TY - JOUR
T1 - MiR-142 orchestrates a network of actin cytoskeleton regulators during megakaryopoiesis
AU - Chapnik, Elik
AU - Rivkin, Natalia
AU - Mildner, Alexander
AU - Beck, Gilad
AU - Pasvolsky, Ronit
AU - Metzl-Raz, Eyal
AU - Birger, Yehudit
AU - Amir, Gail
AU - Tirosh, Itay
AU - Porat, Ziv
AU - Lellouche, Emmanuel
AU - Michaeli, Shulamit
AU - Lellouche, Jean-paul M.
AU - Izraeli, Shai
AU - Jung, Steffen
AU - Hornstein, Eran
AU - Israel, Liron
PY - 2014/5/23
Y1 - 2014/5/23
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84902307914&partnerID=8YFLogxK
U2 - https://doi.org/10.7554/eLife.01964
DO - https://doi.org/10.7554/eLife.01964
M3 - مقالة
C2 - 24859754
SN - 2050-084X
VL - 2014
JO - eLife
JF - eLife
IS - 3
M1 - e01964
ER -