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. Author manuscript; available in PMC: 2014 Jun 23.
Published in final edited form as: Cancer Res. 2011 Apr 21;71(11):3831–3840. doi: 10.1158/0008-5472.CAN-10-4002

Figure 2. The effect of stromal cells on the atiprimod-induced apoptosis of cells expressing mutant JAK2V617F.

Figure 2

(A) FDCP-EpoRV617F cells were cultured alone (control), or with atiprimod, with or without HS5 stromal cells. Following 48 hour culture cells were harvested, stained with annexing V and percentage of apoptotic cells determined by flow cytometry. Data from representative experiment are shown. Atiprimod-induced apoptosis was dramatically impaired when JAK2V617F-positive cells were co-cultured with stromal cells (B) FDCP-EpoRV617F and SET-2 cells were cultured without (control) or with three different stromal cell monolayers (HS5, NK.tert, TM-R1) in the absence or presence of atiprimod for 48 hours. The induction of apoptosis was then assessed by flow cytometry. Results represent the mean ± SD from 3 independent experiments.