Table 1

Effects on rolling neutrophils in cremaster muscles

Rolling cells/min
Velocity of rolling cells, μm/s
0 min30 min60 min90 min0 min30 min60 min90 min
MIP-2 SF         
    WT (n = 7) 41 ± 11 22 ± 6 16 ± 4 14 ± 4* 41 ± 11 34 ± 6 31 ± 5 31 ± 6 
    hpa-tg (n = 7) 49 ± 7 31 ± 5 22 ± 4* 17 ± 3* 42 ± 7 37 ± 7 38 ± 8 31 ± 5 
    WT + heparin (n = 5) 40 ± 8 35 ± 9 35 ± 9 35 ± 9 39 ± 5 49 ± 6 48 ± 6 54 ± 5 
MIP-2 gel         
    WT (n = 5) 50 ± 9 30 ± 5 23 ± 4* 19 ± 4* 23 ± 4 25 ± 5 21 ± 3 21 ± 3 
Rolling cells/min
Velocity of rolling cells, μm/s
0 min30 min60 min90 min0 min30 min60 min90 min
MIP-2 SF         
    WT (n = 7) 41 ± 11 22 ± 6 16 ± 4 14 ± 4* 41 ± 11 34 ± 6 31 ± 5 31 ± 6 
    hpa-tg (n = 7) 49 ± 7 31 ± 5 22 ± 4* 17 ± 3* 42 ± 7 37 ± 7 38 ± 8 31 ± 5 
    WT + heparin (n = 5) 40 ± 8 35 ± 9 35 ± 9 35 ± 9 39 ± 5 49 ± 6 48 ± 6 54 ± 5 
MIP-2 gel         
    WT (n = 5) 50 ± 9 30 ± 5 23 ± 4* 19 ± 4* 23 ± 4 25 ± 5 21 ± 3 21 ± 3 

WT, hpa-tg, or WT mice pretreated with heparin (close intra-arterially, 0.5 mg/mouse) were monitored during MIP-2 superfusion (0.5nM) or after placement of an MIP-2–containing gel (0.5μM) at a distance of 400 μm from the observed venule. Values are mean ± SEM.

*

P < .05 vs t = 0.

P < .05 vs WT activated by MIP-2 superfusion.

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