Establishment of Gastrointestinal Epithelial Organoids
Maxime M. Mahe
Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
These authors contributed equally to this work
Search for more papers by this authorEitaro Aihara
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
These authors contributed equally to this work
Search for more papers by this authorMichael A. Schumacher
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorYana Zavros
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorMarshall H. Montrose
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorMichael A. Helmrath
Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
Search for more papers by this authorToshiro Sato
Department of Gastroenterology, School of Medicine, Keio University, Tokyo, Japan
Search for more papers by this authorNoah F. Shroyer
Division of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
Search for more papers by this authorMaxime M. Mahe
Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
These authors contributed equally to this work
Search for more papers by this authorEitaro Aihara
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
These authors contributed equally to this work
Search for more papers by this authorMichael A. Schumacher
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorYana Zavros
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorMarshall H. Montrose
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio
Search for more papers by this authorMichael A. Helmrath
Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
Search for more papers by this authorToshiro Sato
Department of Gastroenterology, School of Medicine, Keio University, Tokyo, Japan
Search for more papers by this authorNoah F. Shroyer
Division of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio
Search for more papers by this authorAbstract
The intestinal epithelium constitutes a system of constant and rapid renewal triggered by proliferation of intestinal stem cells (ISCs), and is an ideal system for studying cell proliferation, migration, and differentiation. Primary cell cultures have proven to be promising for unraveling the mechanisms involved in epithelium homeostasis. In 2009, Sato et al. established a long-term primary culture to generate epithelial organoids (enteroids) with crypt- and villus-like epithelial domains representing the complete census of progenitors and differentiated cells. Similarly, isolated ISCs expressing Lgr5 (leucine-rich repeat-containing G protein–coupled receptor) can generate enteroids. Here, we describe methods to establish gastric, small intestinal, and colonic epithelial organoids and generate Lgr5+ve single cell–derived epithelial organoids. We also describe the imaging techniques used to characterize those organoids. This in vitro model constitutes a powerful tool for studying stem cell biology and intestinal epithelial cell physiology throughout the digestive tract. Curr. Protoc. Mouse Biol. 3:217-240 © 2013 by John Wiley & Sons, Inc.
Supporting Information
Filename | Description |
---|---|
cpmo130179-sup-0001-VideoS1.mp42.2 MB | Video 1 Liveimaging of a growing enteroid endogenously expressing RFP-tagged ZO1 (red) from day 3 to 6 under 2-D bright-field. Budding can be observed as the development of crypt-like domains that emanate from the sphere. Each frame is acquired in 30-min intervals. |
cpmo130179-sup-0002-VideoS2.wmv3.5 MB | Video 2 3-D reconstruction movie of an enteroid expressing RFP-tagged ZO1 (red).Budding can be observed as the development of crypt-like domains that emanate from the sphere. Each frame is acquired in 30-min intervals. |
cpmo130179-sup-0003-VideoS3.avi4.4 MB | Video 3 Bright-field and RFP-Tagged ZO1 (red) overlay during live imaging of a growing enteroid. Budding can be observed as the development of crypt-like domains that emanate from the sphere. Each frame is acquired in 30-min intervals. |
cpmo130179-sup-0004-VideoS4.mov15.7 MB | Video 4 3-D reconstruction of an enteroid crypt domain endogenously expressing ZO1-RFP (red) and immunostained for E-cadherin (green). |
cpmo130179-sup-0005-VideoS5.mov2.2 MB | Video 5 Liveimaging of a growing enteroid endogenously expressing cytosolic YFP from day 0 to 3 immediately after passaging. The enteroid moves in the Matrigel and budding occurs. The video shows 3-D YFP merged with bright-field and each frame is acquired in 20-min intervals. |
cpmo130179-sup-0006-VideoS6.mov3.2 MB | Video 6 Extrusion of dead cells (losing YFP) contained in the lumen to exterior.The video shows 3-D YFP merged with bright-field and each frame is acquired in 20-min intervals. |
cpmo130179-sup-0007-VideoS7.mov2.6 MB | Video 7 Stem cell containing crypt domain regenerates and seals to stay separated from damaged region made by passaging. The video shows 3-D YFP merged with bright-field and each frame is acquired in 20-min intervals. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Key References
- Barker et al., 2010. See above.
- Sato et al., 2009. See above.
- Sato et al., 2011. See above.
This paper describes, for the first time, the establishment of gastric epithelial organoids (gastroids).
The authors developed the conditions for a long-term culture of intestinal crypt-derived enteroids as well as the establishment of single Lgr5+ve+ve cell-derived enteroids. Methods described in this article are based on this paper.
In this study, colonic crypt-derived colonoids are generated based on the method developed by Sato et al. in 2009.