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Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation

Signals from the microenvironment around a cell are known to influence cell behavior. Material properties, such as biochemical composition and substrate stiffness, are today accepted as significant regulators of stem cell fate. The knowledge of how cell behavior is influenced by 3D geometric cues is...

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Autores principales: Werner, Maike, Blanquer, Sébastien B. G., Haimi, Suvi P., Korus, Gabriela, Dunlop, John W. C., Duda, Georg N., Grijpma, Dirk. W., Petersen, Ansgar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323878/
https://www.ncbi.nlm.nih.gov/pubmed/28251054
http://dx.doi.org/10.1002/advs.201600347
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author Werner, Maike
Blanquer, Sébastien B. G.
Haimi, Suvi P.
Korus, Gabriela
Dunlop, John W. C.
Duda, Georg N.
Grijpma, Dirk. W.
Petersen, Ansgar
author_facet Werner, Maike
Blanquer, Sébastien B. G.
Haimi, Suvi P.
Korus, Gabriela
Dunlop, John W. C.
Duda, Georg N.
Grijpma, Dirk. W.
Petersen, Ansgar
author_sort Werner, Maike
collection PubMed
description Signals from the microenvironment around a cell are known to influence cell behavior. Material properties, such as biochemical composition and substrate stiffness, are today accepted as significant regulators of stem cell fate. The knowledge of how cell behavior is influenced by 3D geometric cues is, however, strongly limited despite its potential relevance for the understanding of tissue regenerative processes and the design of biomaterials. Here, the role of surface curvature on the migratory and differentiation behavior of human mesenchymal stem cells (hMSCs) has been investigated on 3D surfaces with well‐defined geometric features produced by stereolithography. Time lapse microscopy reveals a significant increase of cell migration speed on concave spherical compared to convex spherical structures and flat surfaces resulting from an upward‐lift of the cell body due to cytoskeletal forces. On convex surfaces, cytoskeletal forces lead to substantial nuclear deformation, increase lamin‐A levels and promote osteogenic differentiation. The findings of this study demonstrate a so far missing link between 3D surface curvature and hMSC behavior. This will not only help to better understand the role of extracellular matrix architecture in health and disease but also give new insights in how 3D geometries can be used as a cell‐instructive material parameter in the field of biomaterial‐guided tissue regeneration.
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spelling pubmed-53238782017-03-01 Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation Werner, Maike Blanquer, Sébastien B. G. Haimi, Suvi P. Korus, Gabriela Dunlop, John W. C. Duda, Georg N. Grijpma, Dirk. W. Petersen, Ansgar Adv Sci (Weinh) Full Papers Signals from the microenvironment around a cell are known to influence cell behavior. Material properties, such as biochemical composition and substrate stiffness, are today accepted as significant regulators of stem cell fate. The knowledge of how cell behavior is influenced by 3D geometric cues is, however, strongly limited despite its potential relevance for the understanding of tissue regenerative processes and the design of biomaterials. Here, the role of surface curvature on the migratory and differentiation behavior of human mesenchymal stem cells (hMSCs) has been investigated on 3D surfaces with well‐defined geometric features produced by stereolithography. Time lapse microscopy reveals a significant increase of cell migration speed on concave spherical compared to convex spherical structures and flat surfaces resulting from an upward‐lift of the cell body due to cytoskeletal forces. On convex surfaces, cytoskeletal forces lead to substantial nuclear deformation, increase lamin‐A levels and promote osteogenic differentiation. The findings of this study demonstrate a so far missing link between 3D surface curvature and hMSC behavior. This will not only help to better understand the role of extracellular matrix architecture in health and disease but also give new insights in how 3D geometries can be used as a cell‐instructive material parameter in the field of biomaterial‐guided tissue regeneration. John Wiley and Sons Inc. 2016-12-20 /pmc/articles/PMC5323878/ /pubmed/28251054 http://dx.doi.org/10.1002/advs.201600347 Text en © 2016 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Werner, Maike
Blanquer, Sébastien B. G.
Haimi, Suvi P.
Korus, Gabriela
Dunlop, John W. C.
Duda, Georg N.
Grijpma, Dirk. W.
Petersen, Ansgar
Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title_full Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title_fullStr Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title_full_unstemmed Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title_short Surface Curvature Differentially Regulates Stem Cell Migration and Differentiation via Altered Attachment Morphology and Nuclear Deformation
title_sort surface curvature differentially regulates stem cell migration and differentiation via altered attachment morphology and nuclear deformation
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323878/
https://www.ncbi.nlm.nih.gov/pubmed/28251054
http://dx.doi.org/10.1002/advs.201600347
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