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TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration

At the neuromuscular junction (NMJ), motor neurons and myocytes maintain a bidirectional communication that guarantees adequate functionality. Thus, motor neurons’ firing pattern, which is influenced by retrograde muscle-derived neurotrophic factors, modulates myocyte contractibility. Myocytes can b...

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Autores principales: Just-Borràs, Laia, Cilleros-Mañé, Víctor, Polishchuk, Aleksandra, Balanyà-Segura, Marta, Tomàs, Marta, Garcia, Neus, Tomàs, Josep, Lanuza, Maria A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813967/
https://www.ncbi.nlm.nih.gov/pubmed/36618825
http://dx.doi.org/10.3389/fnmol.2022.1069940
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author Just-Borràs, Laia
Cilleros-Mañé, Víctor
Polishchuk, Aleksandra
Balanyà-Segura, Marta
Tomàs, Marta
Garcia, Neus
Tomàs, Josep
Lanuza, Maria A.
author_facet Just-Borràs, Laia
Cilleros-Mañé, Víctor
Polishchuk, Aleksandra
Balanyà-Segura, Marta
Tomàs, Marta
Garcia, Neus
Tomàs, Josep
Lanuza, Maria A.
author_sort Just-Borràs, Laia
collection PubMed
description At the neuromuscular junction (NMJ), motor neurons and myocytes maintain a bidirectional communication that guarantees adequate functionality. Thus, motor neurons’ firing pattern, which is influenced by retrograde muscle-derived neurotrophic factors, modulates myocyte contractibility. Myocytes can be fast-twitch fibers and become easily fatigued or slow-twitch fibers and resistant to fatigue. Extraocular muscles (EOM) show mixed properties that guarantee fast contraction speed and resistance to fatigue and the degeneration caused by Amyotrophic lateral sclerosis (ALS) disease. The TrkB signaling is an activity-dependent pathway implicated in the NMJ well-functioning. Therefore, it could mediate the differences between fast and slow myocytes’ resistance to fatigue. The present study elucidates a specific protein expression profile concerning the TrkB signaling that correlates with higher resistance to fatigue and better neuroprotective capacity through time. The results unveil that Extra-ocular muscles (EOM) express lower levels of NT-4 that extend TrkB signaling, differential PKC expression, and a higher abundance of phosphorylated synaptic proteins that correlate with continuous neurotransmission requirements. Furthermore, common molecular features between EOM and slow soleus muscles including higher neurotrophic consumption and classic and novel PKC isoforms balance correlate with better preservation of these two muscles in ALS. Altogether, higher resistance of Soleus and EOM to fatigue and ALS seems to be associated with specific protein levels concerning the TrkB neurotrophic signaling.
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spelling pubmed-98139672023-01-06 TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration Just-Borràs, Laia Cilleros-Mañé, Víctor Polishchuk, Aleksandra Balanyà-Segura, Marta Tomàs, Marta Garcia, Neus Tomàs, Josep Lanuza, Maria A. Front Mol Neurosci Neuroscience At the neuromuscular junction (NMJ), motor neurons and myocytes maintain a bidirectional communication that guarantees adequate functionality. Thus, motor neurons’ firing pattern, which is influenced by retrograde muscle-derived neurotrophic factors, modulates myocyte contractibility. Myocytes can be fast-twitch fibers and become easily fatigued or slow-twitch fibers and resistant to fatigue. Extraocular muscles (EOM) show mixed properties that guarantee fast contraction speed and resistance to fatigue and the degeneration caused by Amyotrophic lateral sclerosis (ALS) disease. The TrkB signaling is an activity-dependent pathway implicated in the NMJ well-functioning. Therefore, it could mediate the differences between fast and slow myocytes’ resistance to fatigue. The present study elucidates a specific protein expression profile concerning the TrkB signaling that correlates with higher resistance to fatigue and better neuroprotective capacity through time. The results unveil that Extra-ocular muscles (EOM) express lower levels of NT-4 that extend TrkB signaling, differential PKC expression, and a higher abundance of phosphorylated synaptic proteins that correlate with continuous neurotransmission requirements. Furthermore, common molecular features between EOM and slow soleus muscles including higher neurotrophic consumption and classic and novel PKC isoforms balance correlate with better preservation of these two muscles in ALS. Altogether, higher resistance of Soleus and EOM to fatigue and ALS seems to be associated with specific protein levels concerning the TrkB neurotrophic signaling. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9813967/ /pubmed/36618825 http://dx.doi.org/10.3389/fnmol.2022.1069940 Text en Copyright © 2022 Just-Borràs, Cilleros-Mañé, Polishchuk, Balanyà-Segura, Tomàs, Garcia, Tomàs and Lanuza. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Just-Borràs, Laia
Cilleros-Mañé, Víctor
Polishchuk, Aleksandra
Balanyà-Segura, Marta
Tomàs, Marta
Garcia, Neus
Tomàs, Josep
Lanuza, Maria A.
TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title_full TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title_fullStr TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title_full_unstemmed TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title_short TrkB signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
title_sort trkb signaling is correlated with muscular fatigue resistance and less vulnerability to neurodegeneration
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813967/
https://www.ncbi.nlm.nih.gov/pubmed/36618825
http://dx.doi.org/10.3389/fnmol.2022.1069940
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