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

被引:417
作者
Montgomery, Robert K. [1 ,4 ]
Carlone, Diana L. [2 ,4 ]
Richmond, Camilla A. [1 ,2 ,4 ]
Farilla, Loredana [2 ,4 ]
Kranendonk, Mariette E. G. [2 ]
Henderson, Daniel E. [2 ]
Baffour-Awuah, Nana Yaa [1 ]
Ambruzs, Dana M. [2 ]
Fogli, Laura K. [2 ]
Algra, Selma [1 ]
Breault, David T. [2 ,3 ,4 ]
机构
[1] Childrens Hosp Boston, Div Gastroenterol, Boston, MA 02115 USA
[2] Childrens Hosp Boston, Div Endocrinol, Boston, MA 02115 USA
[3] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[4] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
关键词
HAIR FOLLICLE; TISSUES; BIOLOGY; CANCER; CRYPT; SKIN; IDENTIFICATION; PROLIFERATION; RADIATION; MODEL;
D O I
10.1073/pnas.1013004108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:179 / 184
页数:6
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