Cells · 2021 · 21 citations · 25 references
Life SciencesCell BiologyMolecular BiologyIon Channel BiophysicsMolecular PharmacologyTissue EngineeringCystic FibrosisEpithelial Barrier FunctionIntestinal Barrier FunctionCftr Gene MutationsCftr Protein FunctionChannelsDifferentiation In Epithelial OrganoidsElectrogenic TransportEpithelial Water TransportFluorescence-based AssaysOrganoids
Induced Pluripotent Stem Cells (iPSCs) can be differentiated into epithelial organoids that recapitulate the relevant context for CFTR and enable testing of therapies targeting Cystic Fibrosis (CF)-causing mutant proteins. However, to date, CF-iPSC-derived organoids have only been used to study pharmacological modulation of mutant CFTR channel activity and not the activity of other disease-relevant membrane protein constituents. In the current work, we describe a high-throughput, fluorescence-based assay of CFTR channel activity in iPSC-derived intestinal organoids and describe how this method can be adapted to study other apical membrane proteins. Specifically, we show how this assay can be employed to study CFTR and ENaC channels and an electrogenic acid transporter in the same iPSC-derived intestinal tissue. This phenotypic platform promises to expand CF therapy discovery to include strategies that target multiple determinants of epithelial fluid transport.
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An in vivo model of human small intestine using pluripotent stem cells
Carey L. Watson, Maxime M. Mahé, Jorge O. Múnera et al. · Nature Medicine · 2014 · 577 citations