Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures.
The highly proliferative and pluripotent characteristics of embryonic stem cells engender great promise for tissue engineering and regenerative medicine, but the rapid identification and isolation of target cell phenotypes remains challenging. Therefore, the objectives of this study were to characte...
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doaj-034f79755c7847a6b504cfe8c3fc23792020-11-25T01:45:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019263110.1371/journal.pone.0192631Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures.Tom BongiornoJeremy GuraPriyanka TalwarDwight ChambersKatherine M YoungDalia ArafatGonghao WangEmily L Jackson-HolmesPeng QiuTodd C McDevittTodd SulchekThe highly proliferative and pluripotent characteristics of embryonic stem cells engender great promise for tissue engineering and regenerative medicine, but the rapid identification and isolation of target cell phenotypes remains challenging. Therefore, the objectives of this study were to characterize cell mechanics as a function of differentiation and to employ differences in cell stiffness to select population subsets with distinct mechanical, morphological, and biological properties. Biomechanical analysis with atomic force microscopy revealed that embryonic stem cells stiffened within one day of differentiation induced by leukemia inhibitory factor removal, with a lagging but pronounced change from spherical to spindle-shaped cell morphology. A microfluidic device was then employed to sort a differentially labeled mixture of pluripotent and differentiating cells based on stiffness, resulting in pluripotent cell enrichment in the soft device outlet. Furthermore, sorting an unlabeled population of partially differentiated cells produced a subset of "soft" cells that was enriched for the pluripotent phenotype, as assessed by post-sort characterization of cell mechanics, morphology, and gene expression. The results of this study indicate that intrinsic cell mechanical properties might serve as a basis for efficient, high-throughput, and label-free isolation of pluripotent stem cells, which will facilitate a greater biological understanding of pluripotency and advance the potential of pluripotent stem cell differentiated progeny as cell sources for tissue engineering and regenerative medicine.http://europepmc.org/articles/PMC5843178?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tom Bongiorno Jeremy Gura Priyanka Talwar Dwight Chambers Katherine M Young Dalia Arafat Gonghao Wang Emily L Jackson-Holmes Peng Qiu Todd C McDevitt Todd Sulchek |
spellingShingle |
Tom Bongiorno Jeremy Gura Priyanka Talwar Dwight Chambers Katherine M Young Dalia Arafat Gonghao Wang Emily L Jackson-Holmes Peng Qiu Todd C McDevitt Todd Sulchek Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. PLoS ONE |
author_facet |
Tom Bongiorno Jeremy Gura Priyanka Talwar Dwight Chambers Katherine M Young Dalia Arafat Gonghao Wang Emily L Jackson-Holmes Peng Qiu Todd C McDevitt Todd Sulchek |
author_sort |
Tom Bongiorno |
title |
Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
title_short |
Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
title_full |
Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
title_fullStr |
Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
title_full_unstemmed |
Biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
title_sort |
biophysical subsets of embryonic stem cells display distinct phenotypic and morphological signatures. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2018-01-01 |
description |
The highly proliferative and pluripotent characteristics of embryonic stem cells engender great promise for tissue engineering and regenerative medicine, but the rapid identification and isolation of target cell phenotypes remains challenging. Therefore, the objectives of this study were to characterize cell mechanics as a function of differentiation and to employ differences in cell stiffness to select population subsets with distinct mechanical, morphological, and biological properties. Biomechanical analysis with atomic force microscopy revealed that embryonic stem cells stiffened within one day of differentiation induced by leukemia inhibitory factor removal, with a lagging but pronounced change from spherical to spindle-shaped cell morphology. A microfluidic device was then employed to sort a differentially labeled mixture of pluripotent and differentiating cells based on stiffness, resulting in pluripotent cell enrichment in the soft device outlet. Furthermore, sorting an unlabeled population of partially differentiated cells produced a subset of "soft" cells that was enriched for the pluripotent phenotype, as assessed by post-sort characterization of cell mechanics, morphology, and gene expression. The results of this study indicate that intrinsic cell mechanical properties might serve as a basis for efficient, high-throughput, and label-free isolation of pluripotent stem cells, which will facilitate a greater biological understanding of pluripotency and advance the potential of pluripotent stem cell differentiated progeny as cell sources for tissue engineering and regenerative medicine. |
url |
http://europepmc.org/articles/PMC5843178?pdf=render |
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