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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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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