| Literature DB >> 30602618 |
Alessandro Donada1,2, Nathalie Balayn1, Dominika Sliwa1, Larissa Lordier1, Valentina Ceglia1, Francesco Baschieri1, Cyril Goizet3,4, Rémi Favier1,5, Lucie Tosca6, Gérard Tachdjian6, Cecile V Denis7, Isabelle Plo1, William Vainchenker1, Najet Debili1, Jean-Philippe Rosa7, Marijke Bryckaert7, Hana Raslova1.
Abstract
Filamin A (FLNa) links the cell membrane with the cytoskeleton and is central in several cellular processes. Heterozygous mutations in the X-linked FLNA gene are associated with a large spectrum of conditions, including macrothrombocytopenia, called filaminopathies. Using an isogenic pluripotent stem cell model derived from patients, we show that the absence of the FLNa protein in megakaryocytes (MKs) leads to their incomplete maturation, particularly the inability to produce proplatelets. Reduction in proplatelet formation potential is associated with a defect in actomyosin contractility, which results from inappropriate RhoA activation. This dysregulated RhoA activation was observed when MKs were plated on fibrinogen but not on other matrices (fibronectin, vitronectin, collagen 1, and von Willebrand factor), strongly suggesting a role for FLNa/αIIbβ3 interaction in the downregulation of RhoA activity. This was confirmed by experiments based on the overexpression of FLNa mutants deleted in the αIIbβ3-binding domain and the RhoA-interacting domain, respectively. Finally, pharmacological inhibition of the RhoA-associated kinase ROCK1/2 restored a normal phenotype and proplatelet formation. Overall, this work suggests a new etiology for macrothrombocytopenia, in which increased RhoA activity is associated with disrupted FLNa/αIIbβ3 interaction.Entities:
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Year: 2019 PMID: 30602618 PMCID: PMC6484462 DOI: 10.1182/blood-2018-07-861427
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113