Cargando…

Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis

The topography of a biomaterial regulates cellular interactions and determine stem cell fate. A complete understanding of how topographical properties affect cell behavior will allow the rational design of material surfaces that elicit specified biological functions once placed in the body. To this...

Descripción completa

Detalles Bibliográficos
Autores principales: Newman, Peter, Galenano-Niño, Jorge Luis, Graney, Pamela, Razal, Joselito M., Minett, Andrew I., Ribas, João, Ovalle-Robles, Raquel, Biro, Maté, Zreiqat, Hala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133629/
https://www.ncbi.nlm.nih.gov/pubmed/27910868
http://dx.doi.org/10.1038/srep37909
_version_ 1782471304292597760
author Newman, Peter
Galenano-Niño, Jorge Luis
Graney, Pamela
Razal, Joselito M.
Minett, Andrew I.
Ribas, João
Ovalle-Robles, Raquel
Biro, Maté
Zreiqat, Hala
author_facet Newman, Peter
Galenano-Niño, Jorge Luis
Graney, Pamela
Razal, Joselito M.
Minett, Andrew I.
Ribas, João
Ovalle-Robles, Raquel
Biro, Maté
Zreiqat, Hala
author_sort Newman, Peter
collection PubMed
description The topography of a biomaterial regulates cellular interactions and determine stem cell fate. A complete understanding of how topographical properties affect cell behavior will allow the rational design of material surfaces that elicit specified biological functions once placed in the body. To this end, we fabricate substrates with aligned or randomly organized fibrous nanostructured topographies. Culturing adipose-derived stem cells (ASCs), we explore the dynamic relationship between the alignment of topography, cell shape and cell differentiation to osteogenic and myogenic lineages. We show aligned topographies differentiate cells towards a satellite cell muscle progenitor state - a distinct cell myogenic lineage responsible for postnatal growth and repair of muscle. We analyze cell shape between the different topographies, using fluorescent time-lapse imaging over 21 days. In contrast to previous work, this allows the direct measurement of cell shape at a given time rather than defining the morphology of the underlying topography and neglecting cell shape. We report quantitative metrics of the time-based morphological behaviors of cell shape in response to differing topographies. This analysis offers insights into the relationship between topography, cell shape and cell differentiation. Cells differentiating towards a myogenic fate on aligned topographies adopt a characteristic elongated shape as well as the alignment of cells.
format Online
Article
Text
id pubmed-5133629
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-51336292017-01-27 Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis Newman, Peter Galenano-Niño, Jorge Luis Graney, Pamela Razal, Joselito M. Minett, Andrew I. Ribas, João Ovalle-Robles, Raquel Biro, Maté Zreiqat, Hala Sci Rep Article The topography of a biomaterial regulates cellular interactions and determine stem cell fate. A complete understanding of how topographical properties affect cell behavior will allow the rational design of material surfaces that elicit specified biological functions once placed in the body. To this end, we fabricate substrates with aligned or randomly organized fibrous nanostructured topographies. Culturing adipose-derived stem cells (ASCs), we explore the dynamic relationship between the alignment of topography, cell shape and cell differentiation to osteogenic and myogenic lineages. We show aligned topographies differentiate cells towards a satellite cell muscle progenitor state - a distinct cell myogenic lineage responsible for postnatal growth and repair of muscle. We analyze cell shape between the different topographies, using fluorescent time-lapse imaging over 21 days. In contrast to previous work, this allows the direct measurement of cell shape at a given time rather than defining the morphology of the underlying topography and neglecting cell shape. We report quantitative metrics of the time-based morphological behaviors of cell shape in response to differing topographies. This analysis offers insights into the relationship between topography, cell shape and cell differentiation. Cells differentiating towards a myogenic fate on aligned topographies adopt a characteristic elongated shape as well as the alignment of cells. Nature Publishing Group 2016-12-02 /pmc/articles/PMC5133629/ /pubmed/27910868 http://dx.doi.org/10.1038/srep37909 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Newman, Peter
Galenano-Niño, Jorge Luis
Graney, Pamela
Razal, Joselito M.
Minett, Andrew I.
Ribas, João
Ovalle-Robles, Raquel
Biro, Maté
Zreiqat, Hala
Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title_full Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title_fullStr Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title_full_unstemmed Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title_short Relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
title_sort relationship between nanotopographical alignment and stem cell fate with live imaging and shape analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133629/
https://www.ncbi.nlm.nih.gov/pubmed/27910868
http://dx.doi.org/10.1038/srep37909
work_keys_str_mv AT newmanpeter relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT galenanoninojorgeluis relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT graneypamela relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT razaljoselitom relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT minettandrewi relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT ribasjoao relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT ovalleroblesraquel relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT biromate relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis
AT zreiqathala relationshipbetweennanotopographicalalignmentandstemcellfatewithliveimagingandshapeanalysis