Expression of mRNA for the C-X-C chemokine, macrophage inflammatory pr
otein-2 (MIP-2), is induced during acute inflammation in rat models of
disease. We have characterized the phlogistic potential of rat recomb
inant MIP-2 (rMIP-2) protein in vitro and in vivo. Recombinant MIP-2 c
aused marked PMN chemotaxis in vitro, with peak chemotactic activity a
t 10 nM. Incubation of whole blood with rMIP-2 caused a significant lo
ss of L-selectin and a significant increase in Mac-1 expression on the
PMN surface. Under similar conditions rMIP-2 also caused a modest res
piratory burst in PMNs. The intratracheal instillation of 10 and 50 mu
g of rMIP-2 caused a significant influx of PMNs into the airspace of
the lungs. Rat MIP-2 is a potent neutrophil chemotactic factor capable
of causing neutrophil activation and is likely to function in PMN rec
ruitment during acute inflammation in rat disease models.