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Updated: Jul 18, 2026
Transcatheter Pulmonary Valve Replacement from Autologous Pericardium with a Self-Expandable Nitinol Stent in an Adult Sheep Model
Published on: June 8, 2022
Histological evaluation of tissue-engineered heart valves implanted in the juvenile sheep model: is there a need for
Pascal M Dohmen1, Francisco da Costa, Sergio Yoshi
1Department of Cardiovascular Surgery, Charité Hospital, Medical University Berlin, Berlin, Germany. pascal.dohmen@charite.de
Background And Aim Of The Study:
A new-generation heart valve was developed to improve long-term durability. The study aim was to evaluate the need for in-vitro autologous endothelial cell seeding of a decellularized valve scaffold.
Methods:
A seeded (group I, n = 6) or non-seeded (group II, n=6) decellularized valve was implanted into the right ventricular outflow tract of 12 juvenile sheep. In group I, a jugular vein was harvested to characterize and expand endothelial cells (ECs). The scaffold was seeded in vitro, using a sedimentation technique. In group II, non-seeded decellularized scaffolds were implanted and explantation was performed at three and six months. Valves were evaluated by echocardiography, gross pathology, X-radiography, histology, and immunohistochemistry.
Results:
In group I, the EC seeding density was 1.06 +/- 0.01 x 10(5) cells/cm2, with a cell viability of 95.7 +/- 1.4%. No regurgitation was visualized by echocardiography. Gross pathology showed smooth leaflets without retraction; calcification was absent at X-radiography, and this was confirmed by von Kossa staining. Histologically, group I valves showed a persistence of ECs, whereas a monolayer of host ECs was seen at six months in group II valves. Host fibroblasts were available in both groups, and numbers increased over time. Differences were identified in the recellularization density of in-vitro-seeded and non-seeded valves for up to three months, but no such difference was seen after six months.
Conclusion:
Based on results of studies in a sheep model, there appears to be no need for in-vitro cell seeding of decellularized scaffolds.
