Fig. 1.
Fig. 1. Expression and functionality of CXCR4 on BM myeloma cells. / (A) Myeloma CD38hiCD45RA− BM cells and myeloma-derived cell lines were incubated with the anti-CXCR4 44.717.111 or control [C] P3X63 mAb and analyzed by flow cytometry. Results from 3 different CD38hiCD45RA− BM samples (upper panels) expressing low (left), medium (middle), or high (right) levels of CXCR4 is shown. (B) Myeloma CD38hiCD45RA− BM and NCI-H929 cells were preincubated without or with pertussis toxin (PTx) in DMEM/BSA 0.5% and allowed to migrate in Transwell chemotaxis chambers to medium alone or an SDF-1α–containing lower chamber. Results from 3 different MM-CD38hiCD45RA− BM samples expressing medium or high levels of CXCR4 are shown. Data represent the mean ± SD of duplicate samples. (C) Cells were incubated for the indicated times with SDF-1α (solid circles) or adhesion medium (open circles), stained with fluorescein isothiocyanate–phalloidin, and subjected to flow cytometry.

Expression and functionality of CXCR4 on BM myeloma cells.

(A) Myeloma CD38hiCD45RA BM cells and myeloma-derived cell lines were incubated with the anti-CXCR4 44.717.111 or control [C] P3X63 mAb and analyzed by flow cytometry. Results from 3 different CD38hiCD45RA BM samples (upper panels) expressing low (left), medium (middle), or high (right) levels of CXCR4 is shown. (B) Myeloma CD38hiCD45RA BM and NCI-H929 cells were preincubated without or with pertussis toxin (PTx) in DMEM/BSA 0.5% and allowed to migrate in Transwell chemotaxis chambers to medium alone or an SDF-1α–containing lower chamber. Results from 3 different MM-CD38hiCD45RA BM samples expressing medium or high levels of CXCR4 are shown. Data represent the mean ± SD of duplicate samples. (C) Cells were incubated for the indicated times with SDF-1α (solid circles) or adhesion medium (open circles), stained with fluorescein isothiocyanate–phalloidin, and subjected to flow cytometry.

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