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鼠端粒酶逆转录酶(mTert)表达标志着缓慢循环的肠道干细胞。

Mouse telomerase reverse transcriptase (mTert) expression marks slowly cycling intestinal stem cells.

机构信息

Division of Gastroenterology, Children's Hospital Boston, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):179-84. doi: 10.1073/pnas.1013004108. Epub 2010 Dec 20.

Abstract

The intestinal epithelium is maintained by a population of rapidly cycling (Lgr5(+)) intestinal stem cells (ISCs). It has been postulated, however, that slowly cycling ISCs must also be present in the intestine to protect the genome from accumulating deleterious mutations and to allow for a response to tissue injury. Here, we identify a subpopulation of slowly cycling ISCs marked by mouse telomerase reverse transcriptase (mTert) expression that can give rise to Lgr5(+) cells. mTert-expressing cells distribute in a pattern along the crypt-villus axis similar to long-term label-retaining cells (LRCs) and are resistant to tissue injury. Lineage-tracing studies demonstrate that mTert(+) cells give rise to all differentiated intestinal cell types, persist long term, and contribute to the regenerative response following injury. Consistent with other highly regenerative tissues, our results demonstrate that a slowly cycling stem cell population exists within the intestine.

摘要

肠上皮由一群快速循环(Lgr5(+))肠干细胞(ISCs)维持。然而,有人推测,缓慢循环的 ISC 也必须存在于肠道中,以防止基因组积累有害突变,并对组织损伤做出反应。在这里,我们鉴定出一个由小鼠端粒酶逆转录酶(mTert)表达标记的缓慢循环 ISC 亚群,它可以产生 Lgr5(+)细胞。mTert 表达细胞沿隐窝-绒毛轴呈分布模式,类似于长期标记保留细胞(LRCs),并且对组织损伤具有抗性。谱系追踪研究表明,mTert(+)细胞产生所有分化的肠细胞类型,长期存在,并有助于损伤后的再生反应。与其他高度再生组织一致,我们的结果表明,肠道内存在一个缓慢循环的干细胞群体。

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