Articles producció científicaCiències Mèdiques Bàsiques

Running and swimming prevent the deregulation of the BDNF/TrkB neurotrophic signalling at the neuromuscular junction in mice with amyotrophic lateral sclerosis

  • Dades identificatives

    Identificador:  imarina:5927143
    Autors:  Just-Borras, Laia; Hurtado, Erica; Cilleros-Mane, Victor; Biondi, Olivier; Charbonnier, Frederic; Tomas, Marta; Garcia, Neus; Tomas, Josep; Lanuza, Maria A
    Resum:
    Nerve-induced muscle contraction regulates the BDNF/TrkB neurotrophic signalling to retrogradely modulate neurotransmission and protect the neuromuscular junctions and motoneurons. In muscles with amyotrophic lateral sclerosis, this pathway is strongly misbalanced and neuromuscular junctions are destabilized, which may directly cause the motoneuron degeneration and muscular atrophy observed in this disease. Here, we sought to demonstrate (1) that physical exercise, whose recommendation has been controversial in amyotrophic lateral sclerosis, would be a good option for its therapy, because it normalizes and improves the altered neurotrophin pathway and (2) a plausible molecular mechanism underlying its positive effect. SOD1-G93A mice were trained following either running or swimming-based protocols since the beginning of the symptomatic phase (day 70 of age) until day 115. Next, the full BDNF pathway, including receptors, downstream kinases and proteins related with neurotransmission, was characterized and motoneuron survival was analysed. The results establish that amyotrophic lateral sclerosis-induced damaging molecular changes in the BDNF/TrkB pathway are reduced, prevented or even overcompensated by precisely defined exercise protocols that modulate TrkB isoforms and neurotransmission regulatory proteins and reduce motoneuron death. Altogether, the maintenance of the BDNF/TrkB signalling and the downstream pathway, particularly after the swimming protocol, adds new molecular evidence of the benefits of physical exercise to reduce the impact of amyotrophic lateral sclerosis. These results are encouraging since they reveal an improvement even starting the therapy after the onset of the disease.
  • Altres:

