Figure 5.
Figure 5. CXCL12 treatment results in prolonged activation of ERK in ZAP-70+ but not ZAP-70– CLL B cells. (A) Lysates were collected from CLL B cells treated for varying times with CXCL12 (100 ng/mL). Western blots were probed with an anti–phospho-p44/42 ERK (P-ERK) antibody (top panel) and then with an anti-p44/42 ERK (T-ERK) antibody to demonstrate loading (bottom panel). (i) ZAP-70+ PB CLL cells. (ii) ZAP-70– PB CLL cells. (B) Densitometric quantification of P-ERK and T-ERK Western blots from 7 ZAP-70+ and 7 ZAP-70– patients was carried out and the ratio of P-ERK to T-ERK was calculated to normalize for loading. Results are presented as mean ± SEM (Student 2-sample 2-tailed t test). (C) ERK activation following addition of CXCL12 in ZAP-70+ CLL B cells is sustained for up to 2 hours.

CXCL12 treatment results in prolonged activation of ERK in ZAP-70+ but not ZAP-70 CLL B cells. (A) Lysates were collected from CLL B cells treated for varying times with CXCL12 (100 ng/mL). Western blots were probed with an anti–phospho-p44/42 ERK (P-ERK) antibody (top panel) and then with an anti-p44/42 ERK (T-ERK) antibody to demonstrate loading (bottom panel). (i) ZAP-70+ PB CLL cells. (ii) ZAP-70 PB CLL cells. (B) Densitometric quantification of P-ERK and T-ERK Western blots from 7 ZAP-70+ and 7 ZAP-70 patients was carried out and the ratio of P-ERK to T-ERK was calculated to normalize for loading. Results are presented as mean ± SEM (Student 2-sample 2-tailed t test). (C) ERK activation following addition of CXCL12 in ZAP-70+ CLL B cells is sustained for up to 2 hours.

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