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Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation

Specific protein-cell and drug-cell interactions have been widely used to manipulate stem cell fate. Despite extensive studies, most current platforms cannot realize reversible manipulation of stem cell differentiation. In this work, we report a photodynamic zwitterionic hydrogel capable of reversib...

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Autores principales: Bai, Tao, Sinclair, Andrew, Sun, Fang, Jain, Priyesh, Hung, Hsiang-Chieh, Zhang, Peng, Ella-Menye, Jean-Rene, Liu, Wenguang, Jiang, Shaoyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518545/
https://www.ncbi.nlm.nih.gov/pubmed/28791097
http://dx.doi.org/10.1039/c5sc03244j
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author Bai, Tao
Sinclair, Andrew
Sun, Fang
Jain, Priyesh
Hung, Hsiang-Chieh
Zhang, Peng
Ella-Menye, Jean-Rene
Liu, Wenguang
Jiang, Shaoyi
author_facet Bai, Tao
Sinclair, Andrew
Sun, Fang
Jain, Priyesh
Hung, Hsiang-Chieh
Zhang, Peng
Ella-Menye, Jean-Rene
Liu, Wenguang
Jiang, Shaoyi
author_sort Bai, Tao
collection PubMed
description Specific protein-cell and drug-cell interactions have been widely used to manipulate stem cell fate. Despite extensive studies, most current platforms cannot realize reversible manipulation of stem cell differentiation. In this work, we report a photodynamic zwitterionic hydrogel capable of reversibly triggering and suspending the differentiation process via manipulating nonspecific interactions between cultured stem cells and the hydrogel. The differentiation state of stem cells can be altered by exposing the hydrogel to a selected light program, while differentiation can be immediately suspended when near-infrared exposure converts the hydrogel into a purely zwitterionic form. While many other studies apply specific interactions to control stem cell fate, this work provides a completely different approach—allowing reversible, real-time and localized manipulation of stem cell fate choice via nonspecific interactions.
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spelling pubmed-55185452017-08-08 Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation Bai, Tao Sinclair, Andrew Sun, Fang Jain, Priyesh Hung, Hsiang-Chieh Zhang, Peng Ella-Menye, Jean-Rene Liu, Wenguang Jiang, Shaoyi Chem Sci Chemistry Specific protein-cell and drug-cell interactions have been widely used to manipulate stem cell fate. Despite extensive studies, most current platforms cannot realize reversible manipulation of stem cell differentiation. In this work, we report a photodynamic zwitterionic hydrogel capable of reversibly triggering and suspending the differentiation process via manipulating nonspecific interactions between cultured stem cells and the hydrogel. The differentiation state of stem cells can be altered by exposing the hydrogel to a selected light program, while differentiation can be immediately suspended when near-infrared exposure converts the hydrogel into a purely zwitterionic form. While many other studies apply specific interactions to control stem cell fate, this work provides a completely different approach—allowing reversible, real-time and localized manipulation of stem cell fate choice via nonspecific interactions. Royal Society of Chemistry 2016-01-01 2015-10-07 /pmc/articles/PMC5518545/ /pubmed/28791097 http://dx.doi.org/10.1039/c5sc03244j Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Bai, Tao
Sinclair, Andrew
Sun, Fang
Jain, Priyesh
Hung, Hsiang-Chieh
Zhang, Peng
Ella-Menye, Jean-Rene
Liu, Wenguang
Jiang, Shaoyi
Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title_full Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title_fullStr Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title_full_unstemmed Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title_short Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
title_sort harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518545/
https://www.ncbi.nlm.nih.gov/pubmed/28791097
http://dx.doi.org/10.1039/c5sc03244j
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