Abstract
The study of gene function in endodermal epithelia such as of stomach, small intestine and colon relies heavily on transgenic approaches. Establishing such animal models is laborious, expensive and time-consuming. We present here a method based on Cre recombinase-inducible retrovirus vectors that allows the conditional manipulation of gene expression in primary mouse organoid culture systems.
MeSH Terms
Animals
Gene Expression
Gene Knockdown Techniques/methods
Green Fluorescent Proteins/genetics
Humans
Integrases/metabolism
Intestinal Mucosa/cytology
Mice
Organoids/cytology,metabolism
Receptors, G-Protein-Coupled/physiology
Receptors, Notch/physiology
Retroviridae/genetics
Stem Cells/virology
Tamoxifen/analogs & derivatives,pharmacology
Transduction, Genetic/methods
Chemicals
Lgr5 protein, mouse
Receptors, G-Protein-Coupled
Receptors, Notch
enhanced green fluorescent protein
Tamoxifen
Green Fluorescent Proteins
afimoxifene
Cre recombinase
Integrases
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Koo Bon-Kyoung
Hubrecht Institute for Developmental Biology and Stem Cell Research, and University Medical Centre, Utrecht, The Netherlands.
Stange Daniel E
Sato Toshiro
Karthaus Wouter
Farin Henner F
Huch Meritxell
van Es Johan H
Clevers Hans
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