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Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation

Cellular biophysical properties are novel biomarkers of cell phenotypes which may reflect the status of differentiating stem cells. Accurate characterizations of cellular biophysical properties, in conjunction with the corresponding biochemical properties could help to distinguish stem cells from pr...

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Autores principales: Chen, Yin-Quan, Liu, Yi-Shiuan, Liu, Yu-An, Wu, Yi-Chang, del Álamo, Juan C., Chiou, Arthur, Lee, Oscar K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985743/
https://www.ncbi.nlm.nih.gov/pubmed/27526936
http://dx.doi.org/10.1038/srep31547
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author Chen, Yin-Quan
Liu, Yi-Shiuan
Liu, Yu-An
Wu, Yi-Chang
del Álamo, Juan C.
Chiou, Arthur
Lee, Oscar K.
author_facet Chen, Yin-Quan
Liu, Yi-Shiuan
Liu, Yu-An
Wu, Yi-Chang
del Álamo, Juan C.
Chiou, Arthur
Lee, Oscar K.
author_sort Chen, Yin-Quan
collection PubMed
description Cellular biophysical properties are novel biomarkers of cell phenotypes which may reflect the status of differentiating stem cells. Accurate characterizations of cellular biophysical properties, in conjunction with the corresponding biochemical properties could help to distinguish stem cells from primary cells, cancer cells, and differentiated cells. However, the correlated evolution of these properties in the course of directed stem cells differentiation has not been well characterized. In this study, we applied video particle tracking microrheology (VPTM) to measure intracellular viscoelasticity of differentiating human mesenchymal stromal/stem cells (hMSCs). Our results showed that osteogenesis not only increased both elastic and viscous moduli, but also converted the intracellular viscoelasticity of differentiating hMSCs from viscous-like to elastic-like. In contrast, adipogenesis decreased both elastic and viscous moduli while hMSCs remained viscous-like during the differentiation. In conjunction with bio- chemical and physical parameters, such as gene expression profiles, cell morphology, and cytoskeleton arrangement, we demonstrated that VPTM is a unique approach to quantify, with high data throughput, the maturation level of differentiating hMSCs and to anticipate their fate decisions. This approach is well suited for time-lapsed study of the mechanobiology of differentiating stem cells especially in three dimensional physico-chemical biomimetic environments including porous scaffolds.
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spelling pubmed-49857432016-08-22 Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation Chen, Yin-Quan Liu, Yi-Shiuan Liu, Yu-An Wu, Yi-Chang del Álamo, Juan C. Chiou, Arthur Lee, Oscar K. Sci Rep Article Cellular biophysical properties are novel biomarkers of cell phenotypes which may reflect the status of differentiating stem cells. Accurate characterizations of cellular biophysical properties, in conjunction with the corresponding biochemical properties could help to distinguish stem cells from primary cells, cancer cells, and differentiated cells. However, the correlated evolution of these properties in the course of directed stem cells differentiation has not been well characterized. In this study, we applied video particle tracking microrheology (VPTM) to measure intracellular viscoelasticity of differentiating human mesenchymal stromal/stem cells (hMSCs). Our results showed that osteogenesis not only increased both elastic and viscous moduli, but also converted the intracellular viscoelasticity of differentiating hMSCs from viscous-like to elastic-like. In contrast, adipogenesis decreased both elastic and viscous moduli while hMSCs remained viscous-like during the differentiation. In conjunction with bio- chemical and physical parameters, such as gene expression profiles, cell morphology, and cytoskeleton arrangement, we demonstrated that VPTM is a unique approach to quantify, with high data throughput, the maturation level of differentiating hMSCs and to anticipate their fate decisions. This approach is well suited for time-lapsed study of the mechanobiology of differentiating stem cells especially in three dimensional physico-chemical biomimetic environments including porous scaffolds. Nature Publishing Group 2016-08-16 /pmc/articles/PMC4985743/ /pubmed/27526936 http://dx.doi.org/10.1038/srep31547 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
Chen, Yin-Quan
Liu, Yi-Shiuan
Liu, Yu-An
Wu, Yi-Chang
del Álamo, Juan C.
Chiou, Arthur
Lee, Oscar K.
Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title_full Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title_fullStr Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title_full_unstemmed Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title_short Bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
title_sort bio- chemical and physical characterizations of mesenchymal stromal cells along the time course of directed differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985743/
https://www.ncbi.nlm.nih.gov/pubmed/27526936
http://dx.doi.org/10.1038/srep31547
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