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      Análise do comportamento biológico de heteroenxertos descelularizados e homoenxertos criopreservados: estudo em ovinos Translated title: Decellularized heterografts versus cryopreserved homografts: experimental study in sheep model

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          Abstract

          OBJETIVO: Este estudo avalia o comportamento biológico dos heteroenxertos porcinos descelularizados (Grupo Desc) comparados com os homoenxertos criopreservados (Grupo Crio) implantados em carneiros jovens. MÉTODOS: Foram implantados em cinco animais heteroenxertos pulmonares porcinos descelularizados e em outros cinco, homoenxertos pulmonares criopreservados. Os animais apresentaram seguimento médio de 280 ± 14 dias. O diâmetro valvar foi medido por ecocardiografia, a qual foi realizada no 30º pós-operatório e antes do explante. As valvas foram também avaliadas macroscopicamente. A avaliação histológica foi realizada utilizando-se coloração de H.E., Gomori e Weigert e imunohistoquímica (Fator VIII, CD3, Vimentina e CD68). A quantificação de cálcio foi realizada utilizando-se espectrometria de absorção atômica. RESULTADOS: Houve um óbito no Grupo Desc por endocardite. As valvas do Grupo Crio apresentaram decréscimo na celularidade, enquanto que as valvas do Grupo Desc demonstraram repovoamento da matriz com células endoteliais e intersticiais. No grupo Crio, observou-se perda na densidade e desarranjo da arquitetura das fibras colágenas. A espectrometria de absorção atômica demonstrou maior calcificação no conduto e nas cúspides dos enxertos criopreservados quando comparados aos descelularizados (P=0,016). O diâmetro médio valvar no explante foi significantemente maior no Grupo Desc (P=0,025). CONCLUSÃO: Heteroenxertos descelularizados apresentam um comportamento biológico diferente quando comparados aos homoenxertos criopreservados, tornando-se repovoados por células com características de fibroblastos e células endoteliais. A matriz permaneceu bem preservada, o que possibilitou um processo de regeneração celular.

          Translated abstract

          OBJECTIVES: The aim of this study is to assess the biological behaviour of porcine decellularized heterografts (Desc group) compared with cryopreserved homografts (Crio group) implanted in juvenile sheep. METHODS: Decellularized porcine pulmonary heterografts were implanted in five animals and cryopreserved pulmonary homografts in another five. The animals were followed-up for a mean of 280 ± 14 days. The valve diameter was measured by echocardiography, which was performed at the 30th postoperative day, and before the explantation. The valves were also assessed macroscopically. Histological evaluation was performed using H.E., Gomori and Weigert staining. Immunohistochemistry specified different cell types (Factor VIII, CD3, Vimentin and CD68). Calcium quantity was analyzed using atomic absortion spectometry. RESULTS: There was one death in the Desc group due to endocarditis. The valves of Crio group showed decrease in the cellularity whereas the valves of Desc group showed matrix repopulation with endothelial and interstitial cells. Loss of collagen density and disarrangement of the normal fiber architecture was observed in Crio group. Calcium content demonstrated higher levels on the cusps and conduits in Crio group comparatively with Desc group. (P=0.016). The mean valvular diameter at the explantation was significantly increased (P=0.025) in the Desc group. CONCLUSIONS: Decellularized heterografts had a different biological behaviour when compared to cryopreserved homografts and become repopulated by cells with fibroblasts and endothelial cells characteristics. The matrix was preserved and some regenerative potential was present

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          Histological evaluation of decellularised porcine aortic valves: matrix changes due to different decellularisation methods.

