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Autologous induced pluripotent stem cell-derived four-organ-chip

Microphysiological systems play a pivotal role in progressing toward a global paradigm shift in drug development. Here, we designed a four-organ-chip interconnecting miniaturized human intestine, liver, brain and kidney equivalents. All four organ models were predifferentiated from induced pluripote...

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Autores principales: Ramme, Anja Patricia, Koenig, Leopold, Hasenberg, Tobias, Schwenk, Christine, Magauer, Corinna, Faust, Daniel, Lorenz, Alexandra K, Krebs, Anna-Catharina, Drewell, Christopher, Schirrmann, Kerstin, Vladetic, Alexandra, Lin, Grace-Chiaen, Pabinger, Stephan, Neuhaus, Winfried, Bois, Frederic, Lauster, Roland, Marx, Uwe, Dehne, Eva-Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745596/
https://www.ncbi.nlm.nih.gov/pubmed/31534781
http://dx.doi.org/10.2144/fsoa-2019-0065
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author Ramme, Anja Patricia
Koenig, Leopold
Hasenberg, Tobias
Schwenk, Christine
Magauer, Corinna
Faust, Daniel
Lorenz, Alexandra K
Krebs, Anna-Catharina
Drewell, Christopher
Schirrmann, Kerstin
Vladetic, Alexandra
Lin, Grace-Chiaen
Pabinger, Stephan
Neuhaus, Winfried
Bois, Frederic
Lauster, Roland
Marx, Uwe
Dehne, Eva-Maria
author_facet Ramme, Anja Patricia
Koenig, Leopold
Hasenberg, Tobias
Schwenk, Christine
Magauer, Corinna
Faust, Daniel
Lorenz, Alexandra K
Krebs, Anna-Catharina
Drewell, Christopher
Schirrmann, Kerstin
Vladetic, Alexandra
Lin, Grace-Chiaen
Pabinger, Stephan
Neuhaus, Winfried
Bois, Frederic
Lauster, Roland
Marx, Uwe
Dehne, Eva-Maria
author_sort Ramme, Anja Patricia
collection PubMed
description Microphysiological systems play a pivotal role in progressing toward a global paradigm shift in drug development. Here, we designed a four-organ-chip interconnecting miniaturized human intestine, liver, brain and kidney equivalents. All four organ models were predifferentiated from induced pluripotent stem cells from the same healthy donor and integrated into the microphysiological system. The coculture of the four autologous tissue models in one common medium deprived of tissue specific growth factors was successful over 14-days. Although there were no added growth factors present in the coculture medium, the intestine, liver and neuronal model maintained defined marker expression. Only the renal model was overgrown by coexisting cells and did not further differentiate. This model platform will pave the way for autologous coculture cross-talk assays, disease induction and subsequent drug testing.
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spelling pubmed-67455962019-09-18 Autologous induced pluripotent stem cell-derived four-organ-chip Ramme, Anja Patricia Koenig, Leopold Hasenberg, Tobias Schwenk, Christine Magauer, Corinna Faust, Daniel Lorenz, Alexandra K Krebs, Anna-Catharina Drewell, Christopher Schirrmann, Kerstin Vladetic, Alexandra Lin, Grace-Chiaen Pabinger, Stephan Neuhaus, Winfried Bois, Frederic Lauster, Roland Marx, Uwe Dehne, Eva-Maria Future Sci OA Methodology Microphysiological systems play a pivotal role in progressing toward a global paradigm shift in drug development. Here, we designed a four-organ-chip interconnecting miniaturized human intestine, liver, brain and kidney equivalents. All four organ models were predifferentiated from induced pluripotent stem cells from the same healthy donor and integrated into the microphysiological system. The coculture of the four autologous tissue models in one common medium deprived of tissue specific growth factors was successful over 14-days. Although there were no added growth factors present in the coculture medium, the intestine, liver and neuronal model maintained defined marker expression. Only the renal model was overgrown by coexisting cells and did not further differentiate. This model platform will pave the way for autologous coculture cross-talk assays, disease induction and subsequent drug testing. Future Science Ltd 2019-09-10 /pmc/articles/PMC6745596/ /pubmed/31534781 http://dx.doi.org/10.2144/fsoa-2019-0065 Text en © 2019 TissUse GmbH This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Methodology
Ramme, Anja Patricia
Koenig, Leopold
Hasenberg, Tobias
Schwenk, Christine
Magauer, Corinna
Faust, Daniel
Lorenz, Alexandra K
Krebs, Anna-Catharina
Drewell, Christopher
Schirrmann, Kerstin
Vladetic, Alexandra
Lin, Grace-Chiaen
Pabinger, Stephan
Neuhaus, Winfried
Bois, Frederic
Lauster, Roland
Marx, Uwe
Dehne, Eva-Maria
Autologous induced pluripotent stem cell-derived four-organ-chip
title Autologous induced pluripotent stem cell-derived four-organ-chip
title_full Autologous induced pluripotent stem cell-derived four-organ-chip
title_fullStr Autologous induced pluripotent stem cell-derived four-organ-chip
title_full_unstemmed Autologous induced pluripotent stem cell-derived four-organ-chip
title_short Autologous induced pluripotent stem cell-derived four-organ-chip
title_sort autologous induced pluripotent stem cell-derived four-organ-chip
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745596/
https://www.ncbi.nlm.nih.gov/pubmed/31534781
http://dx.doi.org/10.2144/fsoa-2019-0065
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