miR-142 orchestrates a network of actin cytoskeleton regulators during megakaryopoiesis

Elife. 2014 May 23:3:e01964. doi: 10.7554/eLife.01964.

Abstract

Genome-encoded microRNAs (miRNAs) provide a posttranscriptional regulatory layer that controls the differentiation and function of various cellular systems, including hematopoietic cells. miR-142 is one of the most prevalently expressed miRNAs within the hematopoietic lineage. To address the in vivo functions of miR-142, we utilized a novel reporter and a loss-of-function mouse allele that we have recently generated. In this study, we show that miR-142 is broadly expressed in the adult hematopoietic system. Our data further reveal that miR-142 is critical for megakaryopoiesis. Genetic ablation of miR-142 caused impaired megakaryocyte maturation, inhibition of polyploidization, abnormal proplatelet formation, and thrombocytopenia. Finally, we characterized a network of miR-142-3p targets which collectively control actin filament homeostasis, thereby ensuring proper execution of actin-dependent proplatelet formation. Our study reveals a pivotal role for miR-142 activity in megakaryocyte maturation and function, and demonstrates a critical contribution of a single miRNA in orchestrating cytoskeletal dynamics and normal hemostasis.DOI: http://dx.doi.org/10.7554/eLife.01964.001.

Keywords: actin; cytoskeleton; megakaryocytes; megakaryopoiesis; miR-142; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism*
  • Animals
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Gene Expression Regulation
  • Genotype
  • HEK293 Cells
  • Hemostasis
  • Homeostasis
  • Humans
  • Megakaryocytes / metabolism*
  • Megakaryocytes / pathology
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Phenotype
  • RNA Interference
  • Signal Transduction
  • Thrombocytopenia / blood
  • Thrombocytopenia / genetics
  • Thrombocytopenia / metabolism*
  • Thrombopoiesis* / genetics
  • Transfection

Substances

  • Cytoskeletal Proteins
  • MicroRNAs
  • Mirn142 microRNA, mouse

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.