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1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model
PURPOSE: Fat grafting is known to rejuvenate and improve fibrosis in irradiated skin, but the underlying mechanisms behind these effects are poorly understood. We have previously identified the Engrailed-1 fibroblast sub-population as having a role in post-natal dorsal skin fibrosis in mice. Using a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312817/ http://dx.doi.org/10.1097/01.GOX.0000769928.40352.e5 |
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author | Abbas, Darren B. Fahy, Evan J. Lavin, Christopher Griffin, Michelle Adem, Sandeep Diaz Deleon, Nestor M. Mascharak, Shamik King, Megan Lee, Daniel Longaker, Michael T. Wan, Derrick C. |
author_facet | Abbas, Darren B. Fahy, Evan J. Lavin, Christopher Griffin, Michelle Adem, Sandeep Diaz Deleon, Nestor M. Mascharak, Shamik King, Megan Lee, Daniel Longaker, Michael T. Wan, Derrick C. |
author_sort | Abbas, Darren B. |
collection | PubMed |
description | PURPOSE: Fat grafting is known to rejuvenate and improve fibrosis in irradiated skin, but the underlying mechanisms behind these effects are poorly understood. We have previously identified the Engrailed-1 fibroblast sub-population as having a role in post-natal dorsal skin fibrosis in mice. Using a radiation model to the scalp of Engrailed-1 mice, we sought to better understand the regenerative effects of fat grafting in irradiated tissue. METHODS: Adult (60-day old) En1(Cre);R26(mTmG) transgenic mice (n=5) underwent total body irradiation with 9 Gy for immunodepletion. Mice were then immediately reconstituted with 2 million nucleated bone marrow cells from donor NSG(NOD.CB17-Prkdcs(scid)/J) mice via retro-orbital injections. Reconstitution was confirmed with fluorescence-activated cell sorting (FACS) 2 weeks after whole body irradiation. Mice scalps were then irradiated with 5 Gy every other day for 12 days (30 Gy total) and allowed to recover for 4 weeks to facilitate fibrotic conversion. Irradiated scalps were grafted with 200μL of fresh human lipoaspirate. Graph retention was measured in-vivo for 8 weeks using Micro-Computed Tomography Scanner (Bruker SkyScan 1726(™)) and scalp skin was harvest for histology. RESULTS: Two weeks post bone-marrow transplant, >90% of circulating hematopoietic cells (CD45(+)) cells in En1(Cre);R26(mTmG) reporter mice were non-fluorescent, signifying successful reconstitution. Volumetric analysis of fat grafting in-vivo was performed using 3-dimensional reconstruction. At 8 weeks post-grafting, 4 of the 5 grafts demonstrated >50% graft retention, confirming successful grafting. Histological sections of scalp skin 8 weeks post-grafting demonstrated significantly less En1+GFP cells compared to non-grafted scalp skin, signifying less presence of En1(+) fibroblasts. Furthermore, histology demonstrated significantly less dermal thickening, epidermal thinning, and collagen deposition and disorganization in fat grafted irradiated scalp skin compared to non-grafted scalp skin. CONCLUSION: Fat grafting mitigates radiation-induced fibrosis in scalp skin by decreasing collagen deposition, remodeling collagen formation, decreasing epidermal thinning, and reducing presence of pro-fibrotic fibroblast sub-populations. |
format | Online Article Text |
id | pubmed-8312817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-83128172021-07-27 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model Abbas, Darren B. Fahy, Evan J. Lavin, Christopher Griffin, Michelle Adem, Sandeep Diaz Deleon, Nestor M. Mascharak, Shamik King, Megan Lee, Daniel Longaker, Michael T. Wan, Derrick C. Plast Reconstr Surg Glob Open PSRC 2021 Abstract Supplement PURPOSE: Fat grafting is known to rejuvenate and improve fibrosis in irradiated skin, but the underlying mechanisms behind these effects are poorly understood. We have previously identified the Engrailed-1 fibroblast sub-population as having a role in post-natal dorsal skin fibrosis in mice. Using a radiation model to the scalp of Engrailed-1 mice, we sought to better understand the regenerative effects of fat grafting in irradiated tissue. METHODS: Adult (60-day old) En1(Cre);R26(mTmG) transgenic mice (n=5) underwent total body irradiation with 9 Gy for immunodepletion. Mice were then immediately reconstituted with 2 million nucleated bone marrow cells from donor NSG(NOD.CB17-Prkdcs(scid)/J) mice via retro-orbital injections. Reconstitution was confirmed with fluorescence-activated cell sorting (FACS) 2 weeks after whole body irradiation. Mice scalps were then irradiated with 5 Gy every other day for 12 days (30 Gy total) and allowed to recover for 4 weeks to facilitate fibrotic conversion. Irradiated scalps were grafted with 200μL of fresh human lipoaspirate. Graph retention was measured in-vivo for 8 weeks using Micro-Computed Tomography Scanner (Bruker SkyScan 1726(™)) and scalp skin was harvest for histology. RESULTS: Two weeks post bone-marrow transplant, >90% of circulating hematopoietic cells (CD45(+)) cells in En1(Cre);R26(mTmG) reporter mice were non-fluorescent, signifying successful reconstitution. Volumetric analysis of fat grafting in-vivo was performed using 3-dimensional reconstruction. At 8 weeks post-grafting, 4 of the 5 grafts demonstrated >50% graft retention, confirming successful grafting. Histological sections of scalp skin 8 weeks post-grafting demonstrated significantly less En1+GFP cells compared to non-grafted scalp skin, signifying less presence of En1(+) fibroblasts. Furthermore, histology demonstrated significantly less dermal thickening, epidermal thinning, and collagen deposition and disorganization in fat grafted irradiated scalp skin compared to non-grafted scalp skin. CONCLUSION: Fat grafting mitigates radiation-induced fibrosis in scalp skin by decreasing collagen deposition, remodeling collagen formation, decreasing epidermal thinning, and reducing presence of pro-fibrotic fibroblast sub-populations. Lippincott Williams & Wilkins 2021-07-26 /pmc/articles/PMC8312817/ http://dx.doi.org/10.1097/01.GOX.0000769928.40352.e5 Text en Copyright © 2021 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | PSRC 2021 Abstract Supplement Abbas, Darren B. Fahy, Evan J. Lavin, Christopher Griffin, Michelle Adem, Sandeep Diaz Deleon, Nestor M. Mascharak, Shamik King, Megan Lee, Daniel Longaker, Michael T. Wan, Derrick C. 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title | 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title_full | 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title_fullStr | 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title_full_unstemmed | 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title_short | 1: Fat Grafting Improves Dorsal Skin Fibrosis after Radiation in an Engrailed-1 Mouse Model |
title_sort | 1: fat grafting improves dorsal skin fibrosis after radiation in an engrailed-1 mouse model |
topic | PSRC 2021 Abstract Supplement |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312817/ http://dx.doi.org/10.1097/01.GOX.0000769928.40352.e5 |
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