Figure 5
Figure 5. Marrow stromal cells protect MCL cells from 4-HC-induced cytotoxicity. The mean viability of SP-53 cells (A) and MINO cells (B) treated with 4-HC is presented at the different time points displayed on the horizontal axis. MCL cell viability was increased when MCL cells were cocultured with M2-10B4 (), compared with MCL in suspension and without stromal cell support (). Results are presented as mean relative viability compared with untreated controls (100%) and are the mean ± SEM of triplicates. *Protection of MCL cells from 4-HC-induced cytotoxicity with significantly higher viabilities compared with controls (P < .05). (C) Contour plots that depict the viability of MINO MCL cells, as detected by staining with DiOC6 and PI after 24 hours of culture with 10 μM 4-HC, in the presence or absence of M2-10B4 stromal cells, as indicated above each of the plots. The proportion of viable cells is indicated above each of the gates that define viable cells by bright DiOC6 staining and PI exclusion.

Marrow stromal cells protect MCL cells from 4-HC-induced cytotoxicity. The mean viability of SP-53 cells (A) and MINO cells (B) treated with 4-HC is presented at the different time points displayed on the horizontal axis. MCL cell viability was increased when MCL cells were cocultured with M2-10B4 (), compared with MCL in suspension and without stromal cell support (). Results are presented as mean relative viability compared with untreated controls (100%) and are the mean ± SEM of triplicates. *Protection of MCL cells from 4-HC-induced cytotoxicity with significantly higher viabilities compared with controls (P < .05). (C) Contour plots that depict the viability of MINO MCL cells, as detected by staining with DiOC6 and PI after 24 hours of culture with 10 μM 4-HC, in the presence or absence of M2-10B4 stromal cells, as indicated above each of the plots. The proportion of viable cells is indicated above each of the gates that define viable cells by bright DiOC6 staining and PI exclusion.

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