TY - JOUR AU - Anita Roy, AU - Larissa Lordier, AU - Catherine Pioche-Durieu, AU - Sylvie Souquere, AU - Lydia Roy, AU - Philippe Rameau, AU - Valérie Lapierre, AU - Eric Le Cam, AU - Isabelle Plo, AU - Najet Debili, AU - Hana Raslova, AU - William Vainchenker, PY - 2016/11/30 Y2 - 2024/03/29 TI - Uncoupling of the Hippo and Rho pathways allows megakaryocytes to escape the tetraploid checkpoint JF - Haematologica JA - haematol VL - 101 IS - 12 SE - Articles DO - 10.3324/haematol.2016.149914 UR - https://haematologica.org/article/view/7903 SP - 1469-1478 AB - Megakaryocytes are naturally polyploid cells that increase their ploidy by endomitosis. However, very little is known regarding the mechanism by which they escape the tetraploid checkpoint to become polyploid. Recently, it has been shown that the tetraploid checkpoint was regulated by the Hippo-p53 pathway in response to a downregulation of Rho activity. We therefore analyzed the role of Hippo-p53 pathway in the regulation of human megakaryocyte polyploidy. Our results revealed that Hippo-p53 signaling pathway proteins are present and are functional in megakaryocytes. Although this pathway responds to the genotoxic stress agent etoposide, it is not activated in tetraploid or polyploid megakaryocytes. Furthermore, Hippo pathway was observed to be uncoupled from Rho activity. Additionally, polyploid megakaryocytes showed increased expression of YAP target genes when compared to diploid and tetraploid megakaryocytes. Although p53 knockdown increased both modal ploidy and proplatelet formation in megakaryocytes, YAP knockdown caused no significant change in ploidy while moderately affecting proplatelet formation. Interestingly, YAP knockdown reduced the mitochondrial mass in polyploid megakaryocytes and decreased expression of PGC1α, an important mitochondrial biogenesis regulator. Thus, the Hippo pathway is functional in megakaryocytes, but is not induced by tetraploidy. Additionally, YAP regulates the mitochondrial mass in polyploid megakaryocytes. ER -