    Autor segons l'article: Just-Borras, Laia; Hurtado, Erica; Cilleros-Mane, Victor; Biondi, Olivier; Charbonnier, Frederic; Tomas, Marta; Garcia, Neus; Tomas, Josep; Lanuza, Maria A
    Departament: Ciències Mèdiques Bàsiques
    e-ISSN: 3027-3040
    Autor/s de la URV: Cilleros Mañé, Víctor / Garcia Sancho, Maria de les Neus / Hurtado Caballero, Erica / Just Borràs, Laia / Lanuza Escolano, María Angel / Tomás Ferré, José Maria / Tomas Marginet, Marta / Tomàs Porres, Josep
    Paraules clau: Trkb receptors; Transgenic mouse model; Swimming; Superoxide dismutase-1; Sod1 protein, mouse; Sod1; Snare proteins; Skeletal-muscle; Skeletal muscle; Signal transduction; Selective vulnerability; Protein-tyrosine kinases; Protein kinase c-alpha; Protein isoforms; Polymorphism, single nucleotide; Physical-activity; Physical conditioning, animal; Ntrk2 protein, mouse; Nmj; Neurotransmission; Neuromuscular junction; Muscle, skeletal; Motor-neurons; Motor neurons; Motoneuron survival; Motoneuron loss; Mice, transgenic; Mice; Membrane glycoproteins; Male; Female; Exercise; Disease models, animal; Brain-derived neurotrophic factor; Bdnf; Animals; Amyotrophic lateral sclerosis; Als; nmj; neurotransmission; motoneuron loss; exercise; als
    Resum: Nerve-induced muscle contraction regulates the BDNF/TrkB neurotrophic signalling to retrogradely modulate neurotransmission and protect the neuromuscular junctions and motoneurons. In muscles with amyotrophic lateral sclerosis, this pathway is strongly misbalanced and neuromuscular junctions are destabilized, which may directly cause the motoneuron degeneration and muscular atrophy observed in this disease. Here, we sought to demonstrate (1) that physical exercise, whose recommendation has been controversial in amyotrophic lateral sclerosis, would be a good option for its therapy, because it normalizes and improves the altered neurotrophin pathway and (2) a plausible molecular mechanism underlying its positive effect. SOD1-G93A mice were trained following either running or swimming-based protocols since the beginning of the symptomatic phase (day 70 of age) until day 115. Next, the full BDNF pathway, including receptors, downstream kinases and proteins related with neurotransmission, was characterized and motoneuron survival was analysed. The results establish that amyotrophic lateral sclerosis-induced damaging molecular changes in the BDNF/TrkB pathway are reduced, prevented or even overcompensated by precisely defined exercise protocols that modulate TrkB isoforms and neurotransmission regulatory proteins and reduce motoneuron death. Altogether, the maintenance of the BDNF/TrkB signalling and the downstream pathway, particularly after the swimming protocol, adds new molecular evidence of the benefits of physical exercise to reduce the impact of amyotrophic lateral sclerosis. These results are encouraging since they reveal an improvement even starting the therapy after the onset of the disease.
    Grup de recerca: Unitat d'Histologia i Neurobiologia
    Àrees temàtiques: Pharmacology; Molecular medicine; Molecular biology; Medicina ii; Medicina i; General medicine; Farmacia; Ensino; Educação física; Ciências biológicas iii; Ciências biológicas ii; Ciências biológicas i; Cellular and molecular neuroscience; Cell biology; Biotecnología; Biology; Biochemistry & molecular biology; Astronomia / física
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: laia.just@urv.cat; marta.tomas@urv.cat; erica.hurtado@urv.cat; josep.tomaspo@estudiants.urv.cat; victor.cilleros@alumni.urv.cat; josepmaria.tomas@urv.cat; laia.just@urv.cat; mariaangel.lanuza@urv.cat
    ISSN: 1420682X
    Data d'alta del registre: 2025-01-08
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://pmc.ncbi.nlm.nih.gov/articles/PMC11104938/pdf/18_2019_Article_3337.pdf
    Referència a l'article segons font original: Cellular And Molecular Life Sciences. 77 (15): 3027-3040
    Referència de l'ítem segons les normes APA: Just-Borras, Laia; Hurtado, Erica; Cilleros-Mane, Victor; Biondi, Olivier; Charbonnier, Frederic; Tomas, Marta; Garcia, Neus; Tomas, Josep; Lanuza, Ma (2020). Running and swimming prevent the deregulation of the BDNF/TrkB neurotrophic signalling at the neuromuscular junction in mice with amyotrophic lateral sclerosis. Cellular And Molecular Life Sciences, 77(15), 3027-3040. DOI: 10.1007/s00018-019-03337-5
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1007/s00018-019-03337-5
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2020
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Biochemistry & Molecular Biology,Biology,Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology,Molecular Medicine,Pharmacology
    Trkb receptors
    Transgenic mouse model
    Swimming
    Superoxide dismutase-1
    Sod1 protein, mouse
    Sod1
    Snare proteins
    Skeletal-muscle
    Skeletal muscle
    Signal transduction
    Selective vulnerability
    Protein-tyrosine kinases
    Protein kinase c-alpha
    Protein isoforms
    Polymorphism, single nucleotide
    Physical-activity
    Physical conditioning, animal
    Ntrk2 protein, mouse
    Nmj
    Neurotransmission
    Neuromuscular junction
    Muscle, skeletal
    Motor-neurons
    Motor neurons
    Motoneuron survival
    Motoneuron loss
    Mice, transgenic
    Mice
    Membrane glycoproteins
    Male
    Female
    Exercise
    Disease models, animal
    Brain-derived neurotrophic factor
    Bdnf
    Animals
    Amyotrophic lateral sclerosis
    Als
    nmj
    neurotransmission
    motoneuron loss
    exercise
    als
    Pharmacology
    Molecular medicine
    Molecular biology
    Medicina ii
    Medicina i
    General medicine
    Farmacia
    Ensino
    Educação física
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Cellular and molecular neuroscience
    Cell biology
    Biotecnología
    Biology
    Biochemistry & molecular biology
    Astronomia / física
    1420682X
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