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Permeability analyses and three dimensional imaging of interferon gamma-induced barrier disintegration in intestinal organoids

Authors :
Marco Bardenbacher
Barbara Ruder
Nathalie Britzen-Laurent
Benjamin Schmid
Maximilian Waldner
Elisabeth Naschberger
Michael Scharl
Werner Müller
Claudia Günther
Christoph Becker
Michael Stürzl
Philipp Tripal
Source :
Stem Cell Research, Vol 35, Iss , Pp - (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

The aberrant regulation of the epithelial barrier integrity is involved in many diseases of the digestive tract, including inflammatory bowel diseases and colorectal cancer. Intestinal epithelial cell organoid cultures provide new perspectives for analyses of the intestinal barrier in vitro. However, established methods of barrier function analyses from two dimensional cultures have to be adjusted to the analysis of three dimensional organoid structures. Here we describe the methodology for analysis of epithelial barrier function and molecular regulation in intestinal organoids. Barrier responses to interferon-γ of intestinal organoids with and without epithelial cell-specific deletion of the interferon-γ-receptor 2 gene were used as a model system. The established method allowed monitoring of the kinetics of interferon-γ-induced permeability changes in living organoids. Proteolytic degradation and altered localization of the tight junction proteins claudin-2, −7, and − 15 was detected using confocal spinning disc microscopy with 3D reconstruction. Hessian analysis was used for quantification of re-localization of claudins. In summary, we provide a novel methodologic approach for quantitative analyses of intestinal epithelial barrier functions in the 3D organoid model. Keywords: Inflammatory bowel disease, Interferon-gamma, Intestinal organoids, 3D imaging, Permeability, Tight junction

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
18735061
Volume :
35
Issue :
-
Database :
Directory of Open Access Journals
Journal :
Stem Cell Research
Publication Type :
Academic Journal
Accession number :
edsdoj.3f8738d9051e41d0b272e0b0f4ce94e7
Document Type :
article
Full Text :
https://doi.org/10.1016/j.scr.2019.101383