Identification of Quiescent LGR5
Intestinal Stem Cell
Organoids
Slow-Cycling Stem Cell
TGF-β Signaling
Journal
Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
received:
13
10
2021
revised:
16
07
2022
accepted:
19
07
2022
pubmed:
14
8
2022
medline:
26
10
2022
entrez:
13
8
2022
Statut:
ppublish
Résumé
In the mouse intestinal epithelium, Lgr5 Transcriptional heterogeneity among colonic epithelial cells was analyzed by means of single-cell RNA sequencing analysis of human and mouse colonic epithelial cells. To trace the fate of human colonic stem or differentiated cells, we generated LGR5-tdTomato, LGR5-iCasase9-tdTomato, LGR5-split-Cre, and KRT20-ERCreER knock-in human colon organoids via genome engineering. p27 Single-cell RNA sequencing analysis illuminated the presence of nondividing LGR5 Our results highlight the quiescent nature of human LGR5
Sections du résumé
BACKGROUND & AIMS
In the mouse intestinal epithelium, Lgr5
METHODS
Transcriptional heterogeneity among colonic epithelial cells was analyzed by means of single-cell RNA sequencing analysis of human and mouse colonic epithelial cells. To trace the fate of human colonic stem or differentiated cells, we generated LGR5-tdTomato, LGR5-iCasase9-tdTomato, LGR5-split-Cre, and KRT20-ERCreER knock-in human colon organoids via genome engineering. p27
RESULTS
Single-cell RNA sequencing analysis illuminated the presence of nondividing LGR5
CONCLUSIONS
Our results highlight the quiescent nature of human LGR5
Identifiants
pubmed: 35963362
pii: S0016-5085(22)00912-X
doi: 10.1053/j.gastro.2022.07.081
pii:
doi:
Substances chimiques
Receptors, G-Protein-Coupled
0
Fluorouracil
U3P01618RT
Transforming Growth Factors
76057-06-2
LGR5 protein, human
0
Lgr5 protein, mouse
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1391-1406.e24Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.