Figure 6
Figure 6. Role of LFA, PECAM-1, ICAM-2, and VCAM-1 for CXCL1- or PAF-elicited leukocyte responses. (A-B) Leukocyte rolling, (C-D) firm adherence, and (E-F) transmigration were quantified in postcapillary venules of the cremaster muscle using RLOT in vivo microscopy as detailed in “Quantification of leukocyte kinetics and microhemodynamic parameters.” Panels show results for PBS-treated WT control mice as well as for WT mice receiving blocking mAbs directed against LFA-1, PECAM-1 (clone Mec13.3), ICAM-2, and VCAM-1 or isotype control and a nonblocking anti–PECAM-1 mAb (clone 390) after stimulation with CXCL1 or PAF (mean ± SEM for n = 4 per group; #P < .05, vs unstimulated; *P < .05, vs isotype control).

Role of LFA, PECAM-1, ICAM-2, and VCAM-1 for CXCL1- or PAF-elicited leukocyte responses. (A-B) Leukocyte rolling, (C-D) firm adherence, and (E-F) transmigration were quantified in postcapillary venules of the cremaster muscle using RLOT in vivo microscopy as detailed in “Quantification of leukocyte kinetics and microhemodynamic parameters.” Panels show results for PBS-treated WT control mice as well as for WT mice receiving blocking mAbs directed against LFA-1, PECAM-1 (clone Mec13.3), ICAM-2, and VCAM-1 or isotype control and a nonblocking anti–PECAM-1 mAb (clone 390) after stimulation with CXCL1 or PAF (mean ± SEM for n = 4 per group; #P < .05, vs unstimulated; *P < .05, vs isotype control).

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