Figure 5.
Figure 5. Plasma MPs and tumor growth in Par4 KO mice. (A) Plasma MPs from WT and Par4 KO mice were analyzed by nanoparticle tracking, and are shown ± SEM (n = 6); P < .03. (B) A total of 1 × 106 LLC cells were seeded in the flanks of WT and Par4 KO mice, and tumor volumes were measured 8 days after seeding, shown ± SEM (n = 6); P < .03. (C) LLC tumors were seeded as in panel B, and 1 × 1010 freshly isolated PMPs were transfused in the tail vein every 24 hours beginning at day 8 as indicated. Tumor volumes were measured daily, and are shown ± SEM (n = 6); *P < .03; **P < .002. (D) Tumors from panel C were resected, fixed, and processed for IHC with antibodies to murine CD41 (αIIb integrin, red) to label endogenous PMPs, and cleaved caspase-3 (green); DAPI stain is shown in blue. (E) Tumor sections from panel C stained with antibodies to human CD41 (αIIb integrin, red) to label transfused PMPs, cleaved caspase-3 (cl. cas-3, green), and DAPI (blue). Bars, 15 μm.

Plasma MPs and tumor growth in Par4 KO mice. (A) Plasma MPs from WT and Par4 KO mice were analyzed by nanoparticle tracking, and are shown ± SEM (n = 6); P < .03. (B) A total of 1 × 106 LLC cells were seeded in the flanks of WT and Par4 KO mice, and tumor volumes were measured 8 days after seeding, shown ± SEM (n = 6); P < .03. (C) LLC tumors were seeded as in panel B, and 1 × 1010 freshly isolated PMPs were transfused in the tail vein every 24 hours beginning at day 8 as indicated. Tumor volumes were measured daily, and are shown ± SEM (n = 6); *P < .03; **P < .002. (D) Tumors from panel C were resected, fixed, and processed for IHC with antibodies to murine CD41 (αIIb integrin, red) to label endogenous PMPs, and cleaved caspase-3 (green); DAPI stain is shown in blue. (E) Tumor sections from panel C stained with antibodies to human CD41 (αIIb integrin, red) to label transfused PMPs, cleaved caspase-3 (cl. cas-3, green), and DAPI (blue). Bars, 15 μm.

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