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In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury

Microglia, the innate immune sentinels of the central nervous system, are the most dynamic cells in the brain parenchyma. They are the first responders to insult and mediate neuroinflammation. Following cellular damage, microglia extend their processes towards the lesion, modify their morphology, re...

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Detalles Bibliográficos
Autores principales: Tvrdik, Petr, Kalani, M. Yashar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713335/
https://www.ncbi.nlm.nih.gov/pubmed/29117112
http://dx.doi.org/10.3390/ijms18112366
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author Tvrdik, Petr
Kalani, M. Yashar S.
author_facet Tvrdik, Petr
Kalani, M. Yashar S.
author_sort Tvrdik, Petr
collection PubMed
description Microglia, the innate immune sentinels of the central nervous system, are the most dynamic cells in the brain parenchyma. They are the first responders to insult and mediate neuroinflammation. Following cellular damage, microglia extend their processes towards the lesion, modify their morphology, release cytokines and other mediators, and eventually migrate towards the damaged area and remove cellular debris by phagocytosis. Intracellular Ca(2+) signaling plays important roles in many of these functions. However, Ca(2+) in microglia has not been systematically studied in vivo. Here we review recent findings using genetically encoded Ca(2+) indicators and two-photon imaging, which have enabled new insights into Ca(2+) dynamics and signaling pathways in large populations of microglia in vivo. These new approaches will help to evaluate pre-clinical interventions and immunomodulation for pathological brain conditions such as stroke and neurodegenerative diseases.
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spelling pubmed-57133352017-12-07 In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury Tvrdik, Petr Kalani, M. Yashar S. Int J Mol Sci Review Microglia, the innate immune sentinels of the central nervous system, are the most dynamic cells in the brain parenchyma. They are the first responders to insult and mediate neuroinflammation. Following cellular damage, microglia extend their processes towards the lesion, modify their morphology, release cytokines and other mediators, and eventually migrate towards the damaged area and remove cellular debris by phagocytosis. Intracellular Ca(2+) signaling plays important roles in many of these functions. However, Ca(2+) in microglia has not been systematically studied in vivo. Here we review recent findings using genetically encoded Ca(2+) indicators and two-photon imaging, which have enabled new insights into Ca(2+) dynamics and signaling pathways in large populations of microglia in vivo. These new approaches will help to evaluate pre-clinical interventions and immunomodulation for pathological brain conditions such as stroke and neurodegenerative diseases. MDPI 2017-11-08 /pmc/articles/PMC5713335/ /pubmed/29117112 http://dx.doi.org/10.3390/ijms18112366 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tvrdik, Petr
Kalani, M. Yashar S.
In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title_full In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title_fullStr In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title_full_unstemmed In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title_short In Vivo Imaging of Microglial Calcium Signaling in Brain Inflammation and Injury
title_sort in vivo imaging of microglial calcium signaling in brain inflammation and injury
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713335/
https://www.ncbi.nlm.nih.gov/pubmed/29117112
http://dx.doi.org/10.3390/ijms18112366
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