Cargando…

Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice

Spinal muscular atrophy results from diminished levels of survival motor neuron (SMN) protein in spinal motor neurons. Low levels of SMN also occur in models of amyotrophic lateral sclerosis (ALS) caused by mutant superoxide dismutase 1 (SOD1) and genetic reduction of SMN levels exacerbates the phen...

Descripción completa

Detalles Bibliográficos
Autores principales: Turner, Bradley J., Alfazema, Neza, Sheean, Rebecca K., Sleigh, James N., Davies, Kay E., Horne, Malcolm K., Talbot, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919158/
https://www.ncbi.nlm.nih.gov/pubmed/24210254
http://dx.doi.org/10.1016/j.neurobiolaging.2013.09.030
_version_ 1782303028214235136
author Turner, Bradley J.
Alfazema, Neza
Sheean, Rebecca K.
Sleigh, James N.
Davies, Kay E.
Horne, Malcolm K.
Talbot, Kevin
author_facet Turner, Bradley J.
Alfazema, Neza
Sheean, Rebecca K.
Sleigh, James N.
Davies, Kay E.
Horne, Malcolm K.
Talbot, Kevin
author_sort Turner, Bradley J.
collection PubMed
description Spinal muscular atrophy results from diminished levels of survival motor neuron (SMN) protein in spinal motor neurons. Low levels of SMN also occur in models of amyotrophic lateral sclerosis (ALS) caused by mutant superoxide dismutase 1 (SOD1) and genetic reduction of SMN levels exacerbates the phenotype of transgenic SOD1(G93A) mice. Here, we demonstrate that SMN protein is significantly reduced in the spinal cords of patients with sporadic ALS. To test the potential of SMN as a modifier of ALS, we overexpressed SMN in 2 different strains of SOD1(G93A) mice. Neuronal overexpression of SMN significantly preserved locomotor function, rescued motor neurons, and attenuated astrogliosis in spinal cords of SOD1(G93A) mice. Despite this, survival was not prolonged, most likely resulting from SMN mislocalization and depletion of gems in motor neurons of symptomatic mice. Our results reveal that SMN upregulation slows locomotor deficit onset and motor neuron loss in this mouse model of ALS. However, disruption of SMN nuclear complexes by high levels of mutant SOD1, even in the presence of SMN overexpression, might limit its survival promoting effects in this specific mouse model. Studies in emerging mouse models of ALS are therefore warranted to further explore the potential of SMN as a modifier of ALS.
format Online
Article
Text
id pubmed-3919158
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-39191582014-04-01 Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice Turner, Bradley J. Alfazema, Neza Sheean, Rebecca K. Sleigh, James N. Davies, Kay E. Horne, Malcolm K. Talbot, Kevin Neurobiol Aging Regular Article Spinal muscular atrophy results from diminished levels of survival motor neuron (SMN) protein in spinal motor neurons. Low levels of SMN also occur in models of amyotrophic lateral sclerosis (ALS) caused by mutant superoxide dismutase 1 (SOD1) and genetic reduction of SMN levels exacerbates the phenotype of transgenic SOD1(G93A) mice. Here, we demonstrate that SMN protein is significantly reduced in the spinal cords of patients with sporadic ALS. To test the potential of SMN as a modifier of ALS, we overexpressed SMN in 2 different strains of SOD1(G93A) mice. Neuronal overexpression of SMN significantly preserved locomotor function, rescued motor neurons, and attenuated astrogliosis in spinal cords of SOD1(G93A) mice. Despite this, survival was not prolonged, most likely resulting from SMN mislocalization and depletion of gems in motor neurons of symptomatic mice. Our results reveal that SMN upregulation slows locomotor deficit onset and motor neuron loss in this mouse model of ALS. However, disruption of SMN nuclear complexes by high levels of mutant SOD1, even in the presence of SMN overexpression, might limit its survival promoting effects in this specific mouse model. Studies in emerging mouse models of ALS are therefore warranted to further explore the potential of SMN as a modifier of ALS. Elsevier 2014-04 /pmc/articles/PMC3919158/ /pubmed/24210254 http://dx.doi.org/10.1016/j.neurobiolaging.2013.09.030 Text en © 2014 Elsevier Inc. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Regular Article
Turner, Bradley J.
Alfazema, Neza
Sheean, Rebecca K.
Sleigh, James N.
Davies, Kay E.
Horne, Malcolm K.
Talbot, Kevin
Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title_full Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title_fullStr Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title_full_unstemmed Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title_short Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
title_sort overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant sod1 mice
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919158/
https://www.ncbi.nlm.nih.gov/pubmed/24210254
http://dx.doi.org/10.1016/j.neurobiolaging.2013.09.030
work_keys_str_mv AT turnerbradleyj overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT alfazemaneza overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT sheeanrebeccak overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT sleighjamesn overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT davieskaye overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT hornemalcolmk overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice
AT talbotkevin overexpressionofsurvivalmotorneuronimprovesneuromuscularfunctionandmotorneuronsurvivalinmutantsod1mice