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Fibroblast rejuvenation by mechanical reprogramming and redifferentiation
Over the course of the aging process, fibroblasts lose contractility, leading to reduced connective-tissue stiffness. A promising therapeutic avenue for functional rejuvenation of connective tissue is reprogrammed fibroblast replacement, although major hurdles still remain. Toward this, we recently...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229653/ https://www.ncbi.nlm.nih.gov/pubmed/32350144 http://dx.doi.org/10.1073/pnas.1911497117 |
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author | Roy, Bibhas Yuan, Luezhen Lee, Yaelim Bharti, Aradhana Mitra, Aninda Shivashankar, G. V. |
author_facet | Roy, Bibhas Yuan, Luezhen Lee, Yaelim Bharti, Aradhana Mitra, Aninda Shivashankar, G. V. |
author_sort | Roy, Bibhas |
collection | PubMed |
description | Over the course of the aging process, fibroblasts lose contractility, leading to reduced connective-tissue stiffness. A promising therapeutic avenue for functional rejuvenation of connective tissue is reprogrammed fibroblast replacement, although major hurdles still remain. Toward this, we recently demonstrated that the laterally confined growth of fibroblasts on micropatterned substrates induces stem-cell-like spheroids. In this study, we embedded these partially reprogrammed spheroids in collagen-I matrices of varying densities, mimicking different three-dimensional (3D) tissue constraints. In response to such matrix constraints, these spheroids regained their fibroblastic properties and sprouted to form 3D connective-tissue networks. Interestingly, we found that these differentiated fibroblasts exhibit reduced DNA damage, enhanced cytoskeletal gene expression, and actomyosin contractility. In addition, the rejuvenated fibroblasts show increased matrix protein (fibronectin and laminin) deposition and collagen remodeling compared to the parental fibroblast tissue network. Furthermore, we show that the partially reprogrammed cells have comparatively open chromatin compaction states and may be more poised to redifferentiate into contractile fibroblasts in 3D-collagen matrix. Collectively, our results highlight efficient fibroblast rejuvenation through laterally confined reprogramming, which has important implications in regenerative medicine. |
format | Online Article Text |
id | pubmed-7229653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-72296532020-05-26 Fibroblast rejuvenation by mechanical reprogramming and redifferentiation Roy, Bibhas Yuan, Luezhen Lee, Yaelim Bharti, Aradhana Mitra, Aninda Shivashankar, G. V. Proc Natl Acad Sci U S A Physical Sciences Over the course of the aging process, fibroblasts lose contractility, leading to reduced connective-tissue stiffness. A promising therapeutic avenue for functional rejuvenation of connective tissue is reprogrammed fibroblast replacement, although major hurdles still remain. Toward this, we recently demonstrated that the laterally confined growth of fibroblasts on micropatterned substrates induces stem-cell-like spheroids. In this study, we embedded these partially reprogrammed spheroids in collagen-I matrices of varying densities, mimicking different three-dimensional (3D) tissue constraints. In response to such matrix constraints, these spheroids regained their fibroblastic properties and sprouted to form 3D connective-tissue networks. Interestingly, we found that these differentiated fibroblasts exhibit reduced DNA damage, enhanced cytoskeletal gene expression, and actomyosin contractility. In addition, the rejuvenated fibroblasts show increased matrix protein (fibronectin and laminin) deposition and collagen remodeling compared to the parental fibroblast tissue network. Furthermore, we show that the partially reprogrammed cells have comparatively open chromatin compaction states and may be more poised to redifferentiate into contractile fibroblasts in 3D-collagen matrix. Collectively, our results highlight efficient fibroblast rejuvenation through laterally confined reprogramming, which has important implications in regenerative medicine. National Academy of Sciences 2020-05-12 2020-04-29 /pmc/articles/PMC7229653/ /pubmed/32350144 http://dx.doi.org/10.1073/pnas.1911497117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Physical Sciences Roy, Bibhas Yuan, Luezhen Lee, Yaelim Bharti, Aradhana Mitra, Aninda Shivashankar, G. V. Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title | Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title_full | Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title_fullStr | Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title_full_unstemmed | Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title_short | Fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
title_sort | fibroblast rejuvenation by mechanical reprogramming and redifferentiation |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229653/ https://www.ncbi.nlm.nih.gov/pubmed/32350144 http://dx.doi.org/10.1073/pnas.1911497117 |
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