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...
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Published in | Scientific reports Vol. 7; no. 1; pp. 6601 - 11 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
26.07.2017
Nature Publishing Group Nature Portfolio |
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Abstract | 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. |
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AbstractList | 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. Abstract 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. Abstract 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. |
ArticleNumber | 6601 |
Author | Hau, Kwan-Leong Guillot, Pascale V. Ranzoni, Anna Maria Vlahova, Filipa David, Anna L. Hawkins, Kate De Coppi, Paolo |
Author_xml | – sequence: 1 givenname: Kwan-Leong surname: Hau fullname: Hau, Kwan-Leong organization: National Heart & Lung Institute, Hammersmith Campus, Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London – sequence: 2 givenname: Anna Maria surname: Ranzoni fullname: Ranzoni, Anna Maria organization: Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London – sequence: 3 givenname: Filipa surname: Vlahova fullname: Vlahova, Filipa organization: Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London – sequence: 4 givenname: Kate surname: Hawkins fullname: Hawkins, Kate organization: Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London – sequence: 5 givenname: Paolo surname: De Coppi fullname: De Coppi, Paolo organization: Great Ormond Street Institute of Child Health, University College London – sequence: 6 givenname: Anna L. surname: David fullname: David, Anna L. organization: Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London – sequence: 7 givenname: Pascale V. orcidid: 0000-0002-0199-6140 surname: Guillot fullname: Guillot, Pascale V. email: p.guillot@ucl.ac.uk organization: Institute for Women’s Health, Research Department of Maternal and Fetal Medicine, University College London |
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CitedBy_id | crossref_primary_10_1002_med_21796 crossref_primary_10_1002_jcp_26904 crossref_primary_10_1002_jcp_30399 crossref_primary_10_1097_CM9_0000000000002076 crossref_primary_10_1016_j_ecoenv_2018_11_064 crossref_primary_10_1007_s11302_020_09703_4 crossref_primary_10_1016_j_phrs_2019_04_007 |
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Snippet | The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells (SS-hAFSCs and... Abstract The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells... Abstract The human amniotic fluid stem cell (hAFSC) population consists of two morphologically distinct subtypes, spindle-shaped and round-shaped cells... |
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SubjectTerms | 13/100 13/106 13/31 14/63 38/39 5'-Nucleotidase - metabolism 631/532 631/532/1360 Adenosine Adenosine - metabolism Amniotic fluid Amniotic Fluid - cytology CD73 antigen Cell culture Cell Differentiation - drug effects Cell proliferation Cell Proliferation - drug effects Embryos GPI-Linked Proteins - metabolism Humanities and Social Sciences Humans Mesenchyme multidisciplinary Osteogenesis Science Science (multidisciplinary) Stem cells Stem Cells - drug effects Therapeutic applications Transforming Growth Factor beta - metabolism |
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Title | TGFβ-induced osteogenic potential of human amniotic fluid stem cells via CD73-generated adenosine production |
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