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The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro
Chronic systemic inflammation is a clinical symptom in children with cystic fibrosis (CF), but the effects on skeletal muscle development are unknown. The aims of this study were to determine (1) the effects of systemic factors from children with CF and healthy controls on myoblast proliferation, an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208655/ https://www.ncbi.nlm.nih.gov/pubmed/24944290 http://dx.doi.org/10.14814/phy2.12042 |
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author | Nguyen, Thanh Baker, Jeff M. Obeid, Joyce Raha, Sandeep Parise, Gianni Pedder, Linda Timmons, Brian W. |
author_facet | Nguyen, Thanh Baker, Jeff M. Obeid, Joyce Raha, Sandeep Parise, Gianni Pedder, Linda Timmons, Brian W. |
author_sort | Nguyen, Thanh |
collection | PubMed |
description | Chronic systemic inflammation is a clinical symptom in children with cystic fibrosis (CF), but the effects on skeletal muscle development are unknown. The aims of this study were to determine (1) the effects of systemic factors from children with CF and healthy controls on myoblast proliferation, and (2) whether exercise serum can have an effect on proliferation in vitro. Eleven children with CF and 11 biological age‐matched controls completed two 30‐min bouts of cycling at an intensity set at 50% peak mechanical power. Serum samples were collected before exercise (REST), immediately following exercise (EX), and after 60 min of recovery (REC). Serum samples prepared in group‐specific pools were used for cell culture experiments. C2C12 myoblasts were incubated in 5% serum and media for 1 h and then immediately harvested for protein and mRNA analysis, or incubated in growth media for 2 days to examine proliferation. C2C12 myoblasts treated with CF serum displayed greater proliferation phenotype than myoblasts treated with control serum. Proliferation did not change with EX or REC serum from children with CF compared to CF REST serum, while proliferation was increased with EX and REC serum from control compared to control REST serum. These findings suggest that systemic factors from children with CF at rest and after exercise can alter myoblast proliferation responses when compared to systemic factors from healthy children, which may have implications on skeletal muscle development. |
format | Online Article Text |
id | pubmed-4208655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Wiley Periodicals, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42086552014-11-25 The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro Nguyen, Thanh Baker, Jeff M. Obeid, Joyce Raha, Sandeep Parise, Gianni Pedder, Linda Timmons, Brian W. Physiol Rep Original Research Chronic systemic inflammation is a clinical symptom in children with cystic fibrosis (CF), but the effects on skeletal muscle development are unknown. The aims of this study were to determine (1) the effects of systemic factors from children with CF and healthy controls on myoblast proliferation, and (2) whether exercise serum can have an effect on proliferation in vitro. Eleven children with CF and 11 biological age‐matched controls completed two 30‐min bouts of cycling at an intensity set at 50% peak mechanical power. Serum samples were collected before exercise (REST), immediately following exercise (EX), and after 60 min of recovery (REC). Serum samples prepared in group‐specific pools were used for cell culture experiments. C2C12 myoblasts were incubated in 5% serum and media for 1 h and then immediately harvested for protein and mRNA analysis, or incubated in growth media for 2 days to examine proliferation. C2C12 myoblasts treated with CF serum displayed greater proliferation phenotype than myoblasts treated with control serum. Proliferation did not change with EX or REC serum from children with CF compared to CF REST serum, while proliferation was increased with EX and REC serum from control compared to control REST serum. These findings suggest that systemic factors from children with CF at rest and after exercise can alter myoblast proliferation responses when compared to systemic factors from healthy children, which may have implications on skeletal muscle development. Wiley Periodicals, Inc. 2014-06-24 /pmc/articles/PMC4208655/ /pubmed/24944290 http://dx.doi.org/10.14814/phy2.12042 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Nguyen, Thanh Baker, Jeff M. Obeid, Joyce Raha, Sandeep Parise, Gianni Pedder, Linda Timmons, Brian W. The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title | The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title_full | The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title_fullStr | The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title_full_unstemmed | The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title_short | The effects of resting and exercise serum from children with cystic fibrosis on C2C12 myoblast proliferation in vitro |
title_sort | effects of resting and exercise serum from children with cystic fibrosis on c2c12 myoblast proliferation in vitro |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208655/ https://www.ncbi.nlm.nih.gov/pubmed/24944290 http://dx.doi.org/10.14814/phy2.12042 |
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