Figure 4
Figure 4. Mechanisms underlying trafficking of aged neutrophils during inflammation. Using multichannel flow cytometry, numbers of aged and nonaged neutrophils in bone marrow, blood, and lysates of different organs of WT, TLR-2−/−, or TLR-4-mutant mice and of WT mice receiving intra-arterial injections of the CXCR4 inhibitor AMD3100, blocking anti-CXCL12 mAbs, the TLR-4 inhibitor TAK-242, or drug vehicle/isotype control antibodies upon IP injection of PBS or LPS were quantitatively analyzed as detailed in “Methods.” Results that have been normalized to controls are shown. Mean ± SEM for n = 4-5; #P < .05 vs PBS; *P < .05 vs drug vehicle/isotype control/WT.

Mechanisms underlying trafficking of aged neutrophils during inflammation. Using multichannel flow cytometry, numbers of aged and nonaged neutrophils in bone marrow, blood, and lysates of different organs of WT, TLR-2−/−, or TLR-4-mutant mice and of WT mice receiving intra-arterial injections of the CXCR4 inhibitor AMD3100, blocking anti-CXCL12 mAbs, the TLR-4 inhibitor TAK-242, or drug vehicle/isotype control antibodies upon IP injection of PBS or LPS were quantitatively analyzed as detailed in “Methods.” Results that have been normalized to controls are shown. Mean ± SEM for n = 4-5; #P < .05 vs PBS; *P < .05 vs drug vehicle/isotype control/WT.

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