Cargando…

TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production

The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells (SS-hAFSCs and RS-hAFSCs). Whilst SS-hAFSCs are routinely expanded in mesenchymal-type (MT) conditions, we previously showed that they acquire broader differ...

Descripción completa

Detalles Bibliográficos
Autores principales: Hau, Kwan-Leong, Ranzoni, Anna Maria, Vlahova, Filipa, Hawkins, Kate, De Coppi, Paolo, David, Anna L., Guillot, Pascale V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529586/
https://www.ncbi.nlm.nih.gov/pubmed/28747757
http://dx.doi.org/10.1038/s41598-017-06780-1
_version_ 1783253156776378368
author Hau, Kwan-Leong
Ranzoni, Anna Maria
Vlahova, Filipa
Hawkins, Kate
De Coppi, Paolo
David, Anna L.
Guillot, Pascale V.
author_facet Hau, Kwan-Leong
Ranzoni, Anna Maria
Vlahova, Filipa
Hawkins, Kate
De Coppi, Paolo
David, Anna L.
Guillot, Pascale V.
author_sort Hau, Kwan-Leong
collection PubMed
description The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells (SS-hAFSCs and RS-hAFSCs). Whilst SS-hAFSCs are routinely expanded in mesenchymal-type (MT) conditions, we previously showed that they acquire broader differentiation potential when cultured under embryonic-type (ET) conditions. However, the effects of culture conditions on RS-hAFSCs have not been determined. Here, we show that culturing RS-hAFSCs under ET conditions confers faster proliferation and enhances the efficiency of osteogenic differentiation of the cells. We show that this occurs via TGFβ-induced activation of CD73 and the associated increase in the generation of extracellular adenosine. Our data demonstrate that culture conditions are decisive for the expansion of hAFSCs and that TGFβ present in ET conditions causes the phenotype of RS-hAFSCs to revert to an earlier state of stemness. Cultivating RS-hAFSCs in ET conditions with TGFβ may therefore increase their therapeutic potential for clinical applications.
format Online
Article
Text
id pubmed-5529586
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55295862017-08-02 TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production Hau, Kwan-Leong Ranzoni, Anna Maria Vlahova, Filipa Hawkins, Kate De Coppi, Paolo David, Anna L. Guillot, Pascale V. Sci Rep Article The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells (SS-hAFSCs and RS-hAFSCs). Whilst SS-hAFSCs are routinely expanded in mesenchymal-type (MT) conditions, we previously showed that they acquire broader differentiation potential when cultured under embryonic-type (ET) conditions. However, the effects of culture conditions on RS-hAFSCs have not been determined. Here, we show that culturing RS-hAFSCs under ET conditions confers faster proliferation and enhances the efficiency of osteogenic differentiation of the cells. We show that this occurs via TGFβ-induced activation of CD73 and the associated increase in the generation of extracellular adenosine. Our data demonstrate that culture conditions are decisive for the expansion of hAFSCs and that TGFβ present in ET conditions causes the phenotype of RS-hAFSCs to revert to an earlier state of stemness. Cultivating RS-hAFSCs in ET conditions with TGFβ may therefore increase their therapeutic potential for clinical applications. Nature Publishing Group UK 2017-07-26 /pmc/articles/PMC5529586/ /pubmed/28747757 http://dx.doi.org/10.1038/s41598-017-06780-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hau, Kwan-Leong
Ranzoni, Anna Maria
Vlahova, Filipa
Hawkins, Kate
De Coppi, Paolo
David, Anna L.
Guillot, Pascale V.
TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title_full TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title_fullStr TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title_full_unstemmed TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title_short TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production
title_sort tgfβ-induced osteogenic potential of human amniotic fluid stem cells via cd73-generated adenosine production
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529586/
https://www.ncbi.nlm.nih.gov/pubmed/28747757
http://dx.doi.org/10.1038/s41598-017-06780-1
work_keys_str_mv AT haukwanleong tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT ranzoniannamaria tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT vlahovafilipa tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT hawkinskate tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT decoppipaolo tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT davidannal tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction
AT guillotpascalev tgfbinducedosteogenicpotentialofhumanamnioticfluidstemcellsviacd73generatedadenosineproduction