LGR5型
生物
Wnt信号通路
细胞生物学
干细胞
肠上皮
丹麦克朗
Notch信号通路
癌症研究
上皮
细胞分化
免疫学
信号转导
遗传学
基因
作者
Akifumi Ootani,Xingnan Li,Eugenio Sangiorgi,Q Ho,Hiroo Ueno,Shuji Toda,Hajime Sugihara,Kazuma Fujimoto,Irving L. Weissman,Mario R. Capecchi,Calvin J. Kuo
出处
期刊:Nature Medicine
[Springer Nature]
日期:2009-04-27
卷期号:15 (6): 701-706
被引量:809
摘要
The development of a long-term intestinal culture system has, until recently, eluded researchers. Here the authors describe a method allowing long-term culture of both small intestine and colon that incorporates an air-liquid interface coupled with a three-dimensional matrix scaffold. The cultures show epithelial cell proliferation and multilineage differentiation to the major cell types and accurately recapitulate the Wnt- and Notch-dependent intestinal stem cell niche. The in vitro analysis of intestinal epithelium has been hampered by a lack of suitable culture systems. Here we describe robust long-term methodology for small and large intestinal culture, incorporating an air-liquid interface and underlying stromal elements. These cultures showed prolonged intestinal epithelial expansion as sphere-like organoids with proliferation and multilineage differentiation. The Wnt growth factor family positively regulates proliferation of the intestinal epithelium in vivo. Accordingly, culture growth was inhibited by the Wnt antagonist Dickkopf-1 (Dkk1) and markedly stimulated by a fusion protein between the Wnt agonist R-spondin-1 and immunoglobulin Fc (RSpo1-Fc). Furthermore, treatment with the γ-secretase inhibitor dibenzazepine and neurogenin-3 overexpression induced goblet cell and enteroendocrine cell differentiation, respectively, consistent with endogenous Notch signaling and lineage plasticity. Epithelial cells derived from both leucine-rich repeat-containing G protein–coupled receptor-5–positive (Lgr5+) and B lymphoma moloney murine leukemia virus insertion region homolog-1–positive (Bmi1+) lineages, representing putative intestinal stem cell (ISC) populations, were present in vitro and were expanded by treatment with RSpo1-Fc; this increased number of Lgr5+ cells upon RSpo1-Fc treatment was subsequently confirmed in vivo. Our results indicate successful long-term intestinal culture within a microenvironment accurately recapitulating the Wnt- and Notch-dependent ISC niche.
科研通智能强力驱动
Strongly Powered by AbleSci AI