Volume 3, Issue 4 p. 217-240

Establishment of Gastrointestinal Epithelial Organoids

Maxime M. Mahe

Maxime M. Mahe

Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio

These authors contributed equally to this work

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Eitaro Aihara

Eitaro Aihara

Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio

These authors contributed equally to this work

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Michael A. Schumacher

Michael A. Schumacher

Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio

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Yana Zavros

Yana Zavros

Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio

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Marshall H. Montrose

Marshall H. Montrose

Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio

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Michael A. Helmrath

Michael A. Helmrath

Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio

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Toshiro Sato

Toshiro Sato

Department of Gastroenterology, School of Medicine, Keio University, Tokyo, Japan

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Noah F. Shroyer

Noah F. Shroyer

Division of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Research Center, Cincinnati, Ohio

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First published: 19 December 2013
Citations: 227

Abstract

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.

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