Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Moog, Sylvie et al., 2025
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/222235

Importance of tubulin detyrosination in platelet biogenesis

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

Background: The functional diversity of microtubules is regulated through the expression of distinct x-and p-tubulin isotypes together with several posttranslational modifications, a concept known as tubulin code. Tubulin detyrosination is a reversible posttranslational modification that consists of the removal of the genetically encoded C-terminal tyrosine residue of most x-tubulins. While this modification has been observed in the megakaryocyte lineage, its importance remains poorly understood in platelet biogenesis. Objectives: To assess the role of x-tubulin detyrosination in platelet biogenesis. Methods: The responsible enzymes and the relative abundance of detyrosinated x-tubulins were monitored by quantitative reverse transcription-polymerase chain reaction and Western blotting, respectively, in human cultured megakaryocytes and platelets differentiated from CD34+ hematopoietic stem and progenitor cells. The function of x-tubulin detyrosination was assessed in human cultured megakaryocytes treated with the VASH-SVBP inhibitor EpoY, and in mice constitutively inactivated for Svbp (which encodes the cofactor of the VASH detyrosinases). Results: Transcriptional analysis identified VASH1-SVBP and MATCAP as the predominant detyrosinases in the megakaryocyte lineage. During megakaryocyte maturation, their transcript levels progressively increased and correlated with the accumulation of detyrosinated alpha-tubulins. Remarkably, inhibition of VASH1-SVBP by EpoY abolished tubulin detyrosination, establishing VASH1-SVBP as the main functional detyrosinase in megakaryocytes. More importantly, EpoY enhanced proplatelet formation and platelet production in vitro. These in vitro data were confirmed in vivo in SVBP-deficient mice, which exhibited an increase in platelet counts. Conclusion: These findings reveal, for the first time, a role for tubulin detyrosination in proplatelet formation, thereby expanding our understanding of the megakaryocyte tubulin code beyond tubulin isotypes.

Citació

Citació

MOOG, Sylvie, MALLO, Léa, ECKLY, Anita, JANKE, Carsten, PUJOL, Aurora, IRUZUBIETA, Pablo, LÓPEZ DE MUNAIN, Adolfo, MOUTIN, Marie jo, STRASSEL, Catherine, LANZA, François, KIMMERLIN, Quentin. Importance of tubulin detyrosination in platelet biogenesis. _Journal of Thrombosis and Haemostasis_. 2025. Vol. 23, núm. 6, pàgs. 2025-2034. [consulta: 21 de gener de 2026]. ISSN: 1538-7836. [Disponible a: https://hdl.handle.net/2445/222235]

Exportar metadades

JSON - METS

Compartir registre