Author
Listed:
- Aditya Mithal
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Department of Microbiology at Boston University School of Medicine)
- Amalia Capilla
(Center for Regenerative Medicine of Boston University and Boston Medical Center)
- Dar Heinze
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Department of Surgery at Boston University School of Medicine)
- Andrew Berical
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Pulmonary Center at Boston University School of Medicine)
- Carlos Villacorta-Martin
(Center for Regenerative Medicine of Boston University and Boston Medical Center)
- Marall Vedaie
(Center for Regenerative Medicine of Boston University and Boston Medical Center)
- Anjali Jacob
(Center for Regenerative Medicine of Boston University and Boston Medical Center)
- Kristine Abo
(Center for Regenerative Medicine of Boston University and Boston Medical Center)
- Aleksander Szymaniak
(Cystic Fibrosis Foundation Therapeutics Lab)
- Megan Peasley
(Cystic Fibrosis Foundation Therapeutics Lab)
- Alexander Stuffer
(Cystic Fibrosis Foundation Therapeutics Lab)
- John Mahoney
(Cystic Fibrosis Foundation Therapeutics Lab)
- Darrell N. Kotton
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Pulmonary Center at Boston University School of Medicine)
- Finn Hawkins
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Pulmonary Center at Boston University School of Medicine)
- Gustavo Mostoslavsky
(Center for Regenerative Medicine of Boston University and Boston Medical Center
The Department of Microbiology at Boston University School of Medicine
The Section of Gastroenterology in the Department of Medicine at Boston University School of Medicine)
Abstract
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.
Suggested Citation
Aditya Mithal & Amalia Capilla & Dar Heinze & Andrew Berical & Carlos Villacorta-Martin & Marall Vedaie & Anjali Jacob & Kristine Abo & Aleksander Szymaniak & Megan Peasley & Alexander Stuffer & John , 2020.
"Generation of mesenchyme free intestinal organoids from human induced pluripotent stem cells,"
Nature Communications, Nature, vol. 11(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-13916-6
DOI: 10.1038/s41467-019-13916-6
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