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Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps

Reconstructive transplantation such as extremity and face transplantation is a viable treatment option for select patients with devastating tissue loss. Sensorimotor recovery is a critical determinant of overall success of such transplants. Although motor function recovery has been extensively studi...

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Autores principales: Ibrahim, Zuhaib, Ebenezer, Gigi, Christensen, Joani M., Sarhane, Karim A., Hauer, Peter, Cooney, Damon S., Sacks, Justin M., Schneeberger, Stefan, Lee, W. P. Andrew, Polydefkis, Michael, Brandacher, Gerald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799840/
https://www.ncbi.nlm.nih.gov/pubmed/24204901
http://dx.doi.org/10.1371/journal.pone.0077646
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author Ibrahim, Zuhaib
Ebenezer, Gigi
Christensen, Joani M.
Sarhane, Karim A.
Hauer, Peter
Cooney, Damon S.
Sacks, Justin M.
Schneeberger, Stefan
Lee, W. P. Andrew
Polydefkis, Michael
Brandacher, Gerald
author_facet Ibrahim, Zuhaib
Ebenezer, Gigi
Christensen, Joani M.
Sarhane, Karim A.
Hauer, Peter
Cooney, Damon S.
Sacks, Justin M.
Schneeberger, Stefan
Lee, W. P. Andrew
Polydefkis, Michael
Brandacher, Gerald
author_sort Ibrahim, Zuhaib
collection PubMed
description Reconstructive transplantation such as extremity and face transplantation is a viable treatment option for select patients with devastating tissue loss. Sensorimotor recovery is a critical determinant of overall success of such transplants. Although motor function recovery has been extensively studied, mechanisms of sensory re-innervation are not well established. Recent clinical reports of face transplants confirm progressive sensory improvement even in cases where optimal repair of sensory nerves was not achieved. Two forms of sensory nerve regeneration are known. In regenerative sprouting, axonal outgrowth occurs from the transected nerve stump while in collateral sprouting, reinnervation of denervated tissue occurs through growth of uninjured axons into the denervated tissue. The latter mechanism may be more important in settings where transected sensory nerves cannot be re-apposed. In this study, denervated osteomyocutaneous alloflaps (hind- limb transplants) from Major Histocompatibility Complex (MHC)-defined MGH miniature swine were performed to specifically evaluate collateral axonal sprouting for cutaneous sensory re-innervation. The skin component of the flap was externalized and serial skin sections extending from native skin to the grafted flap were biopsied. In order to visualize regenerating axonal structures in the dermis and epidermis, 50um frozen sections were immunostained against axonal and Schwann cell markers. In all alloflaps, collateral axonal sprouts from adjacent recipient skin extended into the denervated skin component along the dermal-epidermal junction from the periphery towards the center. On day 100 post-transplant, regenerating sprouts reached 0.5 cm into the flap centripetally. Eight months following transplant, epidermal fibers were visualized 1.5 cm from the margin (rate of regeneration 0.06 mm per day). All animals had pinprick sensation in the periphery of the transplanted skin within 3 months post-transplant. Restoration of sensory input through collateral axonal sprouting can revive interaction with the environment; restore defense mechanisms and aid in cortical re-integration of vascularized composite allografts.
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spelling pubmed-37998402013-11-07 Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps Ibrahim, Zuhaib Ebenezer, Gigi Christensen, Joani M. Sarhane, Karim A. Hauer, Peter Cooney, Damon S. Sacks, Justin M. Schneeberger, Stefan Lee, W. P. Andrew Polydefkis, Michael Brandacher, Gerald PLoS One Research Article Reconstructive transplantation such as extremity and face transplantation is a viable treatment option for select patients with devastating tissue loss. Sensorimotor recovery is a critical determinant of overall success of such transplants. Although motor function recovery has been extensively studied, mechanisms of sensory re-innervation are not well established. Recent clinical reports of face transplants confirm progressive sensory improvement even in cases where optimal repair of sensory nerves was not achieved. Two forms of sensory nerve regeneration are known. In regenerative sprouting, axonal outgrowth occurs from the transected nerve stump while in collateral sprouting, reinnervation of denervated tissue occurs through growth of uninjured axons into the denervated tissue. The latter mechanism may be more important in settings where transected sensory nerves cannot be re-apposed. In this study, denervated osteomyocutaneous alloflaps (hind- limb transplants) from Major Histocompatibility Complex (MHC)-defined MGH miniature swine were performed to specifically evaluate collateral axonal sprouting for cutaneous sensory re-innervation. The skin component of the flap was externalized and serial skin sections extending from native skin to the grafted flap were biopsied. In order to visualize regenerating axonal structures in the dermis and epidermis, 50um frozen sections were immunostained against axonal and Schwann cell markers. In all alloflaps, collateral axonal sprouts from adjacent recipient skin extended into the denervated skin component along the dermal-epidermal junction from the periphery towards the center. On day 100 post-transplant, regenerating sprouts reached 0.5 cm into the flap centripetally. Eight months following transplant, epidermal fibers were visualized 1.5 cm from the margin (rate of regeneration 0.06 mm per day). All animals had pinprick sensation in the periphery of the transplanted skin within 3 months post-transplant. Restoration of sensory input through collateral axonal sprouting can revive interaction with the environment; restore defense mechanisms and aid in cortical re-integration of vascularized composite allografts. Public Library of Science 2013-10-18 /pmc/articles/PMC3799840/ /pubmed/24204901 http://dx.doi.org/10.1371/journal.pone.0077646 Text en © 2013 Ibrahim et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ibrahim, Zuhaib
Ebenezer, Gigi
Christensen, Joani M.
Sarhane, Karim A.
Hauer, Peter
Cooney, Damon S.
Sacks, Justin M.
Schneeberger, Stefan
Lee, W. P. Andrew
Polydefkis, Michael
Brandacher, Gerald
Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title_full Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title_fullStr Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title_full_unstemmed Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title_short Cutaneous Collateral Axonal Sprouting Re-Innervates the Skin Component and Restores Sensation of Denervated Swine Osteomyocutaneous Alloflaps
title_sort cutaneous collateral axonal sprouting re-innervates the skin component and restores sensation of denervated swine osteomyocutaneous alloflaps
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799840/
https://www.ncbi.nlm.nih.gov/pubmed/24204901
http://dx.doi.org/10.1371/journal.pone.0077646
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