Figure 2
Figure 2. Basic characterization of transgenic mice. (A) H&E staining (left) and B220 immunohistochemistry of WT and EZH2Y641F mice. (B) Spleen weights of mice transgenic for EZH2Y641F and WT control mice analyzed at different ages. (C) Immunophenotypic analysis of bone marrow cells of EZH2Y641F mice (n = 16) or WT controls (n = 13). (D) Immunophenotypic analysis of spleen cells of EZH2Y641F mice (n = 7) or WT controls (n = 5). Means and standard deviation of the percentages of cells carrying the respective marker are shown. No significant differences were observed. (E) Immunophenotypic analysis of the GC B-cell compartment in the spleen of aged (60-62 weeks), nonimmunized EZH2Y641F mice (n = 5) or WT controls (n = 5) using GL7 and FAS (upper) and CD38 and FAS (lower) (P = .003). Representative flow cytometric plots are shown to the right. Statistical analysis was performed using an unpaired Student t test with Welch’s correction. H&E, hematoxylin and eosin.

Basic characterization of transgenic mice. (A) H&E staining (left) and B220 immunohistochemistry of WT and EZH2Y641F mice. (B) Spleen weights of mice transgenic for EZH2Y641F and WT control mice analyzed at different ages. (C) Immunophenotypic analysis of bone marrow cells of EZH2Y641F mice (n = 16) or WT controls (n = 13). (D) Immunophenotypic analysis of spleen cells of EZH2Y641F mice (n = 7) or WT controls (n = 5). Means and standard deviation of the percentages of cells carrying the respective marker are shown. No significant differences were observed. (E) Immunophenotypic analysis of the GC B-cell compartment in the spleen of aged (60-62 weeks), nonimmunized EZH2Y641F mice (n = 5) or WT controls (n = 5) using GL7 and FAS (upper) and CD38 and FAS (lower) (P = .003). Representative flow cytometric plots are shown to the right. Statistical analysis was performed using an unpaired Student t test with Welch’s correction. H&E, hematoxylin and eosin.

Close Modal

or Create an Account

Close Modal
Close Modal