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

  • Elik Chapnik
  • , Natalia Rivkin
  • , Alexander Mildner
  • , Gilad Beck
  • , Ronit Pasvolsky
  • , Eyal Metzl-Raz
  • , Yehudit Birger
  • , Gail Amir
  • , Itay Tirosh
  • , Ziv Porat
  • , Liron Israel
  • , Emmanuel Lellouche
  • , Shulamit Michaeli
  • , Jean Paul Lellouche
  • , Shai Izraeli
  • , Steffen Jung
  • , Eran Hornstein

Research output: Contribution to journalArticlepeer-review

75 Scopus citations

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 loss-of-function mouse allele that we have recently generated. Here, we show that miR-142 is broadly expressed in the adult hematopoietic system. Our data further reveal that miR-142 is critical for megakaryopoiesis. Thus, genetic miR-142 ablation caused impaired megakaryocyte maturation, inhibition of polyploidization, abnormal proplatelet formation, and thrombocytopenia. Finally, we characterize a network of miR-142-3p targets which collectively controls 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 haemostasis.

Original languageEnglish
Article numbere01964
JournaleLife
Volume2014
Issue number3
DOIs
StatePublished - 23 May 2014

Fingerprint

Dive into the research topics of 'MiR-142 orchestrates a network of actin cytoskeleton regulators during megakaryopoiesis'. Together they form a unique fingerprint.

Cite this