, Anne
Macq, Benoît
Warfield, Simon K.
Scherrer, Benoît
author_facet Taquet, Maxime
Jankovski, Aleksandar
Rensonnet, Gaëtan
Jacobs, Damien
des Rieux, Anne
Macq, Benoît
Warfield, Simon K.
Scherrer, Benoît
author_sort Taquet, Maxime
collection PubMed
description Reactive microgliosis is an important pathological component of neuroinflammation and has been implicated in a wide range of brain diseases including brain tumors, multiple sclerosis, Parkinson’s disease, Alzheimer’s disease, and schizophrenia. Mapping reactive microglia in-vivo is often performed with PET scanning whose resolution, cost, and availability prevent its widespread use. The advent of diffusion compartment imaging (DCI) to probe tissue microstructure in vivo holds promise to map reactive microglia using MRI scanners. But this potential has never been demonstrated. In this paper, we performed longitudinal DCI in rats that underwent dorsal root axotomy triggering Wallerian degeneration of axons—a pathological process which reliably activates microglia. After the last DCI at 51 days, rats were sacrificed and histology with Iba-1 immunostaining for microglia was performed. The fraction of extra-axonal restricted diffusion from DCI was found to follow the expected temporal dynamics of reactive microgliosis. Furthermore, a strong and significant correlation between this parameter and histological measurement of microglial density was observed. These findings strongly suggest that extra-axonal restricted diffusion is an in-vivo marker of reactive microglia. They pave the way for MRI-based microglial mapping which may be important to characterize the pathogenesis of neurological and psychiatric diseases.
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spelling pubmed-67610952019-11-12 Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia Taquet, Maxime Jankovski, Aleksandar Rensonnet, Gaëtan Jacobs, Damien des Rieux, Anne Macq, Benoît Warfield, Simon K. Scherrer, Benoît Sci Rep Article Reactive microgliosis is an important pathological component of neuroinflammation and has been implicated in a wide range of brain diseases including brain tumors, multiple sclerosis, Parkinson’s disease, Alzheimer’s disease, and schizophrenia. Mapping reactive microglia in-vivo is often performed with PET scanning whose resolution, cost, and availability prevent its widespread use. The advent of diffusion compartment imaging (DCI) to probe tissue microstructure in vivo holds promise to map reactive microglia using MRI scanners. But this potential has never been demonstrated. In this paper, we performed longitudinal DCI in rats that underwent dorsal root axotomy triggering Wallerian degeneration of axons—a pathological process which reliably activates microglia. After the last DCI at 51 days, rats were sacrificed and histology with Iba-1 immunostaining for microglia was performed. The fraction of extra-axonal restricted diffusion from DCI was found to follow the expected temporal dynamics of reactive microgliosis. Furthermore, a strong and significant correlation between this parameter and histological measurement of microglial density was observed. These findings strongly suggest that extra-axonal restricted diffusion is an in-vivo marker of reactive microglia. They pave the way for MRI-based microglial mapping which may be important to characterize the pathogenesis of neurological and psychiatric diseases. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761095/ /pubmed/31554896 http://dx.doi.org/10.1038/s41598-019-50432-5 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Taquet, Maxime
Jankovski, Aleksandar
Rensonnet, Gaëtan
Jacobs, Damien
des Rieux, Anne
Macq, Benoît
Warfield, Simon K.
Scherrer, Benoît
Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title_full Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title_fullStr Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title_full_unstemmed Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title_short Extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
title_sort extra-axonal restricted diffusion as an in-vivo marker of reactive microglia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761095/
https://www.ncbi.nlm.nih.gov/pubmed/31554896
http://dx.doi.org/10.1038/s41598-019-50432-5
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