Development of a primary human Small Intestine-on-a-Chip using biopsy-derived organoids

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.

[1]  Jung Keun Hyun,et al.  Three-dimensional brain-on-a-chip with an interstitial level of flow and its application as an in vitro model of Alzheimer's disease. , 2015, Lab on a chip.

[2]  Nancy L Allbritton,et al.  A microengineered collagen scaffold for generating a polarized crypt-villus architecture of human small intestinal epithelium. , 2017, Biomaterials.

[3]  Matthew E. Ritchie,et al.  limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.

[4]  Geraldine A. Hamilton,et al.  Enhanced Utilization of Induced Pluripotent Stem Cell–Derived Human Intestinal Organoids Using Microengineered Chips , 2017, Cellular and molecular gastroenterology and hepatology.

[5]  L. Griffith,et al.  A microfabricated array bioreactor for perfused 3D liver culture. , 2002, Biotechnology and bioengineering.

[6]  D. Ingber,et al.  Reconstituting Organ-Level Lung Functions on a Chip , 2010, Science.

[7]  K. Tappenden Pathophysiology of short bowel syndrome: considerations of resected and residual anatomy. , 2014, JPEN. Journal of parenteral and enteral nutrition.

[8]  M. Scarino,et al.  A protocol for in situ enzyme assays to assess the differentiation of human intestinal Caco-2 cells. , 2012, Toxicology in vitro : an international journal published in association with BIBRA.

[9]  P. Sansonetti,et al.  CD34+ mesenchymal cells are a major component of the intestinal stem cells niche at homeostasis and after injury , 2017, Proceedings of the National Academy of Sciences.

[10]  H. Kimura,et al.  An integrated microfluidic system for long-term perfusion culture and on-line monitoring of intestinal tissue models. , 2008, Lab on a chip.

[11]  Yuki Imura,et al.  A Microfluidic System to Evaluate Intestinal Absorption , 2009, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

[12]  H. Clevers,et al.  Growing Self-Organizing Mini-Guts from a Single Intestinal Stem Cell: Mechanism and Applications , 2013, Science.

[13]  Benjamin J Bondow,et al.  GATA4 is essential for jejunal function in mice. , 2008, Gastroenterology.

[14]  Nam-Trung Nguyen,et al.  Microfluidic gut-on-a-chip with three-dimensional villi structure , 2017, Biomedical microdevices.

[15]  S. Umar Intestinal Stem Cells , 2010, Current gastroenterology reports.

[16]  M. Donowitz,et al.  Functional significance of intestinal Na+-K+-ATPase: in vivo ouabain inhibition. , 1978, The American journal of physiology.

[17]  H. Daniel,et al.  Intestinal organoids for assessing nutrient transport, sensing and incretin secretion , 2015, Scientific Reports.

[18]  D. Ingber,et al.  Microfluidic organs-on-chips , 2014, Nature Biotechnology.

[19]  M. Capecchi,et al.  The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations , 2011, Proceedings of the National Academy of Sciences.

[20]  H. Clevers,et al.  Identification of stem cells in small intestine and colon by marker gene Lgr5 , 2007, Nature.

[21]  Sui Huang,et al.  Gene Expression Dynamics Inspector (GEDI): for integrative analysis of expression profiles , 2003, Bioinform..

[22]  Stephen R. Piccolo,et al.  Multiplatform single-sample estimates of transcriptional activation , 2013, Proceedings of the National Academy of Sciences.

[23]  Yan Zhou,et al.  An Intestinal Organ Culture System Uncovers a Role for the Nervous System in Microbe-Immune Crosstalk , 2017, Cell.

[24]  V. Costa,et al.  The Multifaceted Role of Annexin A1 in Viral Infections , 2023, Cells.

[25]  Sean R. Davis,et al.  NCBI GEO: archive for functional genomics data sets—update , 2012, Nucleic Acids Res..

[26]  A. Moor,et al.  Wnt Ligands Secreted by Subepithelial Mesenchymal Cells Are Essential for the Survival of Intestinal Stem Cells and Gut Homeostasis. , 2016, Cell reports.

[27]  William Stafford Noble,et al.  Analysis of strain and regional variation in gene expression in mouse brain , 2001, Genome Biology.

