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Covalent functionalization of decellularized tissues accelerates endothelialization

Authors :
Universitat Politècnica de València. Departamento de Termodinámica Aplicada - Departament de Termodinàmica Aplicada
Instituto de Salud Carlos III
Agencia Estatal de Investigación
European Regional Development Fund
Dal Sasso, Eleonora
Zamuner, Annj
Filippi, Andrea
Romanato, Filippo
Palmosi, Tiziana
Vedovelli, Luca
Gregori, Dario
Gómez Ribelles, José Luís
Russo, Teresa
Gloria, Antonio
Iop, Laura
Gerosa, Gino
Dettin, Monica
Universitat Politècnica de València. Departamento de Termodinámica Aplicada - Departament de Termodinàmica Aplicada
Instituto de Salud Carlos III
Agencia Estatal de Investigación
European Regional Development Fund
Dal Sasso, Eleonora
Zamuner, Annj
Filippi, Andrea
Romanato, Filippo
Palmosi, Tiziana
Vedovelli, Luca
Gregori, Dario
Gómez Ribelles, José Luís
Russo, Teresa
Gloria, Antonio
Iop, Laura
Gerosa, Gino
Dettin, Monica
Publication Year :
2021

Abstract

[EN] In the field of tissue regeneration, the lack of a stable endothelial lining may affect the hemocompatibility of both synthetic and biological replacements. These drawbacks might be prevented by specific biomaterial functionalization to induce selective endothelial cell (EC) adhesion. Decellularized bovine pericardia and porcine aortas were selectively functionalized with a REDV tetrapeptide at 10(-5) M and 10(-6) M working concentrations. The scaffold-bound peptide was quantified and REDV potential EC adhesion enhancement was evaluated in vitro by static seeding of human umbilical vein ECs. The viable cells and MTS production were statistically higher in functionalized tissues than in control. Scaffold histoarchitecture, geometrical features, and mechanical properties were unaffected by peptide anchoring. The selective immobilization of REDV was effective in accelerating ECs adhesion while promoting proliferation in functionalized decellularized tissues intended for blood-contacting applications.

Details

Database :
OAIster
Notes :
TEXT, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1334345513
Document Type :
Electronic Resource