Intestinal Stem Cell-on-Chip to Study Human Host-Microbiota Interaction

GND
1216425361
Zugehörigkeit
Center for Sepsis Control and Care & Institute of Biochemistry II, University Hospital Jena
Siwczak, Fatina;
Zugehörigkeit
Université de Nantes, Inserm, TENS, The Enteric Nervous System in Gut and Brain Diseases, IMAD
Loffet, Elise;
Zugehörigkeit
Center for Sepsis Control and Care & Institute of Biochemistry II, University Hospital Jena
Kaminska, Mathilda;
Zugehörigkeit
Center for Sepsis Control and Care & Institute of Biochemistry II, University Hospital Jena
Koceva, Hristina;
Zugehörigkeit
Université de Nantes, Inserm, TENS, The Enteric Nervous System in Gut and Brain Diseases, IMAD
Mahe, Maxime M.;
GND
1131810422
Zugehörigkeit
Center for Sepsis Control and Care & Institute of Biochemistry II, University Hospital Jena
Mosig, Alexander S.

The gut is a tubular organ responsible for nutrient absorption and harbors our intestinal microbiome. This organ is composed of a multitude of specialized cell types arranged in complex barrier-forming crypts and villi covered by a mucosal layer controlling nutrient passage and protecting from invading pathogens. The development and self-renewal of the intestinal epithelium are guided by niche signals controlling the differentiation of specific cell types along the crypt-villus axis in the epithelium. The emergence of microphysiological systems, or organ-on-chips, has paved the way to study the intestinal epithelium within a dynamic and controlled environment. In this review, we describe the use of organ-on-chip technology to control and guide these differentiation processes in vitro . We further discuss current applications and forthcoming strategies to investigate the mechanical processes of intestinal stem cell differentiation, tissue formation, and the interaction of the intestine with the microbiota in the context of gastrointestinal diseases.

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Rechteinhaber: Copyright © 2021 Siwczak, Loffet, Kaminska, Koceva, Mahe and Mosig

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Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.