Freeman Hugh-James
Department of Medicine-Gastroenterology, University of British Columbia Hospital, 2211 Wesbrook Mall, Vancouver V6T 1W5, Canada.
World J Gastroenterol. 2008 Dec 21;14(47):7160-2. doi: 10.3748/wjg.14.7160.
The intestinal epithelial lining plays a central role in the digestion and absorption of nutrients, but exists in a harsh luminal environment that necessitates continual renewal. This renewal process involves epithelial cell proliferation in the crypt base and later cell migration from the crypt base to the luminal surface. This process is dependent on multi-potent progenitor cells, or stem cells, located in each crypt. There are about 4 to 6 stem cells per crypt, and these stem cells are believed to generate distinct end-differentiated epithelial cell types, including absorptive cells, goblet cells, enteroendocrine cells and Paneth cells, while also maintaining their own progenitor cell state. Earlier studies suggested that intestinal stem cells were located either in the crypt base interspersed between the Paneth cells [i.e. crypt base columnar (CBC) cell model] or at an average position of 4 cells from the crypt base [i.e. label-retaining cells (LRC +4) model]. Recent studies have employed biomarkers in the in vivo mammalian state to more precisely evaluate the location of these progenitor cells in the intestinal crypt. Most notable of these novel markers are Lgr5, a gene that encodes a G-protein-coupled receptor with expression restricted to CBC cells, and Bmi 1, which encodes a chromatin remodeling protein expressed by LRC. These studies raise the possibility that there may be separate stem cell lines or different states of stem cell activation involved in the renewal of normal mammalian intestinal tract.
肠道上皮内衬在营养物质的消化和吸收中起核心作用,但存在于恶劣的管腔环境中,这就需要不断更新。这个更新过程涉及隐窝底部的上皮细胞增殖,以及随后细胞从隐窝底部向管腔表面的迁移。这个过程依赖于位于每个隐窝中的多能祖细胞或干细胞。每个隐窝大约有4到6个干细胞,这些干细胞被认为可以产生不同的终末分化上皮细胞类型,包括吸收细胞、杯状细胞、肠内分泌细胞和潘氏细胞,同时还能维持自身的祖细胞状态。早期研究表明,肠道干细胞要么位于潘氏细胞之间的隐窝底部(即隐窝基底柱状细胞模型),要么位于距隐窝底部平均4个细胞的位置(即标记保留细胞模型)。最近的研究在体内哺乳动物状态下使用生物标志物,以更精确地评估这些祖细胞在肠道隐窝中的位置。这些新型标志物中最值得注意的是Lgr5,一种编码G蛋白偶联受体的基因,其表达仅限于隐窝基底柱状细胞,以及Bmi 1,它编码一种由标记保留细胞表达的染色质重塑蛋白。这些研究提出了一种可能性,即在正常哺乳动物肠道更新过程中可能存在不同的干细胞系或不同的干细胞激活状态。