3D organoids derived from the small intestine: An emerging tool for drug transport research.
Acta Pharm Sin B
; 11(7): 1697-1707, 2021 Jul.
Article
em En
| MEDLINE
| ID: mdl-34386316
Small intestine in vitro models play a crucial role in drug transport research. Although conventional 2D cell culture models, such as Caco-2 monolayer, possess many advantages, they should be interpreted with caution because they have relatively poor physiologically reproducible phenotypes and functions. With the development of 3D culture technology, pluripotent stem cells (PSCs) and adult somatic stem cells (ASCs) show remarkable self-organization characteristics, which leads to the development of intestinal organoids. Based on previous studies, this paper reviews the application of intestinal 3D organoids in drug transport mediated by P-glycoprotein (P-gp), breast cancer resistance protein (BCRP) and multidrug resistance protein 2 (MRP2). The advantages and limitations of this model are also discussed. Although there are still many challenges, intestinal 3D organoid model has the potential to be an excellent tool for drug transport research.
3D organoid; ASCs, adult somatic stem cells; BCRP, breast cancer resistance protein; BMP, bone morphogenetic protein; CDF, 5(6)-carboxy-2',7'-dichlorofluorescein; Caco-2 cell monolayer; DDI, drugdrug interactions; Drug transporter; EGF, epidermal growth factor; ER, efflux ratio; ESCs, embryonic stem cells; FGF, fibroblast growth factor; Lgr5+, leucine-rich-repeat-containing G-protein-coupled receptor 5 positive; MCT, monocarboxylate transporter protein; MRP2, multidrug resistance protein 2; NBD, nucleotide-binding domain; OATP, organic anion transporting polypeptide; OCT, organic cation transporter; OCTN, carnitine/organic cation transporter; P-glycoprotein; P-gp, P-glycoprotein; PEPT, peptide transporter protein; PMAT, plasma membrane monoamine transporter; PSCs, pluripotent stem cells; Papp, apparent permeability coefficient; Rh123, rhodamine 123; SLC, solute carrier; Small intestine; TEER, transepithelial electrical resistance; TMDs, transmembrane domains; cMOAT, canalicular multispecific organic anion transporter; iPSCs, induced pluripotent stem cells
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Tipo de estudo:
Prognostic_studies
Idioma:
En
Revista:
Acta Pharm Sin B
Ano de publicação:
2021
Tipo de documento:
Article
País de afiliação:
China