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Plum modulates Myoglianin and regulates synaptic function in D. melanogaster

Alterations in the neuromuscular system underlie several neuromuscular diseases and play critical roles in the development of sarcopenia, the age-related loss of muscle mass and function. Mammalian Myostatin (MST) and GDF11, members of the TGF-β superfamily of growth factors, are powerful regulators...

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Autores principales: Sahota, Virender K., Stone, Aelfwin, Woodling, Nathaniel S., Spiers, Jereme G., Steinert, Joern R., Partridge, Linda, Augustin, Hrvoje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497343/
https://www.ncbi.nlm.nih.gov/pubmed/37699519
http://dx.doi.org/10.1098/rsob.230171
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author Sahota, Virender K.
Stone, Aelfwin
Woodling, Nathaniel S.
Spiers, Jereme G.
Steinert, Joern R.
Partridge, Linda
Augustin, Hrvoje
author_facet Sahota, Virender K.
Stone, Aelfwin
Woodling, Nathaniel S.
Spiers, Jereme G.
Steinert, Joern R.
Partridge, Linda
Augustin, Hrvoje
author_sort Sahota, Virender K.
collection PubMed
description Alterations in the neuromuscular system underlie several neuromuscular diseases and play critical roles in the development of sarcopenia, the age-related loss of muscle mass and function. Mammalian Myostatin (MST) and GDF11, members of the TGF-β superfamily of growth factors, are powerful regulators of muscle size in both model organisms and humans. Myoglianin (MYO), the Drosophila homologue of MST and GDF11, is a strong inhibitor of synaptic function and structure at the neuromuscular junction in flies. Here, we identified Plum, a transmembrane cell surface protein, as a modulator of MYO function in the larval neuromuscular system. Reduction of Plum in the larval body-wall muscles abolishes the previously demonstrated positive effect of attenuated MYO signalling on both muscle size and neuromuscular junction structure and function. In addition, downregulation of Plum on its own results in decreased synaptic strength and body weight, classifying Plum as a (novel) regulator of neuromuscular function and body (muscle) size. These findings offer new insights into possible regulatory mechanisms behind ageing- and disease-related neuromuscular dysfunctions in humans and identify potential targets for therapeutic interventions.
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spelling pubmed-104973432023-09-13 Plum modulates Myoglianin and regulates synaptic function in D. melanogaster Sahota, Virender K. Stone, Aelfwin Woodling, Nathaniel S. Spiers, Jereme G. Steinert, Joern R. Partridge, Linda Augustin, Hrvoje Open Biol Research Alterations in the neuromuscular system underlie several neuromuscular diseases and play critical roles in the development of sarcopenia, the age-related loss of muscle mass and function. Mammalian Myostatin (MST) and GDF11, members of the TGF-β superfamily of growth factors, are powerful regulators of muscle size in both model organisms and humans. Myoglianin (MYO), the Drosophila homologue of MST and GDF11, is a strong inhibitor of synaptic function and structure at the neuromuscular junction in flies. Here, we identified Plum, a transmembrane cell surface protein, as a modulator of MYO function in the larval neuromuscular system. Reduction of Plum in the larval body-wall muscles abolishes the previously demonstrated positive effect of attenuated MYO signalling on both muscle size and neuromuscular junction structure and function. In addition, downregulation of Plum on its own results in decreased synaptic strength and body weight, classifying Plum as a (novel) regulator of neuromuscular function and body (muscle) size. These findings offer new insights into possible regulatory mechanisms behind ageing- and disease-related neuromuscular dysfunctions in humans and identify potential targets for therapeutic interventions. The Royal Society 2023-09-13 /pmc/articles/PMC10497343/ /pubmed/37699519 http://dx.doi.org/10.1098/rsob.230171 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Sahota, Virender K.
Stone, Aelfwin
Woodling, Nathaniel S.
Spiers, Jereme G.
Steinert, Joern R.
Partridge, Linda
Augustin, Hrvoje
Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title_full Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title_fullStr Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title_full_unstemmed Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title_short Plum modulates Myoglianin and regulates synaptic function in D. melanogaster
title_sort plum modulates myoglianin and regulates synaptic function in d. melanogaster
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497343/
https://www.ncbi.nlm.nih.gov/pubmed/37699519
http://dx.doi.org/10.1098/rsob.230171
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