Figure 7
Figure 7. Loss of endogenous Bcl-2 does not reduce the severity of Eμ-myc lymphoma. (A) Comparison at time of death of spleen weights (g) from moribund Eμ-myc (n = 8), Eμ-myc/bcl-2−/− (n = 10), and normal control (wt) reconstituted mice (n = 4), and of peripheral leukocyte cellularity (× 106 cells/mL) from moribund Eμ-myc (n = 8), Eμ-myc/bcl-2−/− (n = 9), and normal control (wt) (n = 9) reconstituted mice. Bars indicate the mean values. (B) Hematoxylin/eosin staining of representative LN (×40), bone marrow (×20), and liver (×20) sections taken from terminally ill Eμ-myc and Eμ-myc/bcl-2−/− reconstituted animals. Images were visualized using an Olympus BX50 microscope (Olympus, Tokyo, Japan) equipped with a 40×/0.85 NA or a 20×/0.5 NA objective. Images were photographed with an Olympus U-HAD3 digital camera and recorded using Axiovision 4.2 software (Carl Zeiss, Thornwood, NY). Images were processed with Adobe Photoshop CS2 software, version 9.0 (Adobe Systems, San Jose, CA).

Loss of endogenous Bcl-2 does not reduce the severity of Eμ-myc lymphoma. (A) Comparison at time of death of spleen weights (g) from moribund Eμ-myc (n = 8), Eμ-myc/bcl-2−/− (n = 10), and normal control (wt) reconstituted mice (n = 4), and of peripheral leukocyte cellularity (× 106 cells/mL) from moribund Eμ-myc (n = 8), Eμ-myc/bcl-2−/− (n = 9), and normal control (wt) (n = 9) reconstituted mice. Bars indicate the mean values. (B) Hematoxylin/eosin staining of representative LN (×40), bone marrow (×20), and liver (×20) sections taken from terminally ill Eμ-myc and Eμ-myc/bcl-2−/− reconstituted animals. Images were visualized using an Olympus BX50 microscope (Olympus, Tokyo, Japan) equipped with a 40×/0.85 NA or a 20×/0.5 NA objective. Images were photographed with an Olympus U-HAD3 digital camera and recorded using Axiovision 4.2 software (Carl Zeiss, Thornwood, NY). Images were processed with Adobe Photoshop CS2 software, version 9.0 (Adobe Systems, San Jose, CA).

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