2 research outputs found
Biocompatibility and immunogenicity of decellularised allogeneic aorta in the orthotopic rat model
Background and aim of the study: Peripheral arterial disease causes blood vessel dysfunction that requires surgical intervention. Current surgical interventions employ synthetic or allogeneic vascular grafts, which offer biocompatible materials solutions that are not able to regenerate or grow with the patient. Decellularised scaffolds have gained significant momentum in the past few years, since they have the potential to regenerate in the patient. The aim of this study was to investigate the effects of modified decellularisation protocol on the biocompatibility and immunogenicity of allogeneic rat abdominal aorta in an orthotopic rat model.
Methods: Native syngeneic Wistar (W) and allogeneic Dark Agouti (DA) aortas, together with decellularised allogeneic DA aortas, were assessed histologically, immunohistochemically and biomechanically. The immunogenicity of the untreated and decellularized syngeneic and allogeneic grafts was assessed in W rats, implanted orthotopically. Following implantation for 6 weeks, the grafts were explanted and assessed for the presence of T cells and macrophages by immunohistochemistry, and for their biomechanical integrity and histoarchitecture.
Results: No obvious histoarchitectural differences were observed between the native W and DA aortas, with both presenting similar three-layered structures. Histological analysis of decellularized DA aortas did not reveal any remaining cells. Explanted native DA allografts showed media necrosis, partial elastic fibre degradation and adventitia thickening, as well as infiltration by lymphocytes (CD3+, CD4+) and macrophages (CD68+) in the adventitia. The explanted decellularized DA allografts indicated reduced immune injury compared to the explanted native DA allografts. The explanted native W syngeneic grafts showed a mild immune response, with an intact media and no lymphocyte infiltration. The explanted native DA allografts showed significantly lower collagen phase slope than the decellularized DA allografts prior implantation, and significantly higher thickness than the explanted decellularized DA allografts.
Conclusions: The results indicated that the modified decellularization protocol did not affect significantly the mechanical and histological properties of the native DA rat aorta. Overall, the immune response was improved by decellularization. Native DA allografts induced an adverse immune response in W rats, whereas syngeneic W grafts showed good tissue integration
Investigation of the biomechanical integrity of decellularized rat abdominal aorta
Objectives. The loss or damage of an organ or tissue is one of the most common and
devastating problems in healthcare today. Tissue engineering applies the principles of
engineering and biology toward the development of functional biological replacements that
are able to maintain, improve, or restore the function of pathological tissues. The aim
of the overall project is to study an already existing method for the decellularization of
homograft vascular grafts for use in vascular surgery.
Materials and Methods. The biomechanical integrity of native and decellularized rat
aortas was assessed under uniaxial tension tests. For this purpose, 36 male rats (12 Wistar
and 24 Dark Agouti [DA]) were used to excise their abdominal aortas. Twelve of the aortas
were tested fresh (Wistar and DA rats), within 24 hours from euthanasia, and the rest were
decellularized using a modified protocol (DA rats only). Fresh and decellularized samples
(n ¼ 12) were subjected to uniaxial tensile loading to failure, and the recorded stress-strain
behaviour of each specimen was assessed in terms of 6 biomechanical parameters.
Results. No statistically significant differences were found in any of the biomechanical
parameters studied between the decellularized DA rat aorta group and both the native DA
and Wistar rat aorta groups (P > .05). Also, no significant difference was shown between
the native DA and native Wistar rat aorta groups.
Conclusions. The results from this study have shown that the decellularization protocol
did not affect the mechanical properties of the native rat aorta. In addition to this, both
native Wistar and native/decellularized DA rat aorta groups shared similar mechanical
properties