TY - JOUR
T1 - Decellularized esophageal tubular scaffold microperforated by quantum molecular resonance technology and seeded with mesenchymal stromal cells for tissue engineering esophageal regeneration
AU - Marzaro, Maurizio
AU - Pozzato, Gianantonio
AU - Tedesco, Stefano
AU - Algeri, Mattia
AU - Pozzato, Alessandro
AU - Tomao, Luigi
AU - Montano, Ilaria
AU - Torroni, Filippo
AU - Balassone, Valerio
AU - Contini, Anna Chiara Iolanda
AU - Guerra, Luciano
AU - D’Angelo, Tommaso
AU - Federici Di Abriola, Giovanni
AU - Lupoi, Lorenzo
AU - Caristo, Maria Emiliana
AU - Boskoski, Ivo
AU - Costamagna, Guido
AU - Francalanci, Paola
AU - Astori, Giuseppe
AU - Bozza, Angela
AU - Bagno, Andrea
AU - Todesco, Martina
AU - Trovalusci, Emanuele
AU - Oglio, Luigi Dall’
AU - Dall'Oglio, Luigi
AU - Locatelli, Franco
AU - Caldaro, Tamara
PY - 2022
Y1 - 2022
N2 - Current surgical options for patients requiring esophageal replacement suffer from several limitations and do not assure a satisfactory quality of life. Tissue engineering techniques for the creation of customized "self-developing" esophageal substitutes, which are obtained by seeding autologous cells on artificial or natural scaffolds, allow simplifying surgical procedures and achieving good clinical outcomes. In this context, an appealing approach is based on the exploitation of decellularized tissues as biological matrices to be colonized by the appropriate cell types to regenerate the desired organs. With specific regard to the esophagus, the presence of a thick connective texture in the decellularized scaffold hampers an adequate penetration and spatial distribution of cells. In the present work, the Quantum Molecular Resonance (R) (QMR) technology was used to create a regular microchannel structure inside the connective tissue of full-thickness decellularized tubular porcine esophagi to facilitate a diffuse and uniform spreading of seeded mesenchymal stromal cells within the scaffold. Esophageal samples were thoroughly characterized before and after decellularization and microperforation in terms of residual DNA content, matrix composition, structure and biomechanical features. The scaffold was seeded with mesenchymal stromal cells under dynamic conditions, to assess the ability to be repopulated before its implantation in a large animal model. At the end of the procedure, they resemble the original esophagus, preserving the characteristic multilayer composition and maintaining biomechanical properties adequate for surgery. After the sacrifice we had histological and immunohistochemical evidence of the full-thickness regeneration of the esophageal wall, resembling the native organ. These results suggest the QMR microperforated decellularized esophageal scaffold as a promising device for esophagus regeneration in patients needing esophageal substitution.
AB - Current surgical options for patients requiring esophageal replacement suffer from several limitations and do not assure a satisfactory quality of life. Tissue engineering techniques for the creation of customized "self-developing" esophageal substitutes, which are obtained by seeding autologous cells on artificial or natural scaffolds, allow simplifying surgical procedures and achieving good clinical outcomes. In this context, an appealing approach is based on the exploitation of decellularized tissues as biological matrices to be colonized by the appropriate cell types to regenerate the desired organs. With specific regard to the esophagus, the presence of a thick connective texture in the decellularized scaffold hampers an adequate penetration and spatial distribution of cells. In the present work, the Quantum Molecular Resonance (R) (QMR) technology was used to create a regular microchannel structure inside the connective tissue of full-thickness decellularized tubular porcine esophagi to facilitate a diffuse and uniform spreading of seeded mesenchymal stromal cells within the scaffold. Esophageal samples were thoroughly characterized before and after decellularization and microperforation in terms of residual DNA content, matrix composition, structure and biomechanical features. The scaffold was seeded with mesenchymal stromal cells under dynamic conditions, to assess the ability to be repopulated before its implantation in a large animal model. At the end of the procedure, they resemble the original esophagus, preserving the characteristic multilayer composition and maintaining biomechanical properties adequate for surgery. After the sacrifice we had histological and immunohistochemical evidence of the full-thickness regeneration of the esophageal wall, resembling the native organ. These results suggest the QMR microperforated decellularized esophageal scaffold as a promising device for esophagus regeneration in patients needing esophageal substitution.
KW - esophagus
KW - mesenchymal stromal cells
KW - quantum molecular resonance
KW - scaffold
KW - tissue engineering
KW - esophagus
KW - mesenchymal stromal cells
KW - quantum molecular resonance
KW - scaffold
KW - tissue engineering
UR - http://hdl.handle.net/10807/221716
U2 - 10.3389/fbioe.2022.912617
DO - 10.3389/fbioe.2022.912617
M3 - Article
SN - 2296-4185
VL - 10
SP - 912617-N/A
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
ER -