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Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells

Alternan, an α-1,3- and α-1,6-linked glucan, is a polysaccharide that is produced by bacteria. Although the structure of alternan used in this study, an α-1,3- and α-1,6-linked glucan (hereafter referred to as alternan), has been comprehensively characterized, its function on cell biology, especiall...

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Autores principales: Charoenwongpaiboon, Thanapon, Supraditaporn, Kantpitchar, Klaimon, Phatchanat, Wangpaiboon, Karan, Pichyangkura, Rath, Issaragrisil, Surapol, Lorthongpanich, Chanchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060545/
https://www.ncbi.nlm.nih.gov/pubmed/35520166
http://dx.doi.org/10.1039/c8ra10263e
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author Charoenwongpaiboon, Thanapon
Supraditaporn, Kantpitchar
Klaimon, Phatchanat
Wangpaiboon, Karan
Pichyangkura, Rath
Issaragrisil, Surapol
Lorthongpanich, Chanchao
author_facet Charoenwongpaiboon, Thanapon
Supraditaporn, Kantpitchar
Klaimon, Phatchanat
Wangpaiboon, Karan
Pichyangkura, Rath
Issaragrisil, Surapol
Lorthongpanich, Chanchao
author_sort Charoenwongpaiboon, Thanapon
collection PubMed
description Alternan, an α-1,3- and α-1,6-linked glucan, is a polysaccharide that is produced by bacteria. Although the structure of alternan used in this study, an α-1,3- and α-1,6-linked glucan (hereafter referred to as alternan), has been comprehensively characterized, its function on cell biology, especially relative to cell growth and differentiation, has not been fully elucidated. In this study, we set forth to compare the effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells (MSCs). The effect of chitosan on MSC differentiation has already been well characterized. The treated cells were determined for cell proliferation and differentiation capacity compared to untreated cells. The result showed that treatment by alternan or chitosan increased cell proliferation, as demonstrated by increased cell number and scratched regions that were fully restored in less time than it took to fully restore controls. Further investigation found that alternan and chitosan activates the toll-like receptor (TLR) pathway suggesting that these cells may be prone to differentiation. In agreement with this result, an increase in deposited calcium was observed in alternan- or chitosan-treated cells after osteogenic differentiation induction. However, adipogenic differentiation was significantly inhibited in the presence of chitosan, but no change was observed in alternan treatment. Taken together, these results demonstrate biological effects of alternan on human MSCs. Moreover, these novel roles of alternan may have important beneficial medical applications and may provide a basis from which stem cell therapies can be developed in the future.
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spelling pubmed-90605452022-05-04 Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells Charoenwongpaiboon, Thanapon Supraditaporn, Kantpitchar Klaimon, Phatchanat Wangpaiboon, Karan Pichyangkura, Rath Issaragrisil, Surapol Lorthongpanich, Chanchao RSC Adv Chemistry Alternan, an α-1,3- and α-1,6-linked glucan, is a polysaccharide that is produced by bacteria. Although the structure of alternan used in this study, an α-1,3- and α-1,6-linked glucan (hereafter referred to as alternan), has been comprehensively characterized, its function on cell biology, especially relative to cell growth and differentiation, has not been fully elucidated. In this study, we set forth to compare the effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells (MSCs). The effect of chitosan on MSC differentiation has already been well characterized. The treated cells were determined for cell proliferation and differentiation capacity compared to untreated cells. The result showed that treatment by alternan or chitosan increased cell proliferation, as demonstrated by increased cell number and scratched regions that were fully restored in less time than it took to fully restore controls. Further investigation found that alternan and chitosan activates the toll-like receptor (TLR) pathway suggesting that these cells may be prone to differentiation. In agreement with this result, an increase in deposited calcium was observed in alternan- or chitosan-treated cells after osteogenic differentiation induction. However, adipogenic differentiation was significantly inhibited in the presence of chitosan, but no change was observed in alternan treatment. Taken together, these results demonstrate biological effects of alternan on human MSCs. Moreover, these novel roles of alternan may have important beneficial medical applications and may provide a basis from which stem cell therapies can be developed in the future. The Royal Society of Chemistry 2019-02-04 /pmc/articles/PMC9060545/ /pubmed/35520166 http://dx.doi.org/10.1039/c8ra10263e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Charoenwongpaiboon, Thanapon
Supraditaporn, Kantpitchar
Klaimon, Phatchanat
Wangpaiboon, Karan
Pichyangkura, Rath
Issaragrisil, Surapol
Lorthongpanich, Chanchao
Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title_full Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title_fullStr Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title_full_unstemmed Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title_short Effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
title_sort effect of alternan versus chitosan on the biological properties of human mesenchymal stem cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060545/
https://www.ncbi.nlm.nih.gov/pubmed/35520166
http://dx.doi.org/10.1039/c8ra10263e
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