Regulation of calcium homeostasis in activated human neutrophils--potential targets for anti-inflammatory therapeutic strategies
Tintinger, G.R.; Anderson, R.; Ker, J.A.
South African Medical Journal 92(12): 990-996
2002
ISSN/ISBN: 0256-9574 PMID: 12561417 Document Number: 544192
The objectives of the current study were to: (i) present an integrated model for the restoration of calcium homeostasis in activated human neutrophils based on current knowledge and recent research; and (ii) identify potential targets for the modulation of calcium fluxes in activated neutrophils based on this model and to investigate the effects of intracellular probes which target key processes involved in calcium homeostasis and pro-inflammatory activity in these cells. Laboratory-based experimental research using purified human neutrophils from healthy, adult human volunteers. Calcium metabolism and pro-inflammatory activity of neutrophils. Modulation of calcium fluxes in activated human neutrophils can be achieved by cAMP-dependent upregulation of the activity of the endomembrane Ca(2+)-ATPase which resequesters cytosolic Ca2+. Formoterol, a long-acting beta 2-agonist, elevates intracellular cAMP levels, accelerates Ca2+ restoration in activated neutrophils and downregulates the pro-inflammatory responses of these cells. Alterations in the membrane potential of activated neutrophils may play a role in regulating calcium reuptake into the cells as attenuation of the membrane depolarisation response is associated with accelerated calcium influx. Modulation of the activity of the endomembrane Ca(2+)-ATPase in human neutrophils represents an important target for anti-inflammatory