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1.
Cell Tissue Bank ; 25(1): 43-53, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37138137

RESUMO

More than 1000 donated aortic and pulmonary valves from predominantly European tissue banks were centrally decellularized and delivered to hospitals in Europe and Japan. Here, we report on the processing and quality controls before, during and after the decellularization of these allografts. Our experiences show that all tissue establishments, which provide native cardiovascular allografts for decellularization, meet comparably high-quality standards, regardless of their national origin. A total of 84% of all received allografts could be released as cell-free allografts. By far the most frequent reasons for rejection were non-release of the donor by the tissue establishment or severe contaminations of the native tissue donation. Only in 2% of all cases the specification for freedom from cells was not fulfilled, indicating that decellularization of human heart valves is a safe process with a very low discard ratio. In clinical use, cell-free cardiovascular allografts have been shown to be advantageous over conventional heart valve replacements, at least in young adults. These results open the discussion on the future gold standard and funding of this innovative therapeutic option for heart valve replacement.


Assuntos
Valvas Cardíacas , Valva Pulmonar , Adulto Jovem , Humanos , Transplante Homólogo , Doadores de Tecidos , Controle de Qualidade
2.
Stem Cell Res ; 40: 101542, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31473565

RESUMO

CFTR encodes for a chloride ion channel expressed primarily in secretory epithelia in the airways, intestine, liver and other tissues. Mutations in the CFTR gene have been identified in people suffering from Cystic Fibrosis. Here, we established a CFTR knock-in reporter cell line from a human iPSC line (MHHi006-A) using TALEN technology. The reporter enables the monitoring and optimization of the differentiation of pluripotent stem cells into CFTR expressing epithelia on a single cell level, as well as the enrichment of CFTR positive cells, which represent an excellent tool for Cystic Fibrosis disease modelling, drug screening and ultimately cellular therapies.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Edição de Genes , Células-Tronco Pluripotentes Induzidas/citologia , Potenciais de Ação/efeitos dos fármacos , Diferenciação Celular , Linhagem Celular , Reprogramação Celular , Colforsina/farmacologia , Humanos , Células-Tronco Pluripotentes Induzidas/metabolismo , Cariótipo , Masculino , Nucleases dos Efetores Semelhantes a Ativadores de Transcrição/genética
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