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Published on: November 11, 2018
Role of Rho-GTPases in megakaryopoiesis
William Vainchenker1,2,3,4, Brahim Arkoun1,2,3,4, Francesca Basso-Valentina1,2,3,5
1INSERM, UMR 1287, Gustave Roussy, Equipe Labellisée LNCC, Villejuif, France.
Abstract:
Megakaryocytes (MKs) are the bone marrow (BM) cells that generate blood platelets by a process that requires: i) polyploidization responsible for the increased MK size and ii) cytoplasmic organization leading to extension of long pseudopods, called proplatelets, through the endothelial barrier to allow platelet release into blood. Low level of localized RHOA activation prevents actomyosin accumulation at the cleavage furrow and participates in MK polyploidization. In the platelet production, RHOA and CDC42 play opposite, but complementary roles. RHOA inhibits both proplatelet formation and MK exit from BM, whereas CDC42 drives the development of the demarcation membranes and MK migration in BM. Moreover, the RhoA or Cdc42 MK specific knock-out in mice and the genetic alterations in their down-stream effectors in human induce a thrombocytopenia demonstrating their key roles in platelet production. A better knowledge of Rho-GTPase signalling is thus necessary to develop therapies for diseases associated with platelet production defects.Abbreviations: AKT: Protein Kinase BARHGEF2: Rho/Rac Guanine Nucleotide Exchange Factor 2ARP2/3: Actin related protein 2/3BM: Bone marrowCDC42: Cell division control protein 42 homologCFU-MK: Colony-forming-unit megakaryocyteCIP4: Cdc42-interacting protein 4mDIA: DiaphanousDIAPH1; Protein diaphanous homolog 1ECT2: Epithelial Cell Transforming Sequence 2FLNA: Filamin AGAP: GTPase-activating proteins or GTPase-accelerating proteinsGDI: GDP Dissociation InhibitorGEF: Guanine nucleotide exchange factorHDAC: Histone deacetylaseLIMK: LIM KinaseMAL: Megakaryoblastic leukaemiaMARCKS: Myristoylated alanine-rich C-kinase substrateMKL: Megakaryoblastic leukaemiaMLC: Myosin light chainMRTF: Myocardin Related Transcription FactorOTT: One-Twenty Two ProteinPACSIN2: Protein Kinase C And Casein Kinase Substrate In Neurons 2PAK: P21-Activated KinasePDK: Pyruvate Dehydrogenase kinasePI3K: Phosphoinositide 3-kinasePKC: Protein kinase CPTPRJ: Protein tyrosine phosphatase receptor type JRAC: Ras-related C3 botulinum toxin substrate 1RBM15: RNA Binding Motif Protein 15RHO: Ras homologousROCK: Rho-associated protein kinaseSCAR: Suppressor of cAMP receptorSRF: Serum response factorSRC: SarcTAZ: Transcriptional coactivator with PDZ motifTUBB1: Tubulin β1VEGF: Vascular endothelial growth factorWAS: Wiskott Aldrich syndromeWASP: Wiskott Aldrich syndrome proteinWAVE: WASP-family verprolin-homologous proteinWIP: WASP-interacting proteinYAP: Yes-associated protein.
Insights
Rho GTPases, specifically RHOA and CDC42, are crucial for megakaryocyte polyploidization and platelet production. Understanding their opposing roles is key to developing therapies for thrombocytopenia.
Area of Science:
- Hematology
- Cell Biology
- Molecular Signaling
Background:
- Megakaryocytes (MKs) in bone marrow (BM) produce platelets through polyploidization and proplatelet formation.
- Rho GTPases, including RHOA and CDC42, regulate MK size, cytoplasmic organization, and platelet release.
- Dysregulation of Rho GTPase signaling is implicated in thrombocytopenia.
Purpose of the Study:
- To elucidate the complementary and opposing roles of RHOA and CDC42 in megakaryocyte development and platelet production.
- To highlight the necessity of understanding Rho-GTPase signaling for therapeutic interventions in platelet disorders.
Main Methods:
- Analysis of RHOA's role in preventing actomyosin accumulation during MK polyploidization.
- Investigation of RHOA and CDC42's contrasting functions in proplatelet formation, MK migration, and BM exit.
- Examination of MK-specific knockout mice for RhoA or Cdc42 and human genetic alterations in downstream effectors.
Main Results:
- Low, localized RHOA activation promotes MK polyploidization by limiting actomyosin.
- RHOA inhibits proplatelet formation and MK egress from BM, while CDC42 promotes demarcation membrane development and MK migration.
- MK-specific knockout of RhoA or Cdc42 in mice, and human genetic defects in their effectors, lead to thrombocytopenia.
Conclusions:
- RHOA and CDC42 play critical, opposing yet complementary roles in megakaryocyte biology and platelet production.
- Genetic disruptions in RhoA or Cdc42 signaling pathways result in significant platelet production defects.
- Further research into Rho-GTPase signaling is essential for developing novel therapies for thrombocytopenia and related diseases.
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