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The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction

The neuromuscular junction has been extensively employed in order to identify crucial determinants of synaptogenesis. At the vertebrate neuromuscular synapse, extracellular matrix and signaling proteins play stimulatory and inhibitory roles on the assembly of functional synapses. Studies in inverteb...

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Detalles Bibliográficos
Autores principales: Henríquez, Juan P., Krull, Catherine E., Osses, Nelson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257109/
https://www.ncbi.nlm.nih.gov/pubmed/22272112
http://dx.doi.org/10.3390/ijms12128924
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author Henríquez, Juan P.
Krull, Catherine E.
Osses, Nelson
author_facet Henríquez, Juan P.
Krull, Catherine E.
Osses, Nelson
author_sort Henríquez, Juan P.
collection PubMed
description The neuromuscular junction has been extensively employed in order to identify crucial determinants of synaptogenesis. At the vertebrate neuromuscular synapse, extracellular matrix and signaling proteins play stimulatory and inhibitory roles on the assembly of functional synapses. Studies in invertebrate species have revealed crucial functions of early morphogens during the assembly and maturation of the neuromuscular junction. Here, we discuss growing evidence addressing the function of Wnt and Bone morphogenetic protein (BMP) signaling pathways at the vertebrate neuromuscular synapse. We focus on the emerging role of Wnt proteins as positive and negative regulators of postsynaptic differentiation. We also address the possible involvement of BMP pathways on motor neuron behavior for the assembly and/or regeneration of the neuromuscular junction.
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spelling pubmed-32571092012-01-23 The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction Henríquez, Juan P. Krull, Catherine E. Osses, Nelson Int J Mol Sci Review The neuromuscular junction has been extensively employed in order to identify crucial determinants of synaptogenesis. At the vertebrate neuromuscular synapse, extracellular matrix and signaling proteins play stimulatory and inhibitory roles on the assembly of functional synapses. Studies in invertebrate species have revealed crucial functions of early morphogens during the assembly and maturation of the neuromuscular junction. Here, we discuss growing evidence addressing the function of Wnt and Bone morphogenetic protein (BMP) signaling pathways at the vertebrate neuromuscular synapse. We focus on the emerging role of Wnt proteins as positive and negative regulators of postsynaptic differentiation. We also address the possible involvement of BMP pathways on motor neuron behavior for the assembly and/or regeneration of the neuromuscular junction. Molecular Diversity Preservation International (MDPI) 2011-12-05 /pmc/articles/PMC3257109/ /pubmed/22272112 http://dx.doi.org/10.3390/ijms12128924 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Henríquez, Juan P.
Krull, Catherine E.
Osses, Nelson
The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title_full The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title_fullStr The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title_full_unstemmed The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title_short The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
title_sort wnt and bmp families of signaling morphogens at the vertebrate neuromuscular junction
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257109/
https://www.ncbi.nlm.nih.gov/pubmed/22272112
http://dx.doi.org/10.3390/ijms12128924
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