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. 2019 Oct 15;39(6):1185–1197. doi: 10.1038/s41388-019-1053-6

Fig. 5.

Fig. 5

OMP-52M51 inhibits DLL4-induced CXCR4 expression and migration. Primary cells from NOTCH1-mutated and NOTCH1-unmutated CLL cases were pretreated for 2 h with OMP-52M51 before DLL4 stimulation (4 μg/mL) for 48 h. a CXCR4 expression was analyzed by quantitative real time PCR. mRNA relative levels are given as arbitrary units, using untreated cells as a reference. b CXCR4 expression was analyzed by flow cytometry (n = 4 NOTCH1-mutated cells; n = 4 NOTCH1-unmutated cells). CXCR4 expression levels are showed based on the median fluorescence intensity (MFI) on viable cell population, using untreated cells as a reference. c Samples were assayed for chemotaxis toward CXCL12 (200 ng/ml). Migration is represented as the percentage of migrating cells out of total viable cells added to the transwell. Control: isotype control. Bars represent the mean ± SEM of NOTCH1-mutated (n = 8) and -unmutated (n = 4) CLL cases. *p < 0.05; **p < 0.01. d Samples were assayed for chemotaxis toward CXCL13 (500 ng/ml). Migration is represented as the percentage of migrating cells out of total viable cells added to the transwell. Bars represent the mean ± SEM of NOTCH1-mutated CLL cases (n = 6). *p < 0.05