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Dynamically Modulated Core–Shell Microfibers to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell Fate
[Image: see text] It is well known that extracellular matrix stiffness can affect cell fate and change dynamically during many biological processes. Existing experimental means for in situ matrix stiffness modulation often alters its structure, which could induce additional undesirable effects on ce...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397254/ https://www.ncbi.nlm.nih.gov/pubmed/34355561 http://dx.doi.org/10.1021/acsami.1c06752 |
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author | Wei, Dan Charlton, Laura Glidle, Andrew Qi, Nan Dobson, Phillip S. Dalby, Matthew John Fan, Hongsong Yin, Huabing |
author_facet | Wei, Dan Charlton, Laura Glidle, Andrew Qi, Nan Dobson, Phillip S. Dalby, Matthew John Fan, Hongsong Yin, Huabing |
author_sort | Wei, Dan |
collection | PubMed |
description | [Image: see text] It is well known that extracellular matrix stiffness can affect cell fate and change dynamically during many biological processes. Existing experimental means for in situ matrix stiffness modulation often alters its structure, which could induce additional undesirable effects on cells. Inspired by the phenomenon of depth sensing by cells, we introduce here core–shell microfibers with a thin collagen core for cell growth and an alginate shell that can be dynamically stiffened to deliver mechanical stimuli. This allows for the maintenance of biochemical properties and structure of the surrounding microenvironment, while dynamically modulating the effective modulus “felt” by cells. We show that simple addition of Sr(2+) in media can easily increase the stiffness of initially Ca(2+) cross-linked alginate shells. Thus, despite the low stiffness of collagen cores (<5 kPa), the effective modulus of the matrix “felt” by cells are substantially higher, which promotes osteogenesis differentiation of human mesenchymal stem cells. We show this effect is more prominent in the stiffening microfiber compared to a static microfiber control. This approach provides a versatile platform to independently and dynamically modulate cellular microenvironments with desirable biochemical, physical, and mechanical stimuli without an unintended interplay of effects, facilitating investigations of a wide range of dynamic cellular processes. |
format | Online Article Text |
id | pubmed-8397254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83972542021-08-31 Dynamically Modulated Core–Shell Microfibers to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell Fate Wei, Dan Charlton, Laura Glidle, Andrew Qi, Nan Dobson, Phillip S. Dalby, Matthew John Fan, Hongsong Yin, Huabing ACS Appl Mater Interfaces [Image: see text] It is well known that extracellular matrix stiffness can affect cell fate and change dynamically during many biological processes. Existing experimental means for in situ matrix stiffness modulation often alters its structure, which could induce additional undesirable effects on cells. Inspired by the phenomenon of depth sensing by cells, we introduce here core–shell microfibers with a thin collagen core for cell growth and an alginate shell that can be dynamically stiffened to deliver mechanical stimuli. This allows for the maintenance of biochemical properties and structure of the surrounding microenvironment, while dynamically modulating the effective modulus “felt” by cells. We show that simple addition of Sr(2+) in media can easily increase the stiffness of initially Ca(2+) cross-linked alginate shells. Thus, despite the low stiffness of collagen cores (<5 kPa), the effective modulus of the matrix “felt” by cells are substantially higher, which promotes osteogenesis differentiation of human mesenchymal stem cells. We show this effect is more prominent in the stiffening microfiber compared to a static microfiber control. This approach provides a versatile platform to independently and dynamically modulate cellular microenvironments with desirable biochemical, physical, and mechanical stimuli without an unintended interplay of effects, facilitating investigations of a wide range of dynamic cellular processes. American Chemical Society 2021-08-06 2021-08-18 /pmc/articles/PMC8397254/ /pubmed/34355561 http://dx.doi.org/10.1021/acsami.1c06752 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Wei, Dan Charlton, Laura Glidle, Andrew Qi, Nan Dobson, Phillip S. Dalby, Matthew John Fan, Hongsong Yin, Huabing Dynamically Modulated Core–Shell Microfibers to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell Fate |
title | Dynamically Modulated Core–Shell Microfibers
to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell
Fate |
title_full | Dynamically Modulated Core–Shell Microfibers
to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell
Fate |
title_fullStr | Dynamically Modulated Core–Shell Microfibers
to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell
Fate |
title_full_unstemmed | Dynamically Modulated Core–Shell Microfibers
to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell
Fate |
title_short | Dynamically Modulated Core–Shell Microfibers
to Study the Effect of Depth Sensing of Matrix Stiffness on Stem Cell
Fate |
title_sort | dynamically modulated core–shell microfibers
to study the effect of depth sensing of matrix stiffness on stem cell
fate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397254/ https://www.ncbi.nlm.nih.gov/pubmed/34355561 http://dx.doi.org/10.1021/acsami.1c06752 |
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