Isogenic human-induced Pluripotent Stem Cell- derived liver cells from healthy and diseased donors: A valuable tool for modeling inflammation and fibrosis
- Datum
- 22.09.2023
- Zeit
- 11:00 - 12:00
- Sprecher
- Aina, Kehinde O.
- Zugehörigkeit
- Marie Curie Sklodowska Fellow, INSPIRE research group, Uniklinikum Jena
- Sprache
- en
- Hauptthema
- Biologie
- Host
- Meritxell Huch
- Beschreibung
- To improve the predictive power of in vitro models, vascular biology needs to be integrated into a functional, preferably facile, technology. The use of human induced pluripotent stem cells (hiPSC) in combination with micro-physiological systems, have emerged as tools to provide insight into the mechanisms of metabolic liver disorders, and liver fibrosis. A novel on-chip in vitro differentiation and tissue engineering procedure was used to generate a stem cell-based derived liver-on-chip model using a hiPSC panel of healthy and NASH donors in a 3D format. Liver fibrosis disease modeling was based on the stimulation of the model with transforming growth factor β. The fibrosis phenotype was validated based on endothelial cell dysfunction, stellate cell activation, and deposition of extracellular matrix. Isogenic LoC models would facilitate the study of patho-physiological processes involved in liver disease progression for personalized medicine approaches.
Letztmalig verändert: 23.09.2023, 07:35:33
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Max Planck Institute of Molecular Cell Biology and GeneticsPfotenhauerstraße10801307Dresden
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- +49 351 210-0
- Fax
- +49 351 210-2000
- MPI-CBG
- Homepage
- http://www.mpi-cbg.de
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