Human thrombopoiesis depends on Protein kinase Cδ/protein kinase Cε functional couple

• Published in: Haematologica (Roma) 2016-07, Vol.101 (7), p.812-820
• Main Authors: Carubbi, Cecilia, Masselli, Elena, Martini, Silvia, Galli, Daniela, Aversa, Franco, Mirandola, Prisco, Italiano, Jr, Joseph E, Gobbi, Giuliana, Vitale, Marco
• Format: Article
• Language: English
• Subjects: Adult; Aged; bcl-2-Associated X Protein - genetics; bcl-2-Associated X Protein - metabolism; bcl-X Protein - genetics; bcl-X Protein - metabolism; Blood Platelets - metabolism; Cell Differentiation - genetics; Female; Gene Expression; Gene Expression Regulation; Humans; Male; Megakaryocytes - cytology; Megakaryocytes - metabolism; Middle Aged; Primary Myelofibrosis - blood; Primary Myelofibrosis - diagnosis; Primary Myelofibrosis - metabolism; Protein Binding; Protein Kinase C-delta - genetics; Protein Kinase C-delta - metabolism; Protein Kinase C-epsilon - genetics; Protein Kinase C-epsilon - metabolism; Thrombocythemia, Essential - blood; Thrombocythemia, Essential - diagnosis; Thrombocythemia, Essential - metabolism; Thrombopoiesis - genetics
• ISSN: 0390-6078; 1592-8721
• DOI: 10.3324/haematol.2015.137984

A deeper understanding of the molecular events driving megakaryocytopoiesis and thrombopoiesis is essential to regulate in vitro and in vivo platelet production for clinical applications. We previously documented the crucial role of PKCε in the regulation of human and mouse megakaryocyte maturation and platelet release. However, since several data show that different PKC isoforms fulfill complementary functions, we targeted PKCε and PKCδ, which show functional and phenotypical reciprocity, at the same time as boosting platelet production in vitro. Results show that PKCδ, contrary to PKCε, is persistently expressed during megakaryocytic differentiation, and a forced PKCδ down-modulation impairs megakaryocyte maturation and platelet production. PKCδ and PKCε work as a functional couple with opposite roles on thrombopoiesis, and the modulation of their balance strongly impacts platelet production. Indeed, we show an imbalance of PKCδ/PKCε ratio both in primary myelofibrosis and essential thrombocythemia, featured by impaired megakaryocyte differentiation and increased platelet production, respectively. Finally, we demonstrate that concurrent molecular targeting of both PKCδ and PKCε represents a strategy for in vitro platelet factories.