Generation of mesenchyme free intestinal organoids from human induced pluripotent stem cells

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作者
Aditya Mithal
Amalia Capilla
Dar Heinze
Andrew Berical
Carlos Villacorta-Martin
Marall Vedaie
Anjali Jacob
Kristine Abo
Aleksander Szymaniak
Megan Peasley
Alexander Stuffer
John Mahoney
Darrell N. Kotton
Finn Hawkins
Gustavo Mostoslavsky
机构
[1] Center for Regenerative Medicine of Boston University and Boston Medical Center,
[2] The Department of Microbiology at Boston University School of Medicine,undefined
[3] The Department of Surgery at Boston University School of Medicine,undefined
[4] The Pulmonary Center at Boston University School of Medicine,undefined
[5] Cystic Fibrosis Foundation Therapeutics Lab,undefined
[6] The Section of Gastroenterology in the Department of Medicine at Boston University School of Medicine,undefined
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摘要
Efficient generation of human induced pluripotent stem cell (hiPSC)-derived human intestinal organoids (HIOs) would facilitate the development of in vitro models for a variety of diseases that affect the gastrointestinal tract, such as inflammatory bowel disease or Cystic Fibrosis. Here, we report a directed differentiation protocol for the generation of mesenchyme-free HIOs that can be primed towards more colonic or proximal intestinal lineages in serum-free defined conditions. Using a CDX2eGFP iPSC knock-in reporter line to track the emergence of hindgut progenitors, we follow the kinetics of CDX2 expression throughout directed differentiation, enabling the purification of intestinal progenitors and robust generation of mesenchyme-free organoids expressing characteristic markers of small intestinal or colonic epithelium. We employ HIOs generated in this way to measure CFTR function using cystic fibrosis patient-derived iPSC lines before and after correction of the CFTR mutation, demonstrating their future potential for disease modeling and therapeutic screening applications.
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