Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?

Spinal muscular atrophy (SMA) is a severe, inherited disease characterized by the progressive degeneration and death of motor neurons of the anterior horns of the spinal cord, which results in muscular atrophy and weakness of variable severity. Its early-onset form is invariably fatal in early child...

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Main Authors: Elena Abati, Gaia Citterio, Nereo Bresolin, Giacomo P. Comi, Stefania Corti
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:Neurobiology of Disease
Subjects:
SMA
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996120301455
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spelling doaj-03e1e58c91ec4b4ea2982632424356ea2021-03-22T08:41:52ZengElsevierNeurobiology of Disease1095-953X2020-07-01140104870Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?Elena Abati0Gaia Citterio1Nereo Bresolin2Giacomo P. Comi3Stefania Corti4Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, University of Milan, Milan, Italy.; Corresponding author.Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, University of Milan, Milan, Italy.Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, University of Milan, Milan, Italy.; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, University of Milan, Milan, Italy.; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, University of Milan, Milan, Italy.; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.; Correspondence to: S. Corti, Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section, Neurology Unit, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.Spinal muscular atrophy (SMA) is a severe, inherited disease characterized by the progressive degeneration and death of motor neurons of the anterior horns of the spinal cord, which results in muscular atrophy and weakness of variable severity. Its early-onset form is invariably fatal in early childhood, while milder forms lead to permanent disability, physical deformities and respiratory complications. Recently, two novel revolutionary therapies, antisense oligonucleotides and gene therapy, have been approved, and might prove successful in making long-term survival of these patients likely. In this perspective, a deep understanding of the pathogenic mechanisms and of their impact on the interactions between motor neurons and other cell types within the central nervous system (CNS) is crucial. Studies using SMA animal and cellular models have taught us that the survival and functionality of motor neurons is highly dependent on a whole range of other cell types, namely glial cells, which are responsible for a variety of different functions, such as neuronal trophic support, synaptic remodeling, and immune surveillance. Thus, it emerges that SMA is likely a non-cell autonomous, multifactorial disease in which the interaction of different cell types and disease mechanisms leads to motor neurons failure and loss. This review will introduce the different glial cell types in the CNS and provide an overview of the role of glial cells in motor neuron degeneration in SMA. Furthermore, we will discuss the relevance of these findings so far and the potential impact on the success of available therapies and on the development of novel ones.http://www.sciencedirect.com/science/article/pii/S0969996120301455Spinal muscular atrophySMAGliaNeuroinflammationAstrocytesMicroglia
collection DOAJ
language English
format Article
sources DOAJ
author Elena Abati
Gaia Citterio
Nereo Bresolin
Giacomo P. Comi
Stefania Corti
spellingShingle Elena Abati
Gaia Citterio
Nereo Bresolin
Giacomo P. Comi
Stefania Corti
Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
Neurobiology of Disease
Spinal muscular atrophy
SMA
Glia
Neuroinflammation
Astrocytes
Microglia
author_facet Elena Abati
Gaia Citterio
Nereo Bresolin
Giacomo P. Comi
Stefania Corti
author_sort Elena Abati
title Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
title_short Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
title_full Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
title_fullStr Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
title_full_unstemmed Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease?
title_sort glial cells involvement in spinal muscular atrophy: could sma be a neuroinflammatory disease?
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2020-07-01
description Spinal muscular atrophy (SMA) is a severe, inherited disease characterized by the progressive degeneration and death of motor neurons of the anterior horns of the spinal cord, which results in muscular atrophy and weakness of variable severity. Its early-onset form is invariably fatal in early childhood, while milder forms lead to permanent disability, physical deformities and respiratory complications. Recently, two novel revolutionary therapies, antisense oligonucleotides and gene therapy, have been approved, and might prove successful in making long-term survival of these patients likely. In this perspective, a deep understanding of the pathogenic mechanisms and of their impact on the interactions between motor neurons and other cell types within the central nervous system (CNS) is crucial. Studies using SMA animal and cellular models have taught us that the survival and functionality of motor neurons is highly dependent on a whole range of other cell types, namely glial cells, which are responsible for a variety of different functions, such as neuronal trophic support, synaptic remodeling, and immune surveillance. Thus, it emerges that SMA is likely a non-cell autonomous, multifactorial disease in which the interaction of different cell types and disease mechanisms leads to motor neurons failure and loss. This review will introduce the different glial cell types in the CNS and provide an overview of the role of glial cells in motor neuron degeneration in SMA. Furthermore, we will discuss the relevance of these findings so far and the potential impact on the success of available therapies and on the development of novel ones.
topic Spinal muscular atrophy
SMA
Glia
Neuroinflammation
Astrocytes
Microglia
url http://www.sciencedirect.com/science/article/pii/S0969996120301455
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