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Lgr5(+) 干细胞驱动胃的自我更新,并在体外构建长寿的胃单位。

Lgr5(+ve) stem cells drive self-renewal in the stomach and build long-lived gastric units in vitro.

机构信息

Hubrecht Institute for Developmental Biology and Stem Cell Research, Uppsalalaan 8, 3584CT Utrecht & University Medical Centre Utrecht, Netherlands.

出版信息

Cell Stem Cell. 2010 Jan 8;6(1):25-36. doi: 10.1016/j.stem.2009.11.013.

Abstract

The study of gastric epithelial homeostasis and cancer has been hampered by the lack of stem cell markers and in vitro culture methods. The Wnt target gene Lgr5 marks stem cells in the small intestine, colon, and hair follicle. Here, we investigated Lgr5 expression in the stomach and assessed the stem cell potential of the Lgr5(+ve) cells by using in vivo lineage tracing. In neonatal stomach, Lgr5 was expressed at the base of prospective corpus and pyloric glands, whereas expression in the adult was predominantly restricted to the base of mature pyloric glands. Lineage tracing revealed these Lgr5(+ve) cells to be self-renewing, multipotent stem cells responsible for the long-term renewal of the gastric epithelium. With an in vitro culture system, single Lgr5(+ve) cells efficiently generated long-lived organoids resembling mature pyloric epithelium. The Lgr5 stem cell marker and culture method described here will be invaluable tools for accelerating research into gastric epithelial renewal, inflammation/infection, and cancer.

摘要

胃上皮细胞稳态和癌症的研究一直受到缺乏干细胞标志物和体外培养方法的阻碍。Wnt 靶基因 Lgr5 标记小肠、结肠和毛囊中的干细胞。在这里,我们研究了胃中的 Lgr5 表达,并通过体内谱系追踪评估了 Lgr5(+ve)细胞的干细胞潜能。在新生胃中,Lgr5 在未来的胃体和幽门腺的底部表达,而在成年胃中,Lgr5 的表达主要局限于成熟幽门腺的底部。谱系追踪显示这些 Lgr5(+ve)细胞是自我更新的多能干细胞,负责胃上皮的长期更新。通过体外培养系统,单个 Lgr5(+ve)细胞有效地生成类似于成熟幽门上皮的长期存在的类器官。这里描述的 Lgr5 干细胞标志物和培养方法将是加速胃上皮细胞更新、炎症/感染和癌症研究的宝贵工具。

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