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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: Gene Ther. 2014 Jan 16;21(3):289–297. doi: 10.1038/gt.2013.84

Figure 4. Tumor Targeting, antibody production, and induction of apoptosis in vivo.

Figure 4

(A, B) Recovery of viable viral particles from tumor, liver, lung, heart, spleen and brain from mice at day 5 (A) and Day 28 (B) after virus treatment (n=5 mice per group). Tissues were processed and assays were preformed as in methods. Viral titers are displayed as TCID50/gram of tissue . Arrow represents the assay's limit of detection-LOD (1.26×102 TCID50/gram of tissue). (C) Immunocompetent (Balb/c) mice (n = 3 per group) bearing 4T1 tumors received two intravenous injections of either PBS or MV-m-uPA (1.5×106 TCID50). Tumors were harvested 3 days later and frozen tumor sections were used for immunostaining for measles N protein. Viral protein was detected in tumors after intravenous administration of the virus. TUNEL assay of tumors from mice treated with MV-m-uPA or PBS was performed as in materials and methods (n=3 per group). Scale bar = 200 μm. (D) Quantitative analysis of TUNEL–positive nuclei in 4 microscopic fields per section per sample (displayed as percentage of positive/total nuclei; n = 3 per group). *, P < 0.01, MV-m-uPA versus ctrl.