TY - JOUR
T1 - Development of a primary human Small Intestine-on-a-Chip using biopsy-derived organoids
AU - Kasendra, Magdalena
AU - Tovaglieri, Alessio
AU - Sontheimer-Phelps, Alexandra
AU - Jalili-Firoozinezhad, Sasan
AU - Bein, Amir
AU - Chalkiadaki, Angeliki
AU - Scholl, William
AU - Zhang, Cheng
AU - Rickner, Hannah
AU - Richmond, Camilla A.
AU - Li, Hu
AU - Breault, David T.
AU - Ingber, Donald E.
N1 - Funding Information:
This work was funded by DARPA (contract W911NF-12-2-0036), FDA grant HHSF223201310079C, the Ragon Institute of MGH, MIT and Harvard, the Bill and Melinda Gates Foundation, and the Wyss Institute for Biologically Inspired Engineering at Harvard University (to D.E.I.). The production of human organoids was supported by NIH grants F32DK091995, T32DK007477, 5K12HD5289610, HMS Shore Fellowship, BCH Wolpow/Rubin IBD Fellowship, NASPGHAN Nestl Nutrition Award, and HDDC Pilot & Feasibility Award (to C.A.R.), R01DK084056, the Timothy Murphy Fund, the IDDRC P30HD18655 and the HDDC P30DK034854 (to D.T.B.). We thank K. Karalis and G. Hamilton for their help initiating this project; A. Monreal, O. Levy, and R. Prantil-Baun for their expert advice; and P. Praveschotinunt for assistance with SEM imaging.
Funding Information:
This work was funded by DARPA (contract W911NF-12-2-0036), FDA grant HHSF223201310079C, the Ragon Institute of MGH, MIT and Harvard, the Bill and Melinda Gates Foundation, and the Wyss Institute for Biologically Inspired Engineering at Harvard University (to D.E.I.). The production of human organoids was supported by NIH grants F32DK091995, T32DK007477, 5K12HD5289610, HMS Shore Fellowship, BCH Wolpow/Rubin IBD Fellowship, NASPGHAN Nestlé Nutrition Award, and HDDC Pilot & Feasibility Award (to C.A.R.), R01DK084056, the Timothy Murphy Fund, the IDDRC P30HD18655 and the HDDC P30DK034854 (to D.T.B.). We thank K. Karalis and G. Hamilton for their help initiating this project; A. Monreal, O. Levy, and R. Prantil-Baun for their expert advice; and P. Praveschotinunt for assistance with SEM imaging.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Here we describe a method for fabricating a primary human Small Intestine-on-a-Chip (Intestine Chip) containing epithelial cells isolated from healthy regions of intestinal biopsies. The primary epithelial cells are expanded as 3D organoids, dissociated, and cultured on a porous membrane within a microfluidic device with human intestinal microvascular endothelium cultured in a parallel microchannel under flow and cyclic deformation. In the Intestine Chip, the epithelium forms villi-like projections lined by polarized epithelial cells that undergo multi-lineage differentiation similar to that of intestinal organoids, however, these cells expose their apical surfaces to an open lumen and interface with endothelium. Transcriptomic analysis also indicates that the Intestine Chip more closely mimics whole human duodenum in vivo when compared to the duodenal organoids used to create the chips. Because fluids flowing through the lumen of the Intestine Chip can be collected continuously, sequential analysis of fluid samples can be used to quantify nutrient digestion, mucus secretion and establishment of intestinal barrier function over a period of multiple days in vitro. The Intestine Chip therefore may be useful as a research tool for applications where normal intestinal function is crucial, including studies of metabolism, nutrition, infection, and drug pharmacokinetics, as well as personalized medicine.
AB - Here we describe a method for fabricating a primary human Small Intestine-on-a-Chip (Intestine Chip) containing epithelial cells isolated from healthy regions of intestinal biopsies. The primary epithelial cells are expanded as 3D organoids, dissociated, and cultured on a porous membrane within a microfluidic device with human intestinal microvascular endothelium cultured in a parallel microchannel under flow and cyclic deformation. In the Intestine Chip, the epithelium forms villi-like projections lined by polarized epithelial cells that undergo multi-lineage differentiation similar to that of intestinal organoids, however, these cells expose their apical surfaces to an open lumen and interface with endothelium. Transcriptomic analysis also indicates that the Intestine Chip more closely mimics whole human duodenum in vivo when compared to the duodenal organoids used to create the chips. Because fluids flowing through the lumen of the Intestine Chip can be collected continuously, sequential analysis of fluid samples can be used to quantify nutrient digestion, mucus secretion and establishment of intestinal barrier function over a period of multiple days in vitro. The Intestine Chip therefore may be useful as a research tool for applications where normal intestinal function is crucial, including studies of metabolism, nutrition, infection, and drug pharmacokinetics, as well as personalized medicine.
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U2 - 10.1038/s41598-018-21201-7
DO - 10.1038/s41598-018-21201-7
M3 - Article
C2 - 29440725
AN - SCOPUS:85042054523
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 2871
ER -