A miR-34a-Numb Feedforward Loop Triggered by Inflammation Regulates Asymmetric Stem Cell Division in Intestine and Colon Cancer

被引:128
作者
Bu, Pengcheng [1 ,2 ]
Wang, Lihua [3 ]
Chen, Kai-Yuan [1 ]
Srinivasan, Tara [2 ]
Murthy, Preetish Kadur Lakshminarasimha [4 ]
Tung, Kuei-Ling [3 ]
Varanko, Anastasia Kristine [3 ]
Chen, Huanhuan Joyce [5 ]
Ai, Yiwei [1 ]
King, Sarah [3 ]
Lipkin, Steven M. [6 ,7 ,8 ]
Shen, Xiling [1 ,2 ,3 ,9 ]
机构
[1] Cornell Univ, Sch Elect & Comp Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[3] Cornell Univ, Dept Biol & Environm Engn, Ithaca, NY 14853 USA
[4] Cornell Univ, Sch Mech Aerosp Engn, Ithaca, NY 14853 USA
[5] Weill Cornell Med Coll, Meyer Canc Ctr, New York, NY 10021 USA
[6] Weill Cornell Med Coll, Dept Med, New York, NY 10021 USA
[7] Weill Cornell Med Coll, Dept Med Genet, New York, NY 10021 USA
[8] Weill Cornell Med Coll, Dept Surg, New York, NY 10021 USA
[9] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
基金
美国国家科学基金会;
关键词
BOWEL-DISEASE; NOTCH; ROBUSTNESS; GENE; DIFFERENTIATION; MICRORNAS; PROTEINS; BARRIER; PROVIDE; SYSTEM;
D O I
10.1016/j.stem.2016.01.006
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Emerging evidence suggests that microRNAs can initiate asymmetric division, but whether microRNA and protein cell fate determinants coordinate with each other remains unclear. Here, we show that miR-34a directly suppresses Numb in early-stage colon cancer stem cells (CCSCs), forming an incoherent feedforward loop (IFFL) targeting Notch to separate stem and non-stem cell fates robustly. Perturbation of the IFFL leads to a new intermediate cell population with plastic and ambiguous identity. Lgr5+ mouse intestinal/colon stem cells (ISCs) predominantly undergo symmetric division but turn on asymmetric division to curb the number of ISCs when proinflammatory response causes excessive proliferation. Deletion of miR-34a inhibits asymmetric division and exacerbates Lgr5+ ISC proliferation under such stress. Collectively, our data indicate that microRNA and protein cell fate determinants coordinate to enhance robustness of cell fate decision, and they provide a safeguard mechanism against stem cell proliferation induced by inflammation or oncogenic mutation.
引用
收藏
页码:189 / 202
页数:14
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