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Cdc42‐dependent F‐actin dynamics drive structuration of the demarcation membrane system in megakaryocytes
Author(s) -
Antkowiak A.,
Viaud J.,
Severin S.,
Zanoun M.,
Ceccato L.,
Chicanne G.,
Strassel C.,
Eckly A.,
Leon C.,
Gachet C.,
Payrastre B.,
GaitsIacovoni F.
Publication year - 2016
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/jth.13318
Subject(s) - microbiology and biotechnology , cdc42 , actin cytoskeleton , cytoskeleton , actin , actin remodeling , biology , microtubule , biogenesis , chemistry , biochemistry , cell , gene
Essentials Information about the formation of the demarcation membrane system (DMS) is still lacking. We investigated the role of the cytoskeleton in DMS structuration in megakaryocytes. Cdc42/Pak‐dependent F‐actin remodeling regulates DMS organization for proper megakaryopoiesis. These data highlight the mandatory role of F‐actin in platelet biogenesis.Summary Background Blood platelet biogenesis results from the maturation of megakaryocytes ( MKs ), which involves the development of a complex demarcation membrane system ( DMS ). Therefore, MK differentiation is an attractive model for studying membrane remodeling. Objectives We sought to investigate the mechanism of DMS structuration in relationship to the cytoskeleton. Results Using three‐dimensional (3D) confocal imaging, we have identified consecutive stages of DMS organization that rely on F‐actin dynamics to polarize membranes and nuclei territories. Interestingly, microtubules are not involved in this process. We found that the mechanism underlying F‐actin‐dependent DMS formation required the activation of the guanosine triphosphate hydrolase Cdc42 and its p21‐activated kinase effectors (Pak1/2/3). Förster resonance energy transfer demonstrated that active Cdc42 was associated with endomembrane dynamics throughout terminal maturation. Inhibition of Cdc42 or Pak1/2/3 severely destructured the DMS and blocked proplatelet formation. Even though this process does not require containment within the hematopoietic niche, because DMS structuration was observed upon thrombopoietin‐treatment in suspension, integrin outside‐in signaling was required for Pak activation and probably resulted from secretion of extracellular matrix by MK s. Conclusions These data indicate a functional link, mandatory for MK differentiation, between actin dynamics, regulated by Cdc42/Pak1/2/3, and DMS maturation.