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

Cell Stem Cell. 2016 Feb 4;18(2):189-202. doi: 10.1016/j.stem.2016.01.006.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Asymmetric Cell Division* / drug effects
  • Base Sequence
  • Cell Differentiation / drug effects
  • Cell Lineage / drug effects
  • Cell Proliferation / drug effects
  • Gene Knockdown Techniques
  • Inflammation / pathology*
  • Membrane Proteins / metabolism*
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Molecular Sequence Data
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology*
  • Nerve Tissue Proteins / metabolism*
  • Receptors, Notch / metabolism
  • Stress, Physiological / drug effects
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • MIRN34a microRNA, mouse
  • Membrane Proteins
  • MicroRNAs
  • Nerve Tissue Proteins
  • Numb protein, mouse
  • Receptors, Notch
  • Tumor Necrosis Factor-alpha