ArrayExpress Uploader0mousePBSMIF8584arrayexpress_sid8Lasting B-cell persistence depends on survival signals that are transduced by cell surface receptors. Here, we describe a novel...E-GEOD-33352/profile/8773/arrayexpressuploader12cellchronic lymphocytic leukemiacytokineheparinleukemiaperipheralproteoglycansurfacetyrosineDec.12, 2014Falsegene-regulation-following-mif-stimulationE-GEOD-33352_A-AFFY-36Gene regulation following MIF stimulation.Nov.24, 2014Lasting B-cell persistence depends on survival signals that are transduced by cell surface receptors. Here, we describe a novel biological mechanism essential for survival and homeostasis of normal peripheral mature B cells and chronic lymphocytic leukemia (CLL) cells, regulated by the heparin-binding cytokine, midkine (MK), and its proteoglycan receptor, the receptor-type tyrosine phosphatase zeta (RPTPζ). We demonstrate that MK initiates a signaling cascade leading to B cell survival, by binding to RPTPζ. In mice lacking PTPRZ, the proportion and number of the mature B cell population is reduced. Our results emphasize a unique and critical function for MK signaling in the previously described MIF/CD74 induced survival pathway. Stimulation of CD74 with MIF leads to c-Met activation, resulting in elevation of MK expression in both normal mouse splenic B and CLL cells. Our results indicate that MK and RPTPζ are important regulators of the B cell repertoire. These findings could pave the way towards understanding the mechanisms shaping B cell survival, and suggest novel therapeutic strategies based on the blockade of the midkine/RPTPζ-dependent survival pathway. 2 samples were incubated with or without MIF.http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-33352http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-33352/samples/