Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis

The biology of brain microvascular pericytes is an active area of research and discovery, as their interaction with the endothelium is critical for multiple aspects of cerebrovascular function. There is growing evidence that pericyte loss or dysfunction is involved in the pathogenesis of Alzheimer’s...

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Main Authors: Andrée-Anne Berthiaume, David A. Hartmann, Mark W. Majesky, Narayan R. Bhat, Andy Y. Shih
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-07-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnagi.2018.00210/full
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author Andrée-Anne Berthiaume
David A. Hartmann
Mark W. Majesky
Mark W. Majesky
Narayan R. Bhat
Andy Y. Shih
Andy Y. Shih
Andy Y. Shih
author_facet Andrée-Anne Berthiaume
David A. Hartmann
Mark W. Majesky
Mark W. Majesky
Narayan R. Bhat
Andy Y. Shih
Andy Y. Shih
Andy Y. Shih
author_sort Andrée-Anne Berthiaume
collection DOAJ
description The biology of brain microvascular pericytes is an active area of research and discovery, as their interaction with the endothelium is critical for multiple aspects of cerebrovascular function. There is growing evidence that pericyte loss or dysfunction is involved in the pathogenesis of Alzheimer’s disease, vascular dementia, ischemic stroke and brain injury. However, strategies to mitigate or compensate for this loss remain limited. In this review, we highlight a novel finding that pericytes in the adult brain are structurally dynamic in vivo, and actively compensate for loss of endothelial coverage by extending their far-reaching processes to maintain contact with regions of exposed endothelium. Structural remodeling of pericytes may present an opportunity to foster pericyte-endothelial communication in the adult brain and should be explored as a potential means to counteract pericyte loss in dementia and cerebrovascular disease. We discuss the pathophysiological consequences of pericyte loss on capillary function, and the biochemical pathways that may control pericyte remodeling. We also offer guidance for observing pericytes in vivo, such that pericyte structural remodeling can be more broadly studied in mouse models of cerebrovascular disease.
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spelling doaj.art-b171019522f946e0ab68ba37cb0cede32022-12-22T02:11:12ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652018-07-011010.3389/fnagi.2018.00210386442Pericyte Structural Remodeling in Cerebrovascular Health and HomeostasisAndrée-Anne Berthiaume0David A. Hartmann1Mark W. Majesky2Mark W. Majesky3Narayan R. Bhat4Andy Y. Shih5Andy Y. Shih6Andy Y. Shih7Department of Neuroscience, Medical University of South Carolina, Charleston, SC, United StatesDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC, United StatesCenter for Developmental Biology and Regenerative Medicine, Seattle Children’s Research Institute, Seattle, WA, United StatesDepartments of Pediatrics and Pathology, University of Washington, Seattle, WA, United StatesDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC, United StatesDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC, United StatesCenter for Developmental Biology and Regenerative Medicine, Seattle Children’s Research Institute, Seattle, WA, United StatesCenter for Biomedical Imaging, Medical University of South Carolina, Charleston, SC, United StatesThe biology of brain microvascular pericytes is an active area of research and discovery, as their interaction with the endothelium is critical for multiple aspects of cerebrovascular function. There is growing evidence that pericyte loss or dysfunction is involved in the pathogenesis of Alzheimer’s disease, vascular dementia, ischemic stroke and brain injury. However, strategies to mitigate or compensate for this loss remain limited. In this review, we highlight a novel finding that pericytes in the adult brain are structurally dynamic in vivo, and actively compensate for loss of endothelial coverage by extending their far-reaching processes to maintain contact with regions of exposed endothelium. Structural remodeling of pericytes may present an opportunity to foster pericyte-endothelial communication in the adult brain and should be explored as a potential means to counteract pericyte loss in dementia and cerebrovascular disease. We discuss the pathophysiological consequences of pericyte loss on capillary function, and the biochemical pathways that may control pericyte remodeling. We also offer guidance for observing pericytes in vivo, such that pericyte structural remodeling can be more broadly studied in mouse models of cerebrovascular disease.https://www.frontiersin.org/article/10.3389/fnagi.2018.00210/fullpericytetwo-photon imagingcapillary blood flowblood-brain barrierAlzheimer’s diseasemural cell
spellingShingle Andrée-Anne Berthiaume
David A. Hartmann
Mark W. Majesky
Mark W. Majesky
Narayan R. Bhat
Andy Y. Shih
Andy Y. Shih
Andy Y. Shih
Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
Frontiers in Aging Neuroscience
pericyte
two-photon imaging
capillary blood flow
blood-brain barrier
Alzheimer’s disease
mural cell
title Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
title_full Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
title_fullStr Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
title_full_unstemmed Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
title_short Pericyte Structural Remodeling in Cerebrovascular Health and Homeostasis
title_sort pericyte structural remodeling in cerebrovascular health and homeostasis
topic pericyte
two-photon imaging
capillary blood flow
blood-brain barrier
Alzheimer’s disease
mural cell
url https://www.frontiersin.org/article/10.3389/fnagi.2018.00210/full
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