Figure 5.
Localization of GFP+ and mutant-BTK–expressing MEC-1 cells in mice. Tumors were established from MEC-1 cells harboring WT or mutant BTK, as described in Figure 4. (A-B) Representative flow cytometry plots for the spleen and bone marrow samples collected from mice with BTKWT (n = 4; left), BTKC481S (n = 9; center), and BTKC481R (n = 9; right). At the time of euthanization, cells were collected from the spleen (A) and bone marrow (B), stained with a monoclonal antibody against human CD19 to identify the GFP+ MEC-1 cells, and analyzed by flow cytometry. (C-D) The percentage of CD19+ MEC-1 cells in spleen (C) and bone marrow (D). One-way analysis of variance, P = .05; Student t test, *P < .05 for BTKWT vs BTKC481R cells; **P < .01 for BTKWT vs BTKC481S cells.

Localization of GFP+ and mutant-BTK–expressing MEC-1 cells in mice. Tumors were established from MEC-1 cells harboring WT or mutant BTK, as described in Figure 4. (A-B) Representative flow cytometry plots for the spleen and bone marrow samples collected from mice with BTKWT (n = 4; left), BTKC481S (n = 9; center), and BTKC481R (n = 9; right). At the time of euthanization, cells were collected from the spleen (A) and bone marrow (B), stained with a monoclonal antibody against human CD19 to identify the GFP+ MEC-1 cells, and analyzed by flow cytometry. (C-D) The percentage of CD19+ MEC-1 cells in spleen (C) and bone marrow (D). One-way analysis of variance, P = .05; Student t test, *P < .05 for BTKWT vs BTKC481R cells; **P < .01 for BTKWT vs BTKC481S cells.

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