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Lgr5 表达的主细胞驱动胃泌酸区的上皮再生和癌症。

Lgr5-expressing chief cells drive epithelial regeneration and cancer in the oxyntic stomach.

机构信息

A*STAR Institute of Medical Biology, 138648, Singapore.

Cancer Research Institute, Kanazawa University, Kakuma-machi Kanazawa 920-1192, Japan.

出版信息

Nat Cell Biol. 2017 Jul;19(7):774-786. doi: 10.1038/ncb3541. Epub 2017 Jun 5.

Abstract

The daily renewal of the corpus epithelium is fuelled by adult stem cells residing within tubular glands, but the identity of these stem cells remains controversial. Lgr5 marks homeostatic stem cells and 'reserve' stem cells in multiple tissues. Here, we report Lgr5 expression in a subpopulation of chief cells in mouse and human corpus glands. Using a non-variegated Lgr5-2A-CreERT2 mouse model, we show by lineage tracing that Lgr5-expressing chief cells do not behave as corpus stem cells during homeostasis, but are recruited to function as stem cells to effect epithelial renewal following injury by activating Wnt signalling. Ablation of Lgr5 cells severely impairs epithelial homeostasis in the corpus, indicating an essential role for these Lgr5 cells in maintaining the homeostatic stem cell pool. We additionally define Lgr5 chief cells as a major cell-of-origin of gastric cancer. These findings reveal clinically relevant insights into homeostasis, repair and cancer in the corpus.

摘要

腺胃上皮的日常更新由位于管状腺内的成体干细胞所驱动,但这些干细胞的身份仍存在争议。Lgr5 标记着多种组织中的稳态干细胞和“储备”干细胞。在这里,我们报告了在小鼠和人类腺胃中的主细胞亚群中表达 Lgr5。使用非镶嵌 Lgr5-2A-CreERT2 小鼠模型,我们通过谱系追踪表明,在稳态下,表达 Lgr5 的主细胞不作为腺胃干细胞发挥作用,而是在受到损伤后通过激活 Wnt 信号被招募来作为干细胞发挥作用,以促进上皮更新。Lgr5 细胞的缺失严重损害了腺胃的上皮稳态,表明这些 Lgr5 细胞对于维持稳态干细胞池具有重要作用。我们还将 Lgr5 主细胞定义为胃癌的主要起始细胞。这些发现揭示了腺胃中稳态、修复和癌症的临床相关见解。

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