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Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering

The loss of skin integrity has always represented a major challenge for clinicians dealing with dermal defects, such as ulcers (diabetic, vascular and chronic), postoncologic resections (i.e., radical vulvectomy) or dermatologic disorders. The introduction in recent decades of acellular dermal matri...

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Autores principales: Agostinis, Chiara, Spazzapan, Mariagiulia, Vuerich, Roman, Balduit, Andrea, Stocco, Chiara, Mangogna, Alessandro, Ricci, Giuseppe, Papa, Giovanni, Zacchigna, Serena, Bulla, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533449/
https://www.ncbi.nlm.nih.gov/pubmed/34680575
http://dx.doi.org/10.3390/biomedicines9101458
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author Agostinis, Chiara
Spazzapan, Mariagiulia
Vuerich, Roman
Balduit, Andrea
Stocco, Chiara
Mangogna, Alessandro
Ricci, Giuseppe
Papa, Giovanni
Zacchigna, Serena
Bulla, Roberta
author_facet Agostinis, Chiara
Spazzapan, Mariagiulia
Vuerich, Roman
Balduit, Andrea
Stocco, Chiara
Mangogna, Alessandro
Ricci, Giuseppe
Papa, Giovanni
Zacchigna, Serena
Bulla, Roberta
author_sort Agostinis, Chiara
collection PubMed
description The loss of skin integrity has always represented a major challenge for clinicians dealing with dermal defects, such as ulcers (diabetic, vascular and chronic), postoncologic resections (i.e., radical vulvectomy) or dermatologic disorders. The introduction in recent decades of acellular dermal matrices (ADMs) supporting the repair and restoration of skin functionality represented a significant step toward achieving clean wound repair before performing skin grafts. Hard-to-heal ulcers generally depend on local ischemia and nonadequate vascularization. In this context, one possible innovative approach could be the prevascularization of matrices with vessel-forming cells (inosculation). This paper presents a comparative analysis of the most widely used dermal templates, i.e., Integra(®) Bilayer Matrix Wound Dressing, PELNAC(®), PriMatrix(®) Dermal Repair Scaffold, Endoform(®) Natural Dermal Template, and Myriad Matrix(®), testing their ability to be colonized by human adult dermal microvascular endothelial cells (ADMECs) and to induce and support angiogenesis in vitro and in vivo. By in vitro studies, we demonstrated that Integra(®) and PELNAC(®) possess superior pro-adhesive and pro-angiogenetic properties. Animal models allowed us to demonstrate the ability of preseeded ADMECs on Integra(®) to promote the engraftment, integration and vascularization of ADMs at the site of application.
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spelling pubmed-85334492021-10-23 Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering Agostinis, Chiara Spazzapan, Mariagiulia Vuerich, Roman Balduit, Andrea Stocco, Chiara Mangogna, Alessandro Ricci, Giuseppe Papa, Giovanni Zacchigna, Serena Bulla, Roberta Biomedicines Article The loss of skin integrity has always represented a major challenge for clinicians dealing with dermal defects, such as ulcers (diabetic, vascular and chronic), postoncologic resections (i.e., radical vulvectomy) or dermatologic disorders. The introduction in recent decades of acellular dermal matrices (ADMs) supporting the repair and restoration of skin functionality represented a significant step toward achieving clean wound repair before performing skin grafts. Hard-to-heal ulcers generally depend on local ischemia and nonadequate vascularization. In this context, one possible innovative approach could be the prevascularization of matrices with vessel-forming cells (inosculation). This paper presents a comparative analysis of the most widely used dermal templates, i.e., Integra(®) Bilayer Matrix Wound Dressing, PELNAC(®), PriMatrix(®) Dermal Repair Scaffold, Endoform(®) Natural Dermal Template, and Myriad Matrix(®), testing their ability to be colonized by human adult dermal microvascular endothelial cells (ADMECs) and to induce and support angiogenesis in vitro and in vivo. By in vitro studies, we demonstrated that Integra(®) and PELNAC(®) possess superior pro-adhesive and pro-angiogenetic properties. Animal models allowed us to demonstrate the ability of preseeded ADMECs on Integra(®) to promote the engraftment, integration and vascularization of ADMs at the site of application. MDPI 2021-10-13 /pmc/articles/PMC8533449/ /pubmed/34680575 http://dx.doi.org/10.3390/biomedicines9101458 Text en © 2021 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
Agostinis, Chiara
Spazzapan, Mariagiulia
Vuerich, Roman
Balduit, Andrea
Stocco, Chiara
Mangogna, Alessandro
Ricci, Giuseppe
Papa, Giovanni
Zacchigna, Serena
Bulla, Roberta
Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title_full Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title_fullStr Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title_full_unstemmed Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title_short Differential Capability of Clinically Employed Dermal Regeneration Scaffolds to Support Vascularization for Tissue Bioengineering
title_sort differential capability of clinically employed dermal regeneration scaffolds to support vascularization for tissue bioengineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533449/
https://www.ncbi.nlm.nih.gov/pubmed/34680575
http://dx.doi.org/10.3390/biomedicines9101458
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