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Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs

Chondrogenic differentiating mesenchymal stem cells (MSCs) are mimicking embryonal endochondral ossification and become hypertrophic. BMP (bone morphogenetic protein) and Activin Membrane Bound Inhibitor (BAMBI) is a pseudoreceptor that regulates the activity of transforming growth factor-β (TGF-β)...

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Autores principales: Pfeifer, Christian G., Karl, Alexandra, Berner, Arne, Zellner, Johannes, Schmitz, Paul, Loibl, Markus, Koch, Matthias, Angele, Peter, Nerlich, Michael, Mueller, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097819/
https://www.ncbi.nlm.nih.gov/pubmed/27843458
http://dx.doi.org/10.1155/2016/2685147
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author Pfeifer, Christian G.
Karl, Alexandra
Berner, Arne
Zellner, Johannes
Schmitz, Paul
Loibl, Markus
Koch, Matthias
Angele, Peter
Nerlich, Michael
Mueller, Michael B.
author_facet Pfeifer, Christian G.
Karl, Alexandra
Berner, Arne
Zellner, Johannes
Schmitz, Paul
Loibl, Markus
Koch, Matthias
Angele, Peter
Nerlich, Michael
Mueller, Michael B.
author_sort Pfeifer, Christian G.
collection PubMed
description Chondrogenic differentiating mesenchymal stem cells (MSCs) are mimicking embryonal endochondral ossification and become hypertrophic. BMP (bone morphogenetic protein) and Activin Membrane Bound Inhibitor (BAMBI) is a pseudoreceptor that regulates the activity of transforming growth factor-β (TGF-β) and BMP signalling during chondrogenesis. Both TGF-β and BMP signalling are regulators of chondrogenic cell differentiation. Human bone marrow derived MSCs were chondrogenically predifferentiated in aggregate culture for 14 days. Thereafter, one group was subjected to hypertrophy enhancing media conditions while controls were kept in chondrogenic medium until day 28. Histological evaluation, gene expression by PCR, and Western blot analysis were carried out at days 1, 3, 7, 14, 17, 21, and 28. A subset of cultures was treated with the BMP inhibitor Noggin to test for BMP dependent expression of BAMBI. Hypertrophic differentiated pellets showed larger cells with increased collagen 10 and alkaline phosphatase staining. There was significantly increased expression of BAMBI on gene expression and protein level in hypertrophic cultures compared to the chondrogenic control and increased BMP4 gene expression. Immunohistochemistry showed intense staining of BAMBI in hypertrophic cells. BAMBI expression was dose-dependently downregulated by Noggin. The pseudoreceptor BAMBI is upregulated upon enhancement of hypertrophy in MSC chondrogenic differentiation by a BMP dependent mechanism.
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spelling pubmed-50978192016-11-14 Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs Pfeifer, Christian G. Karl, Alexandra Berner, Arne Zellner, Johannes Schmitz, Paul Loibl, Markus Koch, Matthias Angele, Peter Nerlich, Michael Mueller, Michael B. Stem Cells Int Research Article Chondrogenic differentiating mesenchymal stem cells (MSCs) are mimicking embryonal endochondral ossification and become hypertrophic. BMP (bone morphogenetic protein) and Activin Membrane Bound Inhibitor (BAMBI) is a pseudoreceptor that regulates the activity of transforming growth factor-β (TGF-β) and BMP signalling during chondrogenesis. Both TGF-β and BMP signalling are regulators of chondrogenic cell differentiation. Human bone marrow derived MSCs were chondrogenically predifferentiated in aggregate culture for 14 days. Thereafter, one group was subjected to hypertrophy enhancing media conditions while controls were kept in chondrogenic medium until day 28. Histological evaluation, gene expression by PCR, and Western blot analysis were carried out at days 1, 3, 7, 14, 17, 21, and 28. A subset of cultures was treated with the BMP inhibitor Noggin to test for BMP dependent expression of BAMBI. Hypertrophic differentiated pellets showed larger cells with increased collagen 10 and alkaline phosphatase staining. There was significantly increased expression of BAMBI on gene expression and protein level in hypertrophic cultures compared to the chondrogenic control and increased BMP4 gene expression. Immunohistochemistry showed intense staining of BAMBI in hypertrophic cells. BAMBI expression was dose-dependently downregulated by Noggin. The pseudoreceptor BAMBI is upregulated upon enhancement of hypertrophy in MSC chondrogenic differentiation by a BMP dependent mechanism. Hindawi Publishing Corporation 2016 2016-10-23 /pmc/articles/PMC5097819/ /pubmed/27843458 http://dx.doi.org/10.1155/2016/2685147 Text en Copyright © 2016 Christian G. Pfeifer et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pfeifer, Christian G.
Karl, Alexandra
Berner, Arne
Zellner, Johannes
Schmitz, Paul
Loibl, Markus
Koch, Matthias
Angele, Peter
Nerlich, Michael
Mueller, Michael B.
Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title_full Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title_fullStr Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title_full_unstemmed Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title_short Expression of BMP and Actin Membrane Bound Inhibitor Is Increased during Terminal Differentiation of MSCs
title_sort expression of bmp and actin membrane bound inhibitor is increased during terminal differentiation of mscs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097819/
https://www.ncbi.nlm.nih.gov/pubmed/27843458
http://dx.doi.org/10.1155/2016/2685147
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