GTP-dependent secretion from neutrophils is regulated by Cdk5.
We have previously shown evidence for the existence of a calcium-independent, GTP-regulated mechanism of secretion from neutrophils, but this secretory mechanism remains to be fully elucidated. Cyclin-dependent kinase 5 ( Cdk5), the various substrates of which include Munc18 and synapsin 1, has been implicated in neuronal secretion. Although the Cdk5 activator, p35, and Cdk5- p35 activity are primarily associated with neurons, we report here that p35 also exists in neutrophils and that an active Cdk5- p35 complex is present in these cells. Cdk5- p35 activity in human neutrophils is mostly localized in secretory granules, which show an increase in Cdk5- p35 level and activity upon GTP stimulation. The potent Cdk5 inhibitor, roscovitine, completely blocks GTP-stimulated granule Cdk5 activity, which accompanies lactoferrin secretion from neutrophil-specific granules. Roscovitine also inhibits GTP-induced lactoferrin secretion and surface localization of the secretion markers, CD63 and CD66b, to a certain extent. Furthermore, neutrophils from wild-type mice treated with roscovitine and neutrophils from p35(-/-) mice exhibit comparable surface expression levels of both CD63 and CD66b upon GTP stimulation. Although our data suggest that other molecules control GTP-induced secretion from neutrophils, it is clear that Cdk5- p35 is required to elicit the maximum GTP-induced secretory response. Our observation that multiple proteins in neutrophil granules serve as specific substrates of Cdk5 further supports the premise that the kinase is a key component of the GTP-regulated secretory apparatus in neutrophils.[1]References
- GTP-dependent secretion from neutrophils is regulated by Cdk5. Rosales, J.L., Ernst, J.D., Hallows, J., Lee, K.Y. J. Biol. Chem. (2004) [Pubmed]
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