[28]  M. Rescigno,et al.  A novel method for the culture and polarized stimulation of human intestinal mucosa explants. , 2013, Journal of visualized experiments : JoVE.

[29]  Yoshiki Sasai,et al.  In vitro organogenesis in three dimensions: self-organising stem cells , 2012, Development.

[30]  Alex E. Lash,et al.  Gene Expression Omnibus: NCBI gene expression and hybridization array data repository , 2002, Nucleic Acids Res..

[31]  D. Ingber,et al.  Human gut-on-a-chip inhabited by microbial flora that experiences intestinal peristalsis-like motions and flow. , 2012, Lab on a chip.

[32]  N. Shanks,et al.  Are animal models predictive for humans? , 2009, Philosophy, ethics, and humanities in medicine : PEHM.

[33]  Stephen R. Piccolo,et al.  A single-sample microarray normalization method to facilitate personalized-medicine workflows. , 2012, Genomics.

[34]  G. N. Lance,et al.  Mixed-Data Classificatory Programs I - Agglomerative Systems , 1967, Aust. Comput. J..

[35]  J. Collins,et al.  Contributions of microbiome and mechanical deformation to intestinal bacterial overgrowth and inflammation in a human gut-on-a-chip , 2015, Proceedings of the National Academy of Sciences.

[36]  Donald E Ingber,et al.  Gut-on-a-Chip microenvironment induces human intestinal cells to undergo villus differentiation. , 2013, Integrative biology : quantitative biosciences from nano to macro.

[37]  Daniel C Leslie,et al.  A Human Disease Model of Drug Toxicity–Induced Pulmonary Edema in a Lung-on-a-Chip Microdevice , 2012, Science Translational Medicine.

[38]  D. Ingber,et al.  Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. , 2013, Integrative biology : quantitative biosciences from nano to macro.

[39]  Donald E Ingber,et al.  Reverse Engineering Human Pathophysiology with Organs-on-Chips , 2016, Cell.

[40]  H. Clevers,et al.  Single Lgr5 stem cells build crypt–villus structures in vitro without a mesenchymal niche , 2009, Nature.

[41]  Paul Wilmes,et al.  A microfluidics-based in vitro model of the gastrointestinal human–microbe interface , 2016, Nature Communications.

[42]  Megan L. McCain,et al.  Ensembles of engineered cardiac tissues for physiological and pharmacological study: heart on a chip. , 2011, Lab on a chip.

[43]  Kevin W Eliceiri,et al.  NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.

[44]  Teruo Fujii,et al.  Microfluidic PDMS (Polydimethylsiloxane) Bioreactor for Large‐Scale Culture of Hepatocytes , 2004, Biotechnology progress.

[45]  Laurent Griscom,et al.  Development of a Renal Microchip for In Vitro Distal Tubule Models , 2007, Biotechnology progress.

[46]  Jason R Spence,et al.  How to make an intestine , 2014, Development.

[47]  M. Elnasharty,et al.  Mucosal- Submucosal Changes in Rabbit Duodenum during Development , 2013 .

[48]  Hans Clevers,et al.  Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. , 2011, Gastroenterology.

[49]  M. Pawłowska,et al.  Light and scanning electron microscopy evaluation of the postnatal small intestinal mucosa development in pigs. , 2005, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[50]  Nick Barker,et al.  Organoids as an in vitro model of human development and disease , 2016, Nature Cell Biology.

[51]  H. Miyoshi,et al.  Development of an enhanced human gastrointestinal epithelial culture system to facilitate patient-based assays , 2014, Gut.

[52]  S. Hassan,et al.  Light and scanning electron microscopy of the small intestine of goat (Capra hircus) , 2015 .

[53]  Kevin W. Eliceiri,et al.  ImageJ2: ImageJ for the next generation of scientific image data , 2017, BMC Bioinformatics.

[54]  M. Toner,et al.  Effects of oxygenation and flow on the viability and function of rat hepatocytes cocultured in a microchannel flat-plate bioreactor. , 2001, Biotechnology and bioengineering.

[55]  Umair Aslam,et al.  Meta-Analysis of the Turnover of Intestinal Epithelia in Preclinical Animal Species and Humans , 2014, Drug Metabolism and Disposition.

[56]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.