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Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model
Microgravity impairs tissue organization and critical pathways involved in the cell–microenvironment interplay, where fibroblasts have a critical role. We exposed dermal fibroblasts to simulated microgravity by means of a Random Positioning Machine (RPM), a device that reproduces conditions of weigh...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879576/ https://www.ncbi.nlm.nih.gov/pubmed/35216279 http://dx.doi.org/10.3390/ijms23042163 |
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author | Fedeli, Valeria Cucina, Alessandra Dinicola, Simona Fabrizi, Gianmarco Catizone, Angela Gesualdi, Luisa Ceccarelli, Simona Harrath, Abdel Halim Alwasel, Saleh H. Ricci, Giulia Pedata, Paola Bizzarri, Mariano Monti, Noemi |
author_facet | Fedeli, Valeria Cucina, Alessandra Dinicola, Simona Fabrizi, Gianmarco Catizone, Angela Gesualdi, Luisa Ceccarelli, Simona Harrath, Abdel Halim Alwasel, Saleh H. Ricci, Giulia Pedata, Paola Bizzarri, Mariano Monti, Noemi |
author_sort | Fedeli, Valeria |
collection | PubMed |
description | Microgravity impairs tissue organization and critical pathways involved in the cell–microenvironment interplay, where fibroblasts have a critical role. We exposed dermal fibroblasts to simulated microgravity by means of a Random Positioning Machine (RPM), a device that reproduces conditions of weightlessness. Molecular and structural changes were analyzed and compared to control samples growing in a normal gravity field. Simulated microgravity impairs fibroblast conversion into myofibroblast and inhibits their migratory properties. Consequently, the normal interplay between fibroblasts and keratinocytes were remarkably altered in 3D co-culture experiments, giving rise to several ultra-structural abnormalities. Such phenotypic changes are associated with down-regulation of α-SMA that translocate in the nucleoplasm, altogether with the concomitant modification of the actin-vinculin apparatus. Noticeably, the stress associated with weightlessness induced oxidative damage, which seemed to concur with such modifications. These findings disclose new opportunities to establish antioxidant strategies that counteract the microgravity-induced disruptive effects on fibroblasts and tissue organization. |
format | Online Article Text |
id | pubmed-8879576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88795762022-02-26 Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model Fedeli, Valeria Cucina, Alessandra Dinicola, Simona Fabrizi, Gianmarco Catizone, Angela Gesualdi, Luisa Ceccarelli, Simona Harrath, Abdel Halim Alwasel, Saleh H. Ricci, Giulia Pedata, Paola Bizzarri, Mariano Monti, Noemi Int J Mol Sci Article Microgravity impairs tissue organization and critical pathways involved in the cell–microenvironment interplay, where fibroblasts have a critical role. We exposed dermal fibroblasts to simulated microgravity by means of a Random Positioning Machine (RPM), a device that reproduces conditions of weightlessness. Molecular and structural changes were analyzed and compared to control samples growing in a normal gravity field. Simulated microgravity impairs fibroblast conversion into myofibroblast and inhibits their migratory properties. Consequently, the normal interplay between fibroblasts and keratinocytes were remarkably altered in 3D co-culture experiments, giving rise to several ultra-structural abnormalities. Such phenotypic changes are associated with down-regulation of α-SMA that translocate in the nucleoplasm, altogether with the concomitant modification of the actin-vinculin apparatus. Noticeably, the stress associated with weightlessness induced oxidative damage, which seemed to concur with such modifications. These findings disclose new opportunities to establish antioxidant strategies that counteract the microgravity-induced disruptive effects on fibroblasts and tissue organization. MDPI 2022-02-16 /pmc/articles/PMC8879576/ /pubmed/35216279 http://dx.doi.org/10.3390/ijms23042163 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fedeli, Valeria Cucina, Alessandra Dinicola, Simona Fabrizi, Gianmarco Catizone, Angela Gesualdi, Luisa Ceccarelli, Simona Harrath, Abdel Halim Alwasel, Saleh H. Ricci, Giulia Pedata, Paola Bizzarri, Mariano Monti, Noemi Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title | Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title_full | Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title_fullStr | Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title_full_unstemmed | Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title_short | Microgravity Modifies the Phenotype of Fibroblast and Promotes Remodeling of the Fibroblast–Keratinocyte Interaction in a 3D Co-Culture Model |
title_sort | microgravity modifies the phenotype of fibroblast and promotes remodeling of the fibroblast–keratinocyte interaction in a 3d co-culture model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879576/ https://www.ncbi.nlm.nih.gov/pubmed/35216279 http://dx.doi.org/10.3390/ijms23042163 |
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