Time-lapsed video microscopy and confocal imaging were used to study the mi
gration of wild-type (WT) and mitogen-activated protein kinase-activated pr
otein kinase 2 (MK2)(-/-) mouse neutrophils in Zigmond chambers containing
fMLP gradients. Confocal images of polarized WT neutrophils showed an intra
cellular gradient of phospho-MK2 from the anterior to the posterior region
of the neutrophils. Compared with WT neutrophils, MK2(-/-) neutrophils show
ed a partial loss of directionality but higher migration speed. Immunoblott
ing experiments showed a lower protein level of p38 mitogen-activated prote
in kinase and a loss of fMLP-induced extracellular signal-related kinase ph
osphorylation in MK2(-/-) neutrophils. These results suggest that MK2 plays
an important role in the regulation of neutrophil migration and may also a
ffect other signaling molecules.