Cargando…

Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15

INTRODUCTION: Type 1 interferon (IFN)-inducible genes and their inducible products are upregulated in dermatomyositis muscle. Of these, IFN-stimulated gene 15 (ISG15) is one of the most upregulated, suggesting its possible involvement in the pathogenesis of this disease. To test this postulate, we d...

Descripción completa

Detalles Bibliográficos
Autores principales: Franzi, Sara, Salajegheh, Mohammad, Nazareno, Remedios, Greenberg, Steven A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672209/
https://www.ncbi.nlm.nih.gov/pubmed/23750257
http://dx.doi.org/10.1371/journal.pone.0065362
_version_ 1782272095029297152
author Franzi, Sara
Salajegheh, Mohammad
Nazareno, Remedios
Greenberg, Steven A.
author_facet Franzi, Sara
Salajegheh, Mohammad
Nazareno, Remedios
Greenberg, Steven A.
author_sort Franzi, Sara
collection PubMed
description INTRODUCTION: Type 1 interferon (IFN)-inducible genes and their inducible products are upregulated in dermatomyositis muscle. Of these, IFN-stimulated gene 15 (ISG15) is one of the most upregulated, suggesting its possible involvement in the pathogenesis of this disease. To test this postulate, we developed a model of type 1 IFN mediated myotube toxicity and assessed whether or not downregulation of ISG15 expression prevents this toxicity. METHODS: Mouse myoblasts (C2C12 cell line) were cultured in the presence of type 1 or type 2 IFNs and ISG15 expression assessed by microarray analysis. The morphology of newly formed myotubes was assessed by measuring their length, diameter, and area on micrographs using imaging software. ISG15 expression was silenced through transfection with small interference RNA. RESULTS: Type 1 IFNs, especially IFN-beta, increased ISG15 expression in C2C12 cells and impaired myotube formation. Silencing of ISG15 resulted in knockdown of ISG15 protein, but without phenotypic rescue of myotube formation. DISCUSSION: IFN-beta affects myoblast differentiation ability and myotube morphology in vitro.These studies provide evidence that ISG15, which is highly upregulated in dermatomyositis muscle, does not appear to play a key role in IFN-beta-mediated C2C12 myoblast cell fusion.
format Online
Article
Text
id pubmed-3672209
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36722092013-06-07 Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15 Franzi, Sara Salajegheh, Mohammad Nazareno, Remedios Greenberg, Steven A. PLoS One Research Article INTRODUCTION: Type 1 interferon (IFN)-inducible genes and their inducible products are upregulated in dermatomyositis muscle. Of these, IFN-stimulated gene 15 (ISG15) is one of the most upregulated, suggesting its possible involvement in the pathogenesis of this disease. To test this postulate, we developed a model of type 1 IFN mediated myotube toxicity and assessed whether or not downregulation of ISG15 expression prevents this toxicity. METHODS: Mouse myoblasts (C2C12 cell line) were cultured in the presence of type 1 or type 2 IFNs and ISG15 expression assessed by microarray analysis. The morphology of newly formed myotubes was assessed by measuring their length, diameter, and area on micrographs using imaging software. ISG15 expression was silenced through transfection with small interference RNA. RESULTS: Type 1 IFNs, especially IFN-beta, increased ISG15 expression in C2C12 cells and impaired myotube formation. Silencing of ISG15 resulted in knockdown of ISG15 protein, but without phenotypic rescue of myotube formation. DISCUSSION: IFN-beta affects myoblast differentiation ability and myotube morphology in vitro.These studies provide evidence that ISG15, which is highly upregulated in dermatomyositis muscle, does not appear to play a key role in IFN-beta-mediated C2C12 myoblast cell fusion. Public Library of Science 2013-06-04 /pmc/articles/PMC3672209/ /pubmed/23750257 http://dx.doi.org/10.1371/journal.pone.0065362 Text en © 2013 Franzi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Franzi, Sara
Salajegheh, Mohammad
Nazareno, Remedios
Greenberg, Steven A.
Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title_full Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title_fullStr Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title_full_unstemmed Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title_short Type 1 Interferons Inhibit Myotube Formation Independently of Upregulation of Interferon-Stimulated Gene 15
title_sort type 1 interferons inhibit myotube formation independently of upregulation of interferon-stimulated gene 15
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672209/
https://www.ncbi.nlm.nih.gov/pubmed/23750257
http://dx.doi.org/10.1371/journal.pone.0065362
work_keys_str_mv AT franzisara type1interferonsinhibitmyotubeformationindependentlyofupregulationofinterferonstimulatedgene15
AT salajeghehmohammad type1interferonsinhibitmyotubeformationindependentlyofupregulationofinterferonstimulatedgene15
AT nazarenoremedios type1interferonsinhibitmyotubeformationindependentlyofupregulationofinterferonstimulatedgene15
AT greenbergstevena type1interferonsinhibitmyotubeformationindependentlyofupregulationofinterferonstimulatedgene15