Protein kinase C promotes restoration of calcium homeostasis to platelet activating factor-stimulated human neutrophils by inhibition of phospholipase C
<p>Abstract</p> <p>Background</p> <p>The role of protein kinase C (PKC) in regulating the activity of phospholipase C (PLC) in neutrophils activated with the chemoattractant, platelet-activating factor (PAF, 20 and 200 nM), was probed in the current study using the sele...
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BMC,
2009-10-01T00:00:00Z.
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Summary: | <p>Abstract</p> <p>Background</p> <p>The role of protein kinase C (PKC) in regulating the activity of phospholipase C (PLC) in neutrophils activated with the chemoattractant, platelet-activating factor (PAF, 20 and 200 nM), was probed in the current study using the selective PKC inhibitors, GF10903X (0.5 - 1 μM) and staurosporine (400 nM).</p> <p>Methods</p> <p>Alterations in cytosolic Ca<sup>2+</sup>, Ca<sup>2+ </sup>influx, inositol triphosphate (IP<sub>3</sub>), and leukotriene B<sub>4 </sub>production were measured using spectrofluorimetric, radiometric and competitive binding radioreceptor and immunoassay procedures, respectively.</p> <p>Results</p> <p>Activation of the cells with PAF was accompanied by an abrupt increase in cytosolic Ca<sup>2+ </sup>followed by a gradual decline towards basal levels. Pretreatment of neutrophils with the PKC inhibitors significantly increased IP<sub>3 </sub>production with associated enhanced Ca<sup>2+ </sup>release from storage vesicles, prolongation of the peak cytosolic Ca<sup>2+ </sup>transients, delayed clearance and exaggerated reuptake of the cation, and markedly increased synthesis of LTB<sub>4</sub>. The alterations in Ca<sup>2+ </sup>fluxes observed with the PKC inhibitors were significantly attenuated by U73122, a PLC inhibitor, as well as by cyclic AMP-mediated upregulation of the Ca<sup>2+</sup>-resequestering endomembrane ATPase.</p> <p>Taken together, these observations are compatible with a mechanism whereby PKC negatively modulates the activity of PLC, with consequent suppression of IP<sub>3 </sub>production and down-regulation of Ca<sup>2+ </sup>mediated pro-inflammatory responses of PAF-activated neutrophils.</p> <p>Conclusion</p> <p>Although generally considered to initiate and/or amplify intracellular signalling cascades which activate and sustain the pro-inflammatory activities of neutrophils and other cell types, the findings of the current study have identified a potentially important physiological, anti-inflammatory function for PKC, at least in neutrophils.</p> |
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Item Description: | 10.1186/1476-9255-6-29 1476-9255 |