Glia Crosstalk in Neuroinflammatory Diseases

Neuroinflammation constitutes a fundamental cellular process to signal the loss of brain homeostasis. Glial cells play a central role in orchestrating these neuroinflammation processes in both deleterious and beneficial ways. These cellular responses depend on their intercellular interactions with n...

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Main Authors: Ada Bernaus, Sandra Blanco, Ana Sevilla
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-07-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fncel.2020.00209/full
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author Ada Bernaus
Sandra Blanco
Sandra Blanco
Ana Sevilla
author_facet Ada Bernaus
Sandra Blanco
Sandra Blanco
Ana Sevilla
author_sort Ada Bernaus
collection DOAJ
description Neuroinflammation constitutes a fundamental cellular process to signal the loss of brain homeostasis. Glial cells play a central role in orchestrating these neuroinflammation processes in both deleterious and beneficial ways. These cellular responses depend on their intercellular interactions with neurons, astrocytes, the blood–brain barrier (BBB), and infiltrated T cells in the central nervous system (CNS). However, this intercellular crosstalk seems to be activated by specific stimuli for each different neurological scenario. This review summarizes key studies linking neuroinflammation with certain neurodegenerative diseases such as Alzheimer disease (AD), Parkinson disease (PD), and amyotrophic lateral sclerosis (ALS) and for the development of better therapeutic strategies based on immunomodulation.
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spelling doaj.art-67dc094529db4c5bb4e08d72fc6fbb992022-12-21T18:25:01ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022020-07-011410.3389/fncel.2020.00209539179Glia Crosstalk in Neuroinflammatory DiseasesAda Bernaus0Sandra Blanco1Sandra Blanco2Ana Sevilla3Departament de Biologia Cellular, Fisiologia i Immunologia, Facultat de Biologia, Universitat de Barcelona, Barcelona, SpainMolecular Mechanisms Program, Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas (CSIC), University of Salamanca, Salamanca, SpainInstituto de Investigación Biomédica de Salamanca (IBSAL), Hospital Universitario de Salamanca, Salamanca, SpainDepartament de Biologia Cellular, Fisiologia i Immunologia, Facultat de Biologia, Universitat de Barcelona, Barcelona, SpainNeuroinflammation constitutes a fundamental cellular process to signal the loss of brain homeostasis. Glial cells play a central role in orchestrating these neuroinflammation processes in both deleterious and beneficial ways. These cellular responses depend on their intercellular interactions with neurons, astrocytes, the blood–brain barrier (BBB), and infiltrated T cells in the central nervous system (CNS). However, this intercellular crosstalk seems to be activated by specific stimuli for each different neurological scenario. This review summarizes key studies linking neuroinflammation with certain neurodegenerative diseases such as Alzheimer disease (AD), Parkinson disease (PD), and amyotrophic lateral sclerosis (ALS) and for the development of better therapeutic strategies based on immunomodulation.https://www.frontiersin.org/article/10.3389/fncel.2020.00209/fullneurodegenerationastrogliosismicrogliaproteinopathiesAlzheimer diseaseParkinson disease
spellingShingle Ada Bernaus
Sandra Blanco
Sandra Blanco
Ana Sevilla
Glia Crosstalk in Neuroinflammatory Diseases
Frontiers in Cellular Neuroscience
neurodegeneration
astrogliosis
microglia
proteinopathies
Alzheimer disease
Parkinson disease
title Glia Crosstalk in Neuroinflammatory Diseases
title_full Glia Crosstalk in Neuroinflammatory Diseases
title_fullStr Glia Crosstalk in Neuroinflammatory Diseases
title_full_unstemmed Glia Crosstalk in Neuroinflammatory Diseases
title_short Glia Crosstalk in Neuroinflammatory Diseases
title_sort glia crosstalk in neuroinflammatory diseases
topic neurodegeneration
astrogliosis
microglia
proteinopathies
Alzheimer disease
Parkinson disease
url https://www.frontiersin.org/article/10.3389/fncel.2020.00209/full
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AT sandrablanco gliacrosstalkinneuroinflammatorydiseases
AT sandrablanco gliacrosstalkinneuroinflammatorydiseases
AT anasevilla gliacrosstalkinneuroinflammatorydiseases