Figure 1
Figure 1. MCL cells with the highest ALDH activity have enhanced clonogenic capacity and are more quiescent than bulk cells. (A) ALDH analysis of the human MCL lines Granta 519, Jeko-1, and Rec-1 and a representative clinical specimen by flow cytometry. ALDH+ populations are defined by gating for live cells by forward side scatter and in parallel with diethylaminobenzaldehyde (DEAB)–treated controls. Positive gates are determined by DEAB-treated cells and set at 0.01% for DEAB controls. For the patient samples, MCL tumor cells were initially identified by gating for CD19+CD5+ cells. Values represent percentage within each gate. (B) Colony formation by 1000 ALDH+ or ALDHneg cells. (C) Cell cycle analysis of ALDH+ and ALDHneg Jeko-1 cells. Values represent percentage within each gate. (D) Frequency of ALDH+ and ALDHneg cells in G0/G1 (*P < .05; n = 3). SSC indicates side scatter; 7AAD indicates 7-amino-actinomycin D.

MCL cells with the highest ALDH activity have enhanced clonogenic capacity and are more quiescent than bulk cells. (A) ALDH analysis of the human MCL lines Granta 519, Jeko-1, and Rec-1 and a representative clinical specimen by flow cytometry. ALDH+ populations are defined by gating for live cells by forward side scatter and in parallel with diethylaminobenzaldehyde (DEAB)–treated controls. Positive gates are determined by DEAB-treated cells and set at 0.01% for DEAB controls. For the patient samples, MCL tumor cells were initially identified by gating for CD19+CD5+ cells. Values represent percentage within each gate. (B) Colony formation by 1000 ALDH+ or ALDHneg cells. (C) Cell cycle analysis of ALDH+ and ALDHneg Jeko-1 cells. Values represent percentage within each gate. (D) Frequency of ALDH+ and ALDHneg cells in G0/G1 (*P < .05; n = 3). SSC indicates side scatter; 7AAD indicates 7-amino-actinomycin D.

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