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Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro

Salinomycin is a polyether antiprotozoal antibiotic that is used as a food additive, particularly in poultry farming. By consuming animal products, there may be a chronic human exposure to salinomycin. Salinomycin inhibits the differentiation of preadipocytes into adipocytes. As human mesenchymal st...

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Detalles Bibliográficos
Autores principales: SCHERZAD, AGMAL, HACKENBERG, STEPHAN, FROELICH, KATRIN, RAK, KRISTEN, HAGEN, RUDOLF, TAEGER, JOHANNES, BREGENZER, MAXIMILLIAN, KLEINSASSER, NORBERT
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774322/
https://www.ncbi.nlm.nih.gov/pubmed/26998269
http://dx.doi.org/10.3892/br.2016.572
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author SCHERZAD, AGMAL
HACKENBERG, STEPHAN
FROELICH, KATRIN
RAK, KRISTEN
HAGEN, RUDOLF
TAEGER, JOHANNES
BREGENZER, MAXIMILLIAN
KLEINSASSER, NORBERT
author_facet SCHERZAD, AGMAL
HACKENBERG, STEPHAN
FROELICH, KATRIN
RAK, KRISTEN
HAGEN, RUDOLF
TAEGER, JOHANNES
BREGENZER, MAXIMILLIAN
KLEINSASSER, NORBERT
author_sort SCHERZAD, AGMAL
collection PubMed
description Salinomycin is a polyether antiprotozoal antibiotic that is used as a food additive, particularly in poultry farming. By consuming animal products, there may be a chronic human exposure to salinomycin. Salinomycin inhibits the differentiation of preadipocytes into adipocytes. As human mesenchymal stem cells (MSC) may differentiate into different mesenchymal cells, it thus appeared worthwhile to investigate whether chronic salinomycin exposure impairs the functional properties of MSC and induces genotoxic effects. Bone marrow MSC were treated with low-dose salinomycin (100 nM) (MSC-Sal) for 4 weeks, while the medium containing salinomycin was changed every other day. Functional changes were evaluated and compared to MSC without salinomycin treatment (MSC-control). MSC-Sal and MSC-control were positive for cluster of differentiation 90 (CD90), CD73 and CD44, and negative for CD34. There were no differences observed in cell morphology or cytoskeletal structures following salinomycin exposure. The differentiation into adipocytes and osteocytes was not counteracted by salinomycin, and proliferation capability was not inhibited following salinomycin exposure. The migration of MSC-Sal was attenuated significantly as compared to the MSC-control. There were no genotoxic effects after 4 weeks of salinomycin exposure. The present study shows an altered migration capacity as a sign of functional impairment of MSC induced by chronic salinomycin exposure. Further in vitro toxicological investigations, particularly with primary human cells, are required to understand the impact of chronic salinomycin consumption on human cell systems.
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spelling pubmed-47743222016-03-18 Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro SCHERZAD, AGMAL HACKENBERG, STEPHAN FROELICH, KATRIN RAK, KRISTEN HAGEN, RUDOLF TAEGER, JOHANNES BREGENZER, MAXIMILLIAN KLEINSASSER, NORBERT Biomed Rep Articles Salinomycin is a polyether antiprotozoal antibiotic that is used as a food additive, particularly in poultry farming. By consuming animal products, there may be a chronic human exposure to salinomycin. Salinomycin inhibits the differentiation of preadipocytes into adipocytes. As human mesenchymal stem cells (MSC) may differentiate into different mesenchymal cells, it thus appeared worthwhile to investigate whether chronic salinomycin exposure impairs the functional properties of MSC and induces genotoxic effects. Bone marrow MSC were treated with low-dose salinomycin (100 nM) (MSC-Sal) for 4 weeks, while the medium containing salinomycin was changed every other day. Functional changes were evaluated and compared to MSC without salinomycin treatment (MSC-control). MSC-Sal and MSC-control were positive for cluster of differentiation 90 (CD90), CD73 and CD44, and negative for CD34. There were no differences observed in cell morphology or cytoskeletal structures following salinomycin exposure. The differentiation into adipocytes and osteocytes was not counteracted by salinomycin, and proliferation capability was not inhibited following salinomycin exposure. The migration of MSC-Sal was attenuated significantly as compared to the MSC-control. There were no genotoxic effects after 4 weeks of salinomycin exposure. The present study shows an altered migration capacity as a sign of functional impairment of MSC induced by chronic salinomycin exposure. Further in vitro toxicological investigations, particularly with primary human cells, are required to understand the impact of chronic salinomycin consumption on human cell systems. D.A. Spandidos 2016-03 2016-01-14 /pmc/articles/PMC4774322/ /pubmed/26998269 http://dx.doi.org/10.3892/br.2016.572 Text en Copyright: © Scherzad et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
SCHERZAD, AGMAL
HACKENBERG, STEPHAN
FROELICH, KATRIN
RAK, KRISTEN
HAGEN, RUDOLF
TAEGER, JOHANNES
BREGENZER, MAXIMILLIAN
KLEINSASSER, NORBERT
Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title_full Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title_fullStr Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title_full_unstemmed Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title_short Chronic exposure of low dose salinomycin inhibits MSC migration capability in vitro
title_sort chronic exposure of low dose salinomycin inhibits msc migration capability in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774322/
https://www.ncbi.nlm.nih.gov/pubmed/26998269
http://dx.doi.org/10.3892/br.2016.572
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