MicroRNA-449a levels increase by several orders of magnitude during mucociliary differentiation of airway epithelia

Cell Cycle. 2010 Nov 15;9(22):4579-83. doi: 10.4161/cc.9.22.13870. Epub 2010 Nov 15.

Abstract

MicroRNAs of the miR-34/449 family mediate cell cycle arrest and tumor suppression. Here we show that the expression of microRNA miR-449a, unlike its paralogue miR-34a, is highly tissue specific and largely restricted to pulmonary and testicular tissue. MiR-449a levels in the murine lung are particularly high shortly before and after birth, coinciding with terminal differentiation of lung epithelia. Strikingly, miR-449a is upregulated by more than 1000-fold when epithelial cells from human airways are lifted from a liquid environment to air, allowing them to undergo mucociliary differentiation. The induction of miR-449a occurs in parallel to its host gene CDC20B and the transcription factor FoxJ1. Exposure to tobacco smoke induces a moderate further increase in the levels of miR-449a, and also miR-34a, in differentiated airway epithelia. We propose that miR-449a can serve as an exquisitely sensitive and specific biomarker for the differentiation of bronchial epithelia. Moreover, miR-449a may actively promote mucociliary differentiation through its ability to block cell cycle progression, and it may conribute to a first line of defence against genotoxic stress by its proapoptotic functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cdc20 Proteins
  • Cell Cycle Proteins / metabolism
  • Cell Differentiation
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism*
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Lung / metabolism
  • Mice
  • MicroRNAs / metabolism*
  • Respiratory Mucosa / cytology
  • Respiratory Mucosa / metabolism*
  • Smoking

Substances

  • Cdc20 Proteins
  • Cdc20 protein, mouse
  • Cell Cycle Proteins
  • FOXJ1 protein, mouse
  • Forkhead Transcription Factors
  • MicroRNAs
  • Mirn449 microRNA, mouse