TY - JOUR
T1 - Three-Dimensional Gastrointestinal Organoid Culture in Combination with Nerves or Fibroblasts
T2 - A Method to Characterize the Gastrointestinal Stem Cell Niche
AU - Pastuła, Agnieszka
AU - Middelhoff, Moritz
AU - Brandtner, Anna
AU - Tobiasch, Moritz
AU - Höhl, Bettina
AU - Nuber, Andreas H.
AU - Demir, Ihsan Ekin
AU - Neupert, Steffi
AU - Kollmann, Patrick
AU - Mazzuoli-Weber, Gemma
AU - Quante, Michael
N1 - Publisher Copyright:
© 2016 Agnieszka Pastuła et al.
PY - 2016
Y1 - 2016
N2 - The gastrointestinal epithelium is characterized by a high turnover of cells and intestinal stem cells predominantly reside at the bottom of crypts and their progeny serve to maintain normal intestinal homeostasis. Accumulating evidence demonstrates the pivotal role of a niche surrounding intestinal stem cells in crypts, which consists of cellular and soluble components and creates an environment constantly influencing the fate of stem cells. Here we describe different 3D culture systems to culture gastrointestinal epithelium that should enable us to study the stem cell niche in vitro in the future: organoid culture and multilayered systems such as organotypic cell culture and culture of intestinal tissue fragments ex vivo. These methods mimic the in vivo situation in vitro by creating 3D culture conditions that reflect the physiological situation of intestinal crypts. Modifications of the composition of the culture media as well as coculturing epithelial organoids with previously described cellular components such as myofibroblasts, collagen, and neurons show the impact of the methods applied to investigate niche interactions in vitro. We further present a novel method to isolate labeled nerves from the enteric nervous system using Dclk1-CreGFP mice.
AB - The gastrointestinal epithelium is characterized by a high turnover of cells and intestinal stem cells predominantly reside at the bottom of crypts and their progeny serve to maintain normal intestinal homeostasis. Accumulating evidence demonstrates the pivotal role of a niche surrounding intestinal stem cells in crypts, which consists of cellular and soluble components and creates an environment constantly influencing the fate of stem cells. Here we describe different 3D culture systems to culture gastrointestinal epithelium that should enable us to study the stem cell niche in vitro in the future: organoid culture and multilayered systems such as organotypic cell culture and culture of intestinal tissue fragments ex vivo. These methods mimic the in vivo situation in vitro by creating 3D culture conditions that reflect the physiological situation of intestinal crypts. Modifications of the composition of the culture media as well as coculturing epithelial organoids with previously described cellular components such as myofibroblasts, collagen, and neurons show the impact of the methods applied to investigate niche interactions in vitro. We further present a novel method to isolate labeled nerves from the enteric nervous system using Dclk1-CreGFP mice.
UR - http://www.scopus.com/inward/record.url?scp=84949958627&partnerID=8YFLogxK
U2 - 10.1155/2016/3710836
DO - 10.1155/2016/3710836
M3 - Article
AN - SCOPUS:84949958627
SN - 1687-9678
VL - 2016
JO - Stem Cells International
JF - Stem Cells International
M1 - 3710836
ER -