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Nat Commun ; 9(1): 4286, 2018 10 16.
Article in English | MEDLINE | ID: mdl-30327457

ABSTRACT

A tissue engineered oesophagus could overcome limitations associated with oesophageal substitution. Combining decellularized scaffolds with patient-derived cells shows promise for regeneration of tissue defects. In this proof-of-principle study, a two-stage approach for generation of a bio-artificial oesophageal graft addresses some major challenges in organ engineering, namely: (i) development of multi-strata tubular structures, (ii) appropriate re-population/maturation of constructs before transplantation, (iii) cryopreservation of bio-engineered organs and (iv) in vivo pre-vascularization. The graft comprises decellularized rat oesophagus homogeneously re-populated with mesoangioblasts and fibroblasts for the muscle layer. The oesophageal muscle reaches organised maturation after dynamic culture in a bioreactor and functional integration with neural crest stem cells. Grafts are pre-vascularised in vivo in the omentum prior to mucosa reconstitution with expanded epithelial progenitors. Overall, our optimised two-stage approach produces a fully re-populated, structurally organized and pre-vascularized oesophageal substitute, which could become an alternative to current oesophageal substitutes.


Subject(s)
Esophagus/cytology , Esophagus/physiology , Muscle, Skeletal/cytology , Tissue Engineering/methods , Tissue Scaffolds , Animals , Cell Culture Techniques , Cell Differentiation , Child , Child, Preschool , Cryopreservation/methods , Epithelial Cells , Extracellular Matrix/physiology , Humans , Infant , Infant, Newborn , Male , Mice, Inbred C57BL , Mice, Transgenic , Neural Crest/transplantation , Rats, Sprague-Dawley
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