Journal
BMC CELL BIOLOGY
Volume 11, Issue -, Pages -Publisher
BMC
DOI: 10.1186/1471-2121-11-52
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Funding
- Swedish Society for Medical Research
- Swedish Medical Research Council
- Inga Lisa and Arne Lundberg foundation
- King Gustaf V 80-Year Foundation
- Swedish state
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Background: The molecular basis for neutrophil recognition of chemotactic peptides is their binding to specific G-protein- coupled cell surface receptors (GPCRs). Human neutrophils express two pattern recognition GPCRs, FPR1 and FPR2, which belong to the family of formyl peptide receptors. The high degree of homology between these two receptors suggests that they share many functional and signal transduction properties, although they exhibit some differences with respect to signaling. The aims of this study were to determine whether FPR2 triggers a unique signal that allows direct influx of extracellular calcium without the emptying of intracellular calcium stores, and whether the gelsolin-derived PIP2-binding peptide, PBP10, selectively inhibits FPR2-mediated transient rise in intracellular Ca-2(+). Results: The transient rise in intracellular Ca-2(+) induced by agonists for FPR1 or FPR2 in human neutrophils occurred also in the presence of a chelator of Ca-2(+) (EGTA). PBP10 inhibited not only FPR2-induced oxidase activity, but also the transient rise in intracellular Ca-2(+). Conclusions: Ca-2(+) signaling mediated via FPR2 follows the same route as FPR1, which involves initial emptying of the intracellular stores. PBP10 inhibits selectively the signals generated by FPR2, both with respect to NADPH-oxidase activity and the transient rise in intracellular Ca-2(+) induced by agonist exposure.
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