Native extracellular matrix: a new scaffolding platform for repair of damaged muscle
Identifieur interne : 000235 ( France/Analysis ); précédent : 000234; suivant : 000236Native extracellular matrix: a new scaffolding platform for repair of damaged muscle
Auteurs : Laura Teodori [Italie] ; Alessandra Costa [Italie, États-Unis] ; Rosa Marzio [Italie] ; Barbara Perniconi [France] ; Dario Coletti [France, Italie] ; Sergio Adamo [Italie] ; Bhuvanesh Gupta [Inde] ; Attila Tarnok [Allemagne]Source :
- Frontiers in Physiology [ 1664-042X ] ; 2014.
English descriptors
- mix :
Abstract
Effective clinical treatments for volumetric muscle loss resulting from traumatic injury or resection of a large amount of muscle mass are not available to date. Tissue engineering may represent an alternative treatment approach. Decellularization of tissues and whole organs is a recently introduced platform technology for creating scaffolding materials for tissue engineering and regenerative medicine. The muscle stem cell niche is composed of a three-dimensional architecture of fibrous proteins, proteoglycans, and glycosaminoglycans, synthesized by the resident cells that form an intricate extracellular matrix (ECM) network in equilibrium with the surrounding cells and growth factors. A consistent body of evidence indicates that ECM proteins regulate stem cell differentiation and renewal and are highly relevant to tissue engineering applications. The ECM also provides a supportive medium for blood or lymphatic vessels and for nerves. Thus, the ECM is the nature's ideal biological scaffold material. ECM-based bioscaffolds can be recellularized to create potentially functional constructs as a regenerative medicine strategy for organ replacement or tissue repopulation. This article reviews current strategies for the repair of damaged muscle using bioscaffolds obtained from animal ECM by decellularization of small intestinal submucosa (SIS), urinary bladder mucosa (UB), and skeletal muscle, and proposes some innovative approaches for the application of such strategies in the clinical setting.
Url:
DOI: 10.3389/fphys.2014.00218
PubMed: 24982637
PubMed Central: 4058757
Affiliations:
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PMC:4058757Le document en format XML
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id="aff7"><institution>Department of Pediatric Cardiology, Heart Centre Leipzig, and Translational Centre for Regenerative Medicine, University of Leipzig</institution><country>Leipzig, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea>Lineberger Comprehensive Cancer Center, University of North Carolina-Chapel Hill, Chapel Hill</wicri:regionArea><wicri:noRegion>Chapel Hill</wicri:noRegion><wicri:noRegion>Chapel Hill</wicri:noRegion><wicri:noRegion>Chapel Hill</wicri:noRegion></affiliation></author></analytic><series><title level="j">Frontiers in Physiology</title><idno type="eISSN">1664-042X</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="mix" xml:lang="en"><term>biomaterials</term><term>decellularization</term><term>extracellular matrix</term><term>regenerative medicine</term><term>scaffold</term><term>skeletal muscle</term><term>tissue engineering</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Effective clinical treatments for volumetric muscle loss resulting from traumatic injury or resection of a large amount of muscle mass are not available to date. Tissue engineering may represent an alternative treatment approach. Decellularization of tissues and whole organs is a recently introduced platform technology for creating scaffolding materials for tissue engineering and regenerative medicine. The muscle stem cell niche is composed of a three-dimensional architecture of fibrous proteins, proteoglycans, and glycosaminoglycans, synthesized by the resident cells that form an intricate extracellular matrix (ECM) network in equilibrium with the surrounding cells and growth factors. A consistent body of evidence indicates that ECM proteins regulate stem cell differentiation and renewal and are highly relevant to tissue engineering applications. The ECM also provides a supportive medium for blood or lymphatic vessels and for nerves. Thus, the ECM is the nature's ideal biological scaffold material. ECM-based bioscaffolds can be recellularized to create potentially functional constructs as a regenerative medicine strategy for organ replacement or tissue repopulation. This article reviews current strategies for the repair of damaged muscle using bioscaffolds obtained from animal ECM by decellularization of small intestinal submucosa (SIS), urinary bladder mucosa (UB), and skeletal muscle, and proposes some innovative approaches for the application of such strategies in the clinical setting.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Agrawal, V" uniqKey="Agrawal V">V. Agrawal</name></author><author><name sortKey="Brown, B N" uniqKey="Brown B">B. N. Brown</name></author><author><name sortKey="Beattie, A J" uniqKey="Beattie A">A. J. Beattie</name></author><author><name sortKey="Gilbert, T W" uniqKey="Gilbert T">T. W. Gilbert</name></author><author><name sortKey="Badylak, S F" uniqKey="Badylak S">S. F. 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Tobita</name></author><author><name sortKey="Gilbert, T W" uniqKey="Gilbert T">T. W. Gilbert</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wolf, M T" uniqKey="Wolf M">M. T. Wolf</name></author><author><name sortKey="Daly, K A" uniqKey="Daly K">K. A. Daly</name></author><author><name sortKey="Reing, J E" uniqKey="Reing J">J. E. Reing</name></author><author><name sortKey="Badylak, S F" uniqKey="Badylak S">S. F. Badylak</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wu, X" uniqKey="Wu X">X. Wu</name></author><author><name sortKey="Corona, B T" uniqKey="Corona B">B. T. Corona</name></author><author><name sortKey="Chen, X" uniqKey="Chen X">X. Chen</name></author><author><name sortKey="Walters, T J" uniqKey="Walters T">T. J. Walters</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>Allemagne</li><li>France</li><li>Inde</li><li>Italie</li><li>États-Unis</li></country></list><tree><country name="Italie"><noRegion><name sortKey="Teodori, Laura" sort="Teodori, Laura" uniqKey="Teodori L" first="Laura" last="Teodori">Laura Teodori</name></noRegion><name sortKey="Adamo, Sergio" sort="Adamo, Sergio" uniqKey="Adamo S" first="Sergio" last="Adamo">Sergio Adamo</name><name sortKey="Coletti, Dario" sort="Coletti, Dario" uniqKey="Coletti D" first="Dario" last="Coletti">Dario Coletti</name><name sortKey="Costa, Alessandra" sort="Costa, Alessandra" uniqKey="Costa A" first="Alessandra" last="Costa">Alessandra Costa</name><name sortKey="Marzio, Rosa" sort="Marzio, Rosa" uniqKey="Marzio R" first="Rosa" last="Marzio">Rosa Marzio</name><name sortKey="Teodori, Laura" sort="Teodori, Laura" uniqKey="Teodori L" first="Laura" last="Teodori">Laura Teodori</name></country><country name="États-Unis"><noRegion><name sortKey="Costa, Alessandra" sort="Costa, Alessandra" uniqKey="Costa A" first="Alessandra" last="Costa">Alessandra Costa</name></noRegion></country><country name="France"><noRegion><name sortKey="Perniconi, Barbara" sort="Perniconi, Barbara" uniqKey="Perniconi B" first="Barbara" last="Perniconi">Barbara Perniconi</name></noRegion><name sortKey="Coletti, Dario" sort="Coletti, Dario" uniqKey="Coletti D" first="Dario" last="Coletti">Dario Coletti</name></country><country name="Inde"><noRegion><name sortKey="Gupta, Bhuvanesh" sort="Gupta, Bhuvanesh" uniqKey="Gupta B" first="Bhuvanesh" last="Gupta">Bhuvanesh Gupta</name></noRegion></country><country name="Allemagne"><noRegion><name sortKey="Tarnok, Attila" sort="Tarnok, Attila" uniqKey="Tarnok A" first="Attila" last="Tarnok">Attila Tarnok</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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