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. Author manuscript; available in PMC: 2016 Jan 15.
Published in final edited form as: Cancer Res. 2015 May 14;75(14):2811–2821. doi: 10.1158/0008-5472.CAN-14-3761

Fig.5. Cytokine release by murine peritoneal macrophages is β3 integrin-dependent.

Fig.5

Peritoneal cells from female WT and β3−/− mice were pooled for each genotype and assessed by multichannel FACS. Experiments were carried out in triplicate and data are presented as mean±SD (n=4-24).

A. Expression of macrophage cell surface markers (**p<0.01).

B. Expression of the adenoviral receptors, CAR, β3 and β5 (***p<0.001).

C. Murine peritoneal cells were treated ex vivo with dl922-947 (10,000vp/cell) or vehicle. Cytokine protein in supernatants was quantified at 1 and 6 hours. Change over time was compared in WT and β3−/− peritoneal cells. (**p<0.01, ***p<0.001). KC=keratinocyte chemoattractant

D. Murine peritoneal cells were pooled and treated ex vivo with dl922-947 (10,000vp/cell) alone or in combination with the β3 inhibitor, H2574 (20μM). Cytokine protein is shown at 6 hours relative to 1 hour (*p<0.05, ***p<0.001, ns=non-significant). KC=keratinocyte chemoattractant