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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6745596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
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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