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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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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. |
format | Online Article Text |
id | pubmed-5518545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
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title_fullStr | Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
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title_full_unstemmed | Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
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title_short | Harnessing isomerization-mediated manipulation of nonspecific cell/matrix interactions to reversibly trigger and suspend stem cell differentiation
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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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