Cargando…

Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression

Laminin-α4 is involved in the alignment of active zones to postjunctional folds at the neuromuscular junction (NMJ). Prior study has implicated laminin-α4 in NMJ maintenance, with altered NMJ morphology observed in adult laminin-α4 deficient mice (lama4(−/−)). The present study further investigated...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Kah Meng, Chand, Kirat K., Hammond, Luke A., Lavidis, Nickolas A., Noakes, Peter G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391237/
https://www.ncbi.nlm.nih.gov/pubmed/28301326
http://dx.doi.org/10.18632/aging.101198
_version_ 1783229246035984384
author Lee, Kah Meng
Chand, Kirat K.
Hammond, Luke A.
Lavidis, Nickolas A.
Noakes, Peter G.
author_facet Lee, Kah Meng
Chand, Kirat K.
Hammond, Luke A.
Lavidis, Nickolas A.
Noakes, Peter G.
author_sort Lee, Kah Meng
collection PubMed
description Laminin-α4 is involved in the alignment of active zones to postjunctional folds at the neuromuscular junction (NMJ). Prior study has implicated laminin-α4 in NMJ maintenance, with altered NMJ morphology observed in adult laminin-α4 deficient mice (lama4(−/−)). The present study further investigated the role of laminin-α4 in NMJ maintenance by functional characterization of transmission properties, morphological investigation of synaptic proteins including synaptic laminin-α4, and neuromotor behavioral testing. Results showed maintained perturbed transmission properties at lama4(−/−) NMJs from adult (3 months) through to aged (18-22 months). Hind-limb grip force demonstrated similar trends as transmission properties, with maintained weaker grip force across age groups in lama4(−/−). Interestingly, both transmission properties and hind-limb grip force in aged wild-types resembled those observed in adult lama4(−/−). Most significantly, altered expression of laminin-α4 was noted at the wild-type NMJs prior to the observed decline in transmission properties, suggesting that altered laminin-α4 expression precedes the decline of neurotransmission in aging wild-types. These findings significantly support the role of laminin-α4 in maintenance of the NMJ during aging.
format Online
Article
Text
id pubmed-5391237
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-53912372017-04-20 Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression Lee, Kah Meng Chand, Kirat K. Hammond, Luke A. Lavidis, Nickolas A. Noakes, Peter G. Aging (Albany NY) Research Paper Laminin-α4 is involved in the alignment of active zones to postjunctional folds at the neuromuscular junction (NMJ). Prior study has implicated laminin-α4 in NMJ maintenance, with altered NMJ morphology observed in adult laminin-α4 deficient mice (lama4(−/−)). The present study further investigated the role of laminin-α4 in NMJ maintenance by functional characterization of transmission properties, morphological investigation of synaptic proteins including synaptic laminin-α4, and neuromotor behavioral testing. Results showed maintained perturbed transmission properties at lama4(−/−) NMJs from adult (3 months) through to aged (18-22 months). Hind-limb grip force demonstrated similar trends as transmission properties, with maintained weaker grip force across age groups in lama4(−/−). Interestingly, both transmission properties and hind-limb grip force in aged wild-types resembled those observed in adult lama4(−/−). Most significantly, altered expression of laminin-α4 was noted at the wild-type NMJs prior to the observed decline in transmission properties, suggesting that altered laminin-α4 expression precedes the decline of neurotransmission in aging wild-types. These findings significantly support the role of laminin-α4 in maintenance of the NMJ during aging. Impact Journals LLC 2017-03-14 /pmc/articles/PMC5391237/ /pubmed/28301326 http://dx.doi.org/10.18632/aging.101198 Text en Copyright: © 2017 Lee et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Lee, Kah Meng
Chand, Kirat K.
Hammond, Luke A.
Lavidis, Nickolas A.
Noakes, Peter G.
Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title_full Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title_fullStr Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title_full_unstemmed Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title_short Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
title_sort functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391237/
https://www.ncbi.nlm.nih.gov/pubmed/28301326
http://dx.doi.org/10.18632/aging.101198
work_keys_str_mv AT leekahmeng functionaldeclineattheagingneuromuscularjunctionisassociatedwithalteredlaminina4expression
AT chandkiratk functionaldeclineattheagingneuromuscularjunctionisassociatedwithalteredlaminina4expression
AT hammondlukea functionaldeclineattheagingneuromuscularjunctionisassociatedwithalteredlaminina4expression
AT lavidisnickolasa functionaldeclineattheagingneuromuscularjunctionisassociatedwithalteredlaminina4expression
AT noakespeterg functionaldeclineattheagingneuromuscularjunctionisassociatedwithalteredlaminina4expression