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Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis
We recently identified osmolyte accumulators as novel biomarkers for chronic skeletal muscle inflammation and weakness, but their precise involvement in inflammatory myopathies remains elusive. In the current study, we demonstrate in vitro that, in myoblasts and myotubes exposed to pro-inflammatory...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193116/ https://www.ncbi.nlm.nih.gov/pubmed/30364257 http://dx.doi.org/10.3389/fneur.2018.00846 |
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author | De Paepe, Boel Zschüntzsch, Jana Šokčević, Tea Weis, Joachim Schmidt, Jens De Bleecker, Jan L. |
author_facet | De Paepe, Boel Zschüntzsch, Jana Šokčević, Tea Weis, Joachim Schmidt, Jens De Bleecker, Jan L. |
author_sort | De Paepe, Boel |
collection | PubMed |
description | We recently identified osmolyte accumulators as novel biomarkers for chronic skeletal muscle inflammation and weakness, but their precise involvement in inflammatory myopathies remains elusive. In the current study, we demonstrate in vitro that, in myoblasts and myotubes exposed to pro-inflammatory cytokines or increased salt concentration, mRNA levels of the osmolyte carriers SLC5A3, SLC6A6, SLC6A12, and AKR1B1 enzyme can be upregulated. Induction of SLC6A12 and AKR1B1 was confirmed at the protein level using immunofluorescence and Western blotting. Gene silencing by specific siRNAs revealed that these factors were vital for muscle cells under hyperosmotic conditions. Pro-inflammatory cytokines activated mitogen-activated protein kinases, nuclear factor κB as well as nuclear factor of activated T-cells 5 mRNA expression. In muscle biopsies from patients with polymyositis or sporadic inclusion body myositis, osmolyte pathway activation was observed in regenerating muscle fibers. In addition, the osmolyte carriers SLC5A3 and SLC6A12 localized to subsets of immune cells, most notably to the endomysial macrophages and T-cells. Collectively, this study unveiled that muscle cells respond to osmotic and inflammatory stress by osmolyte pathway activation, likely orchestrating general protection of the tissue. Moreover, pro-inflammatory properties are attributed to SLC5A3 and SLC6A12 in auto-aggressive macrophages and T-cells in inflamed skeletal muscle. |
format | Online Article Text |
id | pubmed-6193116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61931162018-10-25 Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis De Paepe, Boel Zschüntzsch, Jana Šokčević, Tea Weis, Joachim Schmidt, Jens De Bleecker, Jan L. Front Neurol Neurology We recently identified osmolyte accumulators as novel biomarkers for chronic skeletal muscle inflammation and weakness, but their precise involvement in inflammatory myopathies remains elusive. In the current study, we demonstrate in vitro that, in myoblasts and myotubes exposed to pro-inflammatory cytokines or increased salt concentration, mRNA levels of the osmolyte carriers SLC5A3, SLC6A6, SLC6A12, and AKR1B1 enzyme can be upregulated. Induction of SLC6A12 and AKR1B1 was confirmed at the protein level using immunofluorescence and Western blotting. Gene silencing by specific siRNAs revealed that these factors were vital for muscle cells under hyperosmotic conditions. Pro-inflammatory cytokines activated mitogen-activated protein kinases, nuclear factor κB as well as nuclear factor of activated T-cells 5 mRNA expression. In muscle biopsies from patients with polymyositis or sporadic inclusion body myositis, osmolyte pathway activation was observed in regenerating muscle fibers. In addition, the osmolyte carriers SLC5A3 and SLC6A12 localized to subsets of immune cells, most notably to the endomysial macrophages and T-cells. Collectively, this study unveiled that muscle cells respond to osmotic and inflammatory stress by osmolyte pathway activation, likely orchestrating general protection of the tissue. Moreover, pro-inflammatory properties are attributed to SLC5A3 and SLC6A12 in auto-aggressive macrophages and T-cells in inflamed skeletal muscle. Frontiers Media S.A. 2018-10-11 /pmc/articles/PMC6193116/ /pubmed/30364257 http://dx.doi.org/10.3389/fneur.2018.00846 Text en Copyright © 2018 De Paepe, Zschüntzsch, Šokčević, Weis, Schmidt and De Bleecker. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology De Paepe, Boel Zschüntzsch, Jana Šokčević, Tea Weis, Joachim Schmidt, Jens De Bleecker, Jan L. Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title | Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title_full | Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title_fullStr | Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title_full_unstemmed | Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title_short | Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis |
title_sort | induction of osmolyte pathways in skeletal muscle inflammation: novel biomarkers for myositis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193116/ https://www.ncbi.nlm.nih.gov/pubmed/30364257 http://dx.doi.org/10.3389/fneur.2018.00846 |
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