Sangiorgi Eugenio, Capecchi Mario R
Howard Hughes Medical Institute and Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Nat Genet. 2008 Jul;40(7):915-20. doi: 10.1038/ng.165. Epub 2008 Jun 8.
Bmi1 plays an essential part in the self-renewal of hematopoietic and neural stem cells. To investigate its role in other adult stem cell populations, we generated a mouse expressing a tamoxifen-inducible Cre from the Bmi1 locus. We found that Bmi1 is expressed in discrete cells located near the bottom of crypts in the small intestine, predominantly four cells above the base of the crypt (+4 position). Over time, these cells proliferate, expand, self-renew and give rise to all the differentiated cell lineages of the small intestine epithelium. The induction of a stable form of beta-catenin in these cells was sufficient to rapidly generate adenomas. Moreover, ablation of Bmi1(+) cells using a Rosa26 conditional allele, expressing diphtheria toxin, led to crypt loss. These experiments identify Bmi1 as an intestinal stem cell marker in vivo. Unexpectedly, the distribution of Bmi1-expressing stem cells along the length of the small intestine suggested that mammals use more than one molecularly distinguishable adult stem cell subpopulation to maintain organ homeostasis.
Bmi1在造血干细胞和神经干细胞的自我更新中起着至关重要的作用。为了研究其在其他成体干细胞群体中的作用,我们构建了一种在Bmi1基因座表达他莫昔芬诱导型Cre的小鼠。我们发现Bmi1在位于小肠隐窝底部附近的离散细胞中表达,主要在隐窝底部上方四个细胞处(+4位置)。随着时间的推移,这些细胞增殖、扩增、自我更新,并产生小肠上皮的所有分化细胞谱系。在这些细胞中诱导稳定形式的β-连环蛋白足以快速产生腺瘤。此外,使用表达白喉毒素的Rosa26条件等位基因消融Bmi1(+)细胞会导致隐窝丢失。这些实验确定Bmi1为体内小肠干细胞标志物。出乎意料的是,表达Bmi1的干细胞沿小肠长度的分布表明,哺乳动物使用不止一种分子可区分的成体干细胞亚群来维持器官稳态。