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Chemically-defined and scalable culture system for intestinal stem cells derived from human intestinal organoids.

Authors :
Kwon O
Lee H
Jung J
Son YS
Jeon S
Yoo WD
Son N
Jung KB
Choi E
Lee IC
Kwon HJ
Kim C
Lee MO
Cho HS
Kim DS
Son MY
Source :
Nature communications [Nat Commun] 2024 Jan 27; Vol. 15 (1), pp. 799. Date of Electronic Publication: 2024 Jan 27.
Publication Year :
2024

Abstract

Three-dimensional human intestinal organoids (hIO) are widely used as a platform for biological and biomedical research. However, reproducibility and challenges for large-scale expansion limit their applicability. Here, we establish a human intestinal stem cell (ISC) culture method expanded under feeder-free and fully defined conditions through selective enrichment of ISC populations (ISC <superscript>3D-hIO</superscript> ) within hIO derived from human pluripotent stem cells. The intrinsic self-organisation property of ISC <superscript>3D-hIO</superscript> , combined with air-liquid interface culture in a minimally defined medium, forces ISC <superscript>3D-hIO</superscript> to differentiate into the intestinal epithelium with cellular diversity, villus-like structure, and barrier integrity. Notably, ISC <superscript>3D-hIO</superscript> is an ideal cell source for gene editing to study ISC biology and transplantation for intestinal diseases. We demonstrate the intestinal epithelium differentiated from ISC <superscript>3D-hIO</superscript> as a model system to study severe acute respiratory syndrome coronavirus 2 viral infection. ISC <superscript>3D-hIO</superscript> culture technology provides a biological tool for use in regenerative medicine and disease modelling.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
38280855
Full Text :
https://doi.org/10.1038/s41467-024-45103-7