4.7 Article

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

Journal

CELL STEM CELL
Volume 18, Issue 2, Pages 189-202

Publisher

CELL PRESS
DOI: 10.1016/j.stem.2016.01.006

Keywords

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Funding

  1. NIH [R01GM95990, R01GM114254]
  2. NSF [1350659, 1137269]
  3. NYSTEM [C029543]
  4. DARPA [19-1091726]
  5. Directorate For Engineering
  6. Emerging Frontiers & Multidisciplinary Activities [1137269] Funding Source: National Science Foundation
  7. Div Of Chem, Bioeng, Env, & Transp Sys
  8. Directorate For Engineering [1350659] Funding Source: National Science Foundation

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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.

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