Figure 3.
Figure 3. Lack of toxic and apoptotic effect on BM cells cocultured with HMCLs. Viability of BM-adherent cells in long-term cocultures with HMCLs (OPM2, XG-6, RPMI-8226, XG-1) was assessed after 21 days of coculture as described in “Patients, materials, and methods.” Graphs represent the percent mean ± SD of viable cells of 6 replicate wells. (A) MG63 cells treated with FAS (anti-CD95 mAb) were used as positive control for death cells. The presence of both death and apoptotic PreOBs has been investigated by flow cytometry after 48-hour coculture with XG-6 or OPM2 either in the presence or absence of a transwell insert using 7-amino-actinomycin D (7AAD) gating on all (B) CD138- cells and (C) Apo 2.7 mAb gating on viable CD138- cells. Any significant difference in the number of death or apoptotic PreOBs was not observed in the control and coculture condition.

Lack of toxic and apoptotic effect on BM cells cocultured with HMCLs. Viability of BM-adherent cells in long-term cocultures with HMCLs (OPM2, XG-6, RPMI-8226, XG-1) was assessed after 21 days of coculture as described in “Patients, materials, and methods.” Graphs represent the percent mean ± SD of viable cells of 6 replicate wells. (A) MG63 cells treated with FAS (anti-CD95 mAb) were used as positive control for death cells. The presence of both death and apoptotic PreOBs has been investigated by flow cytometry after 48-hour coculture with XG-6 or OPM2 either in the presence or absence of a transwell insert using 7-amino-actinomycin D (7AAD) gating on all (B) CD138- cells and (C) Apo 2.7 mAb gating on viable CD138- cells. Any significant difference in the number of death or apoptotic PreOBs was not observed in the control and coculture condition.

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