TY - JOUR
T1 - Experimental orthotopic transplantation of a tissue-engineered oesophagus in rats
AU - Sjoqvist, Sebastian
AU - Jungebluth, Philipp
AU - Ling Lim, Mei
AU - Haag, Johannes C.
AU - Gustafsson, Ylva
AU - Lemon, Greg
AU - Baiguera, Silvia
AU - Angel Burguillos, Miguel
AU - Del Gaudio, Costantino
AU - Rodríguez, Antonio Beltrán
AU - Sotnichenko, Alexander
AU - Kublickiene, Karolina
AU - Ullman, Henrik
AU - Kielstein, Heike
AU - Damberg, Peter
AU - Bianco, Alessandra
AU - Heuchel, Rainer
AU - Zhao, Ying
AU - Ribatti, Domenico
AU - Ibarra, Cristián
AU - Joseph, Bertrand
AU - Taylor, Doris A.
AU - Macchiarini, Paolo
PY - 2014
Y1 - 2014
N2 - A tissue-engineered oesophageal scaffold could be very useful for the treatment of pediatric and adult patients with benign or malignant diseases such as carcinomas, trauma or congenital malformations. Here we decellularize rat oesophagi inside a perfusion bioreactor to create biocompatible biological rat scaffolds that mimic native architecture, resist mechanical stress and induce angiogenesis. Seeded allogeneic mesenchymal stromal cells spontaneously differentiate (proven by gene-, protein and functional evaluations) into epithelial-And muscle-like cells. The reseeded scaffolds are used to orthotopically replace the entire cervical oesophagus in immunocompetent rats. All animals survive the 14-day study period, with patent and functional grafts, and gain significantly more weight than sham-operated animals. Explanted grafts show regeneration of all the major cell and tissue components of the oesophagus including functional epithelium, muscle fibres, nerves and vasculature. We consider the presented tissue-engineered oesophageal scaffolds a significant step towards the clinical application of bioengineered oesophagi.
AB - A tissue-engineered oesophageal scaffold could be very useful for the treatment of pediatric and adult patients with benign or malignant diseases such as carcinomas, trauma or congenital malformations. Here we decellularize rat oesophagi inside a perfusion bioreactor to create biocompatible biological rat scaffolds that mimic native architecture, resist mechanical stress and induce angiogenesis. Seeded allogeneic mesenchymal stromal cells spontaneously differentiate (proven by gene-, protein and functional evaluations) into epithelial-And muscle-like cells. The reseeded scaffolds are used to orthotopically replace the entire cervical oesophagus in immunocompetent rats. All animals survive the 14-day study period, with patent and functional grafts, and gain significantly more weight than sham-operated animals. Explanted grafts show regeneration of all the major cell and tissue components of the oesophagus including functional epithelium, muscle fibres, nerves and vasculature. We consider the presented tissue-engineered oesophageal scaffolds a significant step towards the clinical application of bioengineered oesophagi.
UR - http://www.scopus.com/inward/record.url?scp=84921717747&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84921717747&partnerID=8YFLogxK
U2 - 10.1038/ncomms4562
DO - 10.1038/ncomms4562
M3 - Article
C2 - 24736316
AN - SCOPUS:84921717747
SN - 2041-1723
VL - 5
JO - Nature Communications
JF - Nature Communications
M1 - 3562
ER -