TY - CHAP
T1 - Primary mouse small intestinal epithelial cell cultures
AU - Sato, Toshiro
AU - Clevers, Hans
PY - 2013
Y1 - 2013
N2 - The intestinal epithelium is the most rapidly self-renewing tissue in adult mammals. We have recently shown that Lgr5 (Leucine-rich repeat-containing G protein-coupled receptor) is expressed in intestinal stem cells by an in vivo genetic lineage tracing strategy. In the past, extensive efforts have been made to establish primary small intestinal culture systems. However, no defined, reproducible and robust culture system had been developed. To establish such a system, we screened for optimal growth factor combinations based on genetic evidence of self-renewal regulation, differentiation, and carcinogenesis of intestinal stem cells. Here, we describe methods that we have established for the isolation and culture of primary small intestinal epithelial stem cells. In this culture system, isolated crypts form organoid structures with a histological hierarchy recapitulating in vivo small intestinal epithelium. Single isolated Lgr5+ intestinal stem cells also form these organoid structures, in which stem cells are maintained by self-renewal and give rise to all lineages of the intestinal epithelium. This culture system is particularly useful for studying the regulation of intestinal stem cell self-renewal and differentiation.
AB - The intestinal epithelium is the most rapidly self-renewing tissue in adult mammals. We have recently shown that Lgr5 (Leucine-rich repeat-containing G protein-coupled receptor) is expressed in intestinal stem cells by an in vivo genetic lineage tracing strategy. In the past, extensive efforts have been made to establish primary small intestinal culture systems. However, no defined, reproducible and robust culture system had been developed. To establish such a system, we screened for optimal growth factor combinations based on genetic evidence of self-renewal regulation, differentiation, and carcinogenesis of intestinal stem cells. Here, we describe methods that we have established for the isolation and culture of primary small intestinal epithelial stem cells. In this culture system, isolated crypts form organoid structures with a histological hierarchy recapitulating in vivo small intestinal epithelium. Single isolated Lgr5+ intestinal stem cells also form these organoid structures, in which stem cells are maintained by self-renewal and give rise to all lineages of the intestinal epithelium. This culture system is particularly useful for studying the regulation of intestinal stem cell self-renewal and differentiation.
KW - Confocal immunofluorescence
KW - Flow cytometry
KW - Intestinal stem cells
KW - Lgr5
KW - Small intestinal crypts
KW - Wnt signal
UR - http://www.scopus.com/inward/record.url?scp=84870489063&partnerID=8YFLogxK
U2 - 10.1007/978-1-62703-125-7_19
DO - 10.1007/978-1-62703-125-7_19
M3 - Chapter
C2 - 23097115
AN - SCOPUS:84870489063
SN - 9781627031240
T3 - Methods in Molecular Biology
SP - 319
EP - 328
BT - Epithelial Cell Culture Protocols
A2 - Randell, Scott
A2 - Fulcher, Leslie
ER -