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Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle

BACKGROUND: Tissue engineering of vascularised skeletal muscle is a promising method for the treatment of soft tissue defects in reconstructive surgery. In this study we explored the characteristics of novel collagen and fibrin matrices for skeletal muscle tissue engineering. We analyzed the charact...

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Autores principales: Beier, Justus P, Klumpp, Dorothee, Rudisile, Markus, Dersch, Roland, Wendorff, Joachim H, Bleiziffer, Oliver, Arkudas, Andreas, Polykandriotis, Elias, Horch, Raymund E, Kneser, Ulrich
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2674407/
https://www.ncbi.nlm.nih.gov/pubmed/19368709
http://dx.doi.org/10.1186/1472-6750-9-34
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author Beier, Justus P
Klumpp, Dorothee
Rudisile, Markus
Dersch, Roland
Wendorff, Joachim H
Bleiziffer, Oliver
Arkudas, Andreas
Polykandriotis, Elias
Horch, Raymund E
Kneser, Ulrich
author_facet Beier, Justus P
Klumpp, Dorothee
Rudisile, Markus
Dersch, Roland
Wendorff, Joachim H
Bleiziffer, Oliver
Arkudas, Andreas
Polykandriotis, Elias
Horch, Raymund E
Kneser, Ulrich
author_sort Beier, Justus P
collection PubMed
description BACKGROUND: Tissue engineering of vascularised skeletal muscle is a promising method for the treatment of soft tissue defects in reconstructive surgery. In this study we explored the characteristics of novel collagen and fibrin matrices for skeletal muscle tissue engineering. We analyzed the characteristics of newly developed hybrid collagen-I-fibrin-gels and collagen nanofibers as well as collagen sponges and OPLA(®)-scaffolds. Collagen-fibrin gels were also tested with genipin as stabilizing substitute for aprotinin. RESULTS: Whereas rapid lysis and contraction of pure collagen I- or fibrin-matrices have been great problems in the past, the latter could be overcome by combining both materials. Significant proliferation of cultivated myoblasts was detected in collagen-I-fibrin matrices and collagen nanofibers. Seeding cells on parallel orientated nanofibers resulted in strongly aligned myoblasts. In contrast, common collagen sponges and OPLA(®)-scaffolds showed less cell proliferation and in collagen sponges an increased apoptosis rate was evident. The application of genipin caused deleterious effects on primary myoblasts. CONCLUSION: Collagen I-fibrin mixtures as well as collagen nanofibers yield good proliferation rates and myogenic differentiation of primary rat myoblasts in vitro In addition, parallel orientated nanofibers enable the generation of aligned cell layers and therefore represent the most promising step towards successful engineering of skeletal muscle tissue.
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spelling pubmed-26744072009-04-29 Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle Beier, Justus P Klumpp, Dorothee Rudisile, Markus Dersch, Roland Wendorff, Joachim H Bleiziffer, Oliver Arkudas, Andreas Polykandriotis, Elias Horch, Raymund E Kneser, Ulrich BMC Biotechnol Research Article BACKGROUND: Tissue engineering of vascularised skeletal muscle is a promising method for the treatment of soft tissue defects in reconstructive surgery. In this study we explored the characteristics of novel collagen and fibrin matrices for skeletal muscle tissue engineering. We analyzed the characteristics of newly developed hybrid collagen-I-fibrin-gels and collagen nanofibers as well as collagen sponges and OPLA(®)-scaffolds. Collagen-fibrin gels were also tested with genipin as stabilizing substitute for aprotinin. RESULTS: Whereas rapid lysis and contraction of pure collagen I- or fibrin-matrices have been great problems in the past, the latter could be overcome by combining both materials. Significant proliferation of cultivated myoblasts was detected in collagen-I-fibrin matrices and collagen nanofibers. Seeding cells on parallel orientated nanofibers resulted in strongly aligned myoblasts. In contrast, common collagen sponges and OPLA(®)-scaffolds showed less cell proliferation and in collagen sponges an increased apoptosis rate was evident. The application of genipin caused deleterious effects on primary myoblasts. CONCLUSION: Collagen I-fibrin mixtures as well as collagen nanofibers yield good proliferation rates and myogenic differentiation of primary rat myoblasts in vitro In addition, parallel orientated nanofibers enable the generation of aligned cell layers and therefore represent the most promising step towards successful engineering of skeletal muscle tissue. BioMed Central 2009-04-15 /pmc/articles/PMC2674407/ /pubmed/19368709 http://dx.doi.org/10.1186/1472-6750-9-34 Text en Copyright © 2009 Beier et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Beier, Justus P
Klumpp, Dorothee
Rudisile, Markus
Dersch, Roland
Wendorff, Joachim H
Bleiziffer, Oliver
Arkudas, Andreas
Polykandriotis, Elias
Horch, Raymund E
Kneser, Ulrich
Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title_full Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title_fullStr Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title_full_unstemmed Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title_short Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
title_sort collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2674407/
https://www.ncbi.nlm.nih.gov/pubmed/19368709
http://dx.doi.org/10.1186/1472-6750-9-34
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