| Literature DB >> 26849305 |
Pengcheng Bu1, Lihua Wang2, Kai-Yuan Chen3, Tara Srinivasan4, Preetish Kadur Lakshminarasimha Murthy5, Kuei-Ling Tung2, Anastasia Kristine Varanko2, Huanhuan Joyce Chen6, Yiwei Ai3, Sarah King2, Steven M Lipkin7, Xiling Shen8.
Abstract
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.Entities:
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Year: 2016 PMID: 26849305 PMCID: PMC4751059 DOI: 10.1016/j.stem.2016.01.006
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633