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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
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.
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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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