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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...

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Autores principales: Roy, Bibhas, Yuan, Luezhen, Lee, Yaelim, Bharti, Aradhana, Mitra, Aninda, Shivashankar, G. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
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.
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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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