Author/Authors :
Reynaud، نويسنده , , Damien and Pietras، نويسنده , , Eric and Barry-Holson، نويسنده , , Keegan and Mir، نويسنده , , Alain and Binnewies، نويسنده , , Mikhail and Jeanne، نويسنده , , Marion and Sala-Torra، نويسنده , , Olga and Radich، نويسنده , , Jerald P. and Passegué، نويسنده , , Emmanuelle، نويسنده ,
Abstract :
Summary
a mouse model recapitulating the main features of human chronic myelogenous leukemia (CML), we uncover the hierarchy of leukemic stem and progenitor cells contributing to disease pathogenesis. We refine the characterization of CML leukemic stem cells (LSCs) to the most immature long-term hematopoietic stem cells (LT-HSCs) and identify some important molecular deregulations underlying their aberrant behavior. We find that CML multipotent progenitors (MPPs) exhibit an aberrant B-lymphoid potential but are redirected toward the myeloid lineage by the action of the proinflammatory cytokine IL-6. We show that BCR/ABL activity controls Il-6 expression thereby establishing a paracrine feedback loop that sustains CML development. These results describe how proinflammatory tumor environment affects leukemic progenitor cell fate and contributes to CML pathogenesis.