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Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation
Regeneration of muscle fibers that are lost during pathological muscle degeneration or after injuries is sustained by the production of new myofibers. An important cell type involved in muscle regeneration is the satellite cell. Necdin is a protein expressed in satellite cell–derived myogenic precur...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064766/ https://www.ncbi.nlm.nih.gov/pubmed/17954612 http://dx.doi.org/10.1083/jcb.200701027 |
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author | Deponti, Daniela François, Stéphanie Baesso, Silvia Sciorati, Clara Innocenzi, Anna Broccoli, Vania Muscatelli, Françoise Meneveri, Raffaella Clementi, Emilio Cossu, Giulio Brunelli, Silvia |
author_facet | Deponti, Daniela François, Stéphanie Baesso, Silvia Sciorati, Clara Innocenzi, Anna Broccoli, Vania Muscatelli, Françoise Meneveri, Raffaella Clementi, Emilio Cossu, Giulio Brunelli, Silvia |
author_sort | Deponti, Daniela |
collection | PubMed |
description | Regeneration of muscle fibers that are lost during pathological muscle degeneration or after injuries is sustained by the production of new myofibers. An important cell type involved in muscle regeneration is the satellite cell. Necdin is a protein expressed in satellite cell–derived myogenic precursors during perinatal growth. However, its function in myogenesis is not known. We compare transgenic mice that overexpress necdin in skeletal muscle with both wild-type and necdin null mice. After muscle injury the necdin null mice show a considerable defect in muscle healing, whereas mice that overexpress necdin show a substantial increase in myofiber regeneration. We also find that in muscle, necdin increases myogenin expression, accelerates differentiation, and counteracts myoblast apoptosis. Collectively, these data clarify the function and mechanism of necdin in skeletal muscle and show the importance of necdin in muscle regeneration. |
format | Text |
id | pubmed-2064766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20647662008-04-22 Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation Deponti, Daniela François, Stéphanie Baesso, Silvia Sciorati, Clara Innocenzi, Anna Broccoli, Vania Muscatelli, Françoise Meneveri, Raffaella Clementi, Emilio Cossu, Giulio Brunelli, Silvia J Cell Biol Research Articles Regeneration of muscle fibers that are lost during pathological muscle degeneration or after injuries is sustained by the production of new myofibers. An important cell type involved in muscle regeneration is the satellite cell. Necdin is a protein expressed in satellite cell–derived myogenic precursors during perinatal growth. However, its function in myogenesis is not known. We compare transgenic mice that overexpress necdin in skeletal muscle with both wild-type and necdin null mice. After muscle injury the necdin null mice show a considerable defect in muscle healing, whereas mice that overexpress necdin show a substantial increase in myofiber regeneration. We also find that in muscle, necdin increases myogenin expression, accelerates differentiation, and counteracts myoblast apoptosis. Collectively, these data clarify the function and mechanism of necdin in skeletal muscle and show the importance of necdin in muscle regeneration. The Rockefeller University Press 2007-10-22 /pmc/articles/PMC2064766/ /pubmed/17954612 http://dx.doi.org/10.1083/jcb.200701027 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Deponti, Daniela François, Stéphanie Baesso, Silvia Sciorati, Clara Innocenzi, Anna Broccoli, Vania Muscatelli, Françoise Meneveri, Raffaella Clementi, Emilio Cossu, Giulio Brunelli, Silvia Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title | Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title_full | Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title_fullStr | Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title_full_unstemmed | Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title_short | Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
title_sort | necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064766/ https://www.ncbi.nlm.nih.gov/pubmed/17954612 http://dx.doi.org/10.1083/jcb.200701027 |
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