TY - JOUR
T1 - Autologous induced pluripotent stem cell-derived four-organ-chip
AU - Ramme, Anja Patricia
AU - Koenig, Leopold
AU - Hasenberg, Tobias
AU - Schwenk, Christine
AU - Magauer, Corinna
AU - Faust, Daniel
AU - Lorenz, Alexandra K
AU - Krebs, Anna-Catharina
AU - Drewell, Christopher
AU - Schirrmann, Kerstin
AU - Vladetic, Alexandra
AU - Lin, Grace-Chiaen
AU - Pabinger, Stephan
AU - Neuhaus, Winfried
AU - Bois, Frederic
AU - Lauster, Roland
AU - Marx, Uwe
AU - Dehne, Eva-Maria
PY - 2019/9/10
Y1 - 2019/9/10
N2 - 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.
AB - 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.
U2 - 10.2144/fsoa-2019-0065
DO - 10.2144/fsoa-2019-0065
M3 - Article
C2 - 31534781
SN - 2056-5623
VL - 5
SP - FSO413
JO - Future science OA
JF - Future science OA
IS - 8
ER -