Figure 3
Figure 3. L428 and KM-H2 CD20+ cell populations exhibit high ALDH activity and clonogenic potential. (A) ALDH activity for the CD30+ and CD20+ subsets. The data represent the mean ± SEM of the MFI difference between Aldefluor-stained cells with and without DEAB from 8 separate experiments. (B) The initial plating of 500 ALDHhigh L428 cells produced 19.7 (± 9.5) colonies compared with 5.7 ± 11 colonies from 500 ALDHlow L428 cells (P = .3), and 500 ALDHhigh KM-H2 cells generated 33.3 ± 5.4 colonies compared with 20.7 ± 6.4 from 500 ALDHlow KM-H2 cells (P = .3). Upon secondary replating, the original 500 ALDHhigh L428 generated 251 ± 25.9 colonies compared with 53.6 + 12.9 from the ALDHlow L428 cells (P = .01), and the original 500 ALDHhigh KM-H2 cells produced 243.7 ± 32.3 colonies compared with 27.7 ± 16 ALDHlow KM-H2 cells (P = .03). The data represent the mean ± SEM of 3 separate experiments.

L428 and KM-H2 CD20+ cell populations exhibit high ALDH activity and clonogenic potential. (A) ALDH activity for the CD30+ and CD20+ subsets. The data represent the mean ± SEM of the MFI difference between Aldefluor-stained cells with and without DEAB from 8 separate experiments. (B) The initial plating of 500 ALDHhigh L428 cells produced 19.7 (± 9.5) colonies compared with 5.7 ± 11 colonies from 500 ALDHlow L428 cells (P = .3), and 500 ALDHhigh KM-H2 cells generated 33.3 ± 5.4 colonies compared with 20.7 ± 6.4 from 500 ALDHlow KM-H2 cells (P = .3). Upon secondary replating, the original 500 ALDHhigh L428 generated 251 ± 25.9 colonies compared with 53.6 + 12.9 from the ALDHlow L428 cells (P = .01), and the original 500 ALDHhigh KM-H2 cells produced 243.7 ± 32.3 colonies compared with 27.7 ± 16 ALDHlow KM-H2 cells (P = .03). The data represent the mean ± SEM of 3 separate experiments.

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