Fig. 1From: MIF/CXCR4 signaling axis contributes to survival, invasion, and drug resistance of metastatic neuroblastoma cells in the bone marrow microenvironmentGeneration and characterization of CMs mimicking the BM niche. A) Quantification of different cell populations in expanded BM cultures (n = 6) by flow cytometry (empty dot plots). Purified culture of BM-MSC (column bars) was used as positive control for stroma markers (CD90, CD105 and HLA-DR). B) Graphical scheme of CM’s production (left). In vitro image (10x objective) of cells used for CM’s production at 48 h (right). C) Cytokine Profile Array membranes of CM-NB, CM-BM, CM-BM/NB (left). Quantification of detected cytokines and chemokines represented as mean pixel density of duplicate spots (right). D) Extracellular MIF quantification by ELISA in CM-NB (n = 6), CM-BM (n = 5) and CM-BM/NB (n = 6), being LAN-1 square, SH-SY5Y rhomboid, and IMR5 a circleBack to article page