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...
Autores principales: | , , , , , , , , |
---|---|
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 |