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In Vivo Imaging of Microglia With Multiphoton Microscopy

Neuroimaging has become an unparalleled tool to understand the central nervous system (CNS) anatomy, physiology and neurological diseases. While an altered immune function and microglia hyperactivation are common neuropathological features for many CNS disorders and neurodegenerative diseases, direc...

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Autores principales: Hierro-Bujalance, Carmen, Bacskai, Brian J., Garcia-Alloza, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060250/
https://www.ncbi.nlm.nih.gov/pubmed/30072888
http://dx.doi.org/10.3389/fnagi.2018.00218
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author Hierro-Bujalance, Carmen
Bacskai, Brian J.
Garcia-Alloza, Monica
author_facet Hierro-Bujalance, Carmen
Bacskai, Brian J.
Garcia-Alloza, Monica
author_sort Hierro-Bujalance, Carmen
collection PubMed
description Neuroimaging has become an unparalleled tool to understand the central nervous system (CNS) anatomy, physiology and neurological diseases. While an altered immune function and microglia hyperactivation are common neuropathological features for many CNS disorders and neurodegenerative diseases, direct assessment of the role of microglial cells remains a challenging task. Non-invasive neuroimaging techniques, including magnetic resonance imaging (MRI), positron emission tomography (PET) and single positron emission computed tomography (SPECT) are widely used for human clinical applications, and a variety of ligands are available to detect neuroinflammation. In animal models, intravital imaging has been largely used, and minimally invasive multiphoton microcopy (MPM) provides high resolution detection of single microglia cells, longitudinally, in living brain. In this study, we review in vivo real-time MPM approaches to assess microglia in preclinical studies, including individual cell responses in surveillance, support, protection and restoration of brain tissue integrity, synapse formation, homeostasis, as well as in different pathological situations. We focus on in vivo studies that assess the role of microglia in mouse models of Alzheimer’s disease (AD), analyzing microglial motility and recruitment, as well as the role of microglia in anti-amyloid-β treatment, as a key therapeutic approach to treat AD. Altogether, MPM provides a high contrast and high spatial resolution approach to follow microglia chronically in vivo in complex models, supporting MPM as a powerful tool for deep intravital tissue imaging.
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spelling pubmed-60602502018-08-02 In Vivo Imaging of Microglia With Multiphoton Microscopy Hierro-Bujalance, Carmen Bacskai, Brian J. Garcia-Alloza, Monica Front Aging Neurosci Neuroscience Neuroimaging has become an unparalleled tool to understand the central nervous system (CNS) anatomy, physiology and neurological diseases. While an altered immune function and microglia hyperactivation are common neuropathological features for many CNS disorders and neurodegenerative diseases, direct assessment of the role of microglial cells remains a challenging task. Non-invasive neuroimaging techniques, including magnetic resonance imaging (MRI), positron emission tomography (PET) and single positron emission computed tomography (SPECT) are widely used for human clinical applications, and a variety of ligands are available to detect neuroinflammation. In animal models, intravital imaging has been largely used, and minimally invasive multiphoton microcopy (MPM) provides high resolution detection of single microglia cells, longitudinally, in living brain. In this study, we review in vivo real-time MPM approaches to assess microglia in preclinical studies, including individual cell responses in surveillance, support, protection and restoration of brain tissue integrity, synapse formation, homeostasis, as well as in different pathological situations. We focus on in vivo studies that assess the role of microglia in mouse models of Alzheimer’s disease (AD), analyzing microglial motility and recruitment, as well as the role of microglia in anti-amyloid-β treatment, as a key therapeutic approach to treat AD. Altogether, MPM provides a high contrast and high spatial resolution approach to follow microglia chronically in vivo in complex models, supporting MPM as a powerful tool for deep intravital tissue imaging. Frontiers Media S.A. 2018-07-19 /pmc/articles/PMC6060250/ /pubmed/30072888 http://dx.doi.org/10.3389/fnagi.2018.00218 Text en Copyright © 2018 Hierro-Bujalance, Bacskai and Garcia-Alloza. http://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 Neuroscience
Hierro-Bujalance, Carmen
Bacskai, Brian J.
Garcia-Alloza, Monica
In Vivo Imaging of Microglia With Multiphoton Microscopy
title In Vivo Imaging of Microglia With Multiphoton Microscopy
title_full In Vivo Imaging of Microglia With Multiphoton Microscopy
title_fullStr In Vivo Imaging of Microglia With Multiphoton Microscopy
title_full_unstemmed In Vivo Imaging of Microglia With Multiphoton Microscopy
title_short In Vivo Imaging of Microglia With Multiphoton Microscopy
title_sort in vivo imaging of microglia with multiphoton microscopy
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060250/
https://www.ncbi.nlm.nih.gov/pubmed/30072888
http://dx.doi.org/10.3389/fnagi.2018.00218
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