          Several decellularisation techniques have been developed to produce acellular matrix scaffolds for the purpose of tissue engineering, mostly comprising (non-)ionic detergents or enzymatic extraction methods. However, the effect of chemically induced decellularisation on the major structural and adhesion molecules as well as glycosaminoglycans, and the possible replenishment of lost compounds have escaped attention. Porcine aortic valves were treated with two different methods: detergent Triton X-100 and enzymatic Trypsine cell extraction. (Immuno-) histochemistry was used to address changes in extracellular matrix constitution (elastin, collagen, glycosaminoglycans, chondroitin sulfate, fibronectin and laminin) and the production of extracellular matrix components by seeded endothelial cells. The Trypsine treated group showed a fragmentation and distortion of elastic fibers. Changes in collagen distribution were observed in both groups. An almost complete washout of glycosaminoglycans and chondroitin sulfate was observed in the Triton and Trypsin treated group, but the latter with a smaller glycosaminoglycans reduction. Both treatments resulted in a considerable washout of the adhesion molecules laminin and fibronectin. Furthermore, seeded endothelial cells were capable of synthesising laminin, fibronectin and chondroitin sulfate. Chemically induced decellularisation by Triton or Trypsine resulted in changes in the extracellular matrix constitution, which could lead to problems in valve functionality and cell growth and migration. Seeded endothelial cells were capable of synthesising extracellular matrix components lost by cell extraction. Further studies on tissue engineering should focus more on the effect of chemically induced cell extraction on the extracellular matrix of the remaining scaffold and the in vitro or in vivo replenishment of lost compounds.
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            Tissue engineering of pulmonary heart valves on allogenic acellular matrix conduits: in vivo restoration of valve tissue.

            Tissue engineering using in vitro-cultivated autologous vascular wall cells is a new approach to biological heart valve replacement. In the present study, we analyzed a new concept to process allogenic acellular matrix scaffolds of pulmonary heart valves after in vitro seeding with the use of autologous cells in a sheep model. Allogenic heart valve conduits were acellularized by a 48-hour trypsin/EDTA incubation to extract endothelial cells and myofibroblasts. The acellularization procedure resulted in an almost complete removal of cells. After that procedure, a static reseeding of the upper surface of the valve was performed sequentially with autologous myofibroblasts for 6 days and endothelial cells for 2 days, resulting in a patchy cellular restitution on the valve surface. The in vivo function was tested in a sheep model of orthotopic pulmonary valve conduit transplantation. Three of 4 unseeded control valves and 5 of 6 tissue-engineered valves showed normal function up to 3 months. Unseeded allogenic acellular control valves showed partial degeneration (2 of 4 valves) and no interstitial valve tissue reconstitution. Tissue-engineered valves showed complete histological restitution of valve tissue and confluent endothelial surface coverage in all cases. Immunohistological analysis revealed cellular reconstitution of endothelial cells (von Willebrand factor), myofibroblasts (alpha-actin), and matrix synthesis (procollagen I). There were histological signs of inflammatory reactions to subvalvar muscle leading to calcifications, but these were not found in valve and pulmonary artery tissue. The in vitro tissue-engineering approach using acellular matrix conduits leads to the in vivo reconstitution of viable heart valve tissue.
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              Tissue engineering of heart valves – human endothelial cell seeding of detergent acellularized porcine valves1

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                Author and article information

                Journal
                rbccv
                Brazilian Journal of Cardiovascular Surgery
                Braz. J. Cardiovasc. Surg.
                Sociedade Brasileira de Cirurgia Cardiovascular (São Paulo, SP, Brazil )
                0102-7638
                1678-9741
                March 2009
                : 24
                : 1
                : 15-22
                Affiliations
                [01] Berlim orgnameHospital Charité
                [02] orgnamePUC-PR
                Article
                S0102-76382009000100005 S0102-7638(09)02400105
                7b8a2d2a-ce63-4093-b2fa-4b95aeebb2ee

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 09 September 2008
                : 16 January 2009
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 17, Pages: 8
                Categories
                Artigos Originais

                Criopreservação,Engenharia de tecidos,Transplantation, homologous,Transplantation, heterologous,Cryopreservation,Tissue engeneering,Transplante homólogo,Transplante heterólogo

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