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First published online 26 October 2004
doi: 10.1242/jcs.01498


Journal of Cell Science 117, 5749-5757 (2004)
Published by The Company of Biologists 2004
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Research Article

Platelet-activating factor stimulates cytoplasmic alkalinization and granule acidification in human eosinophils

Jennifer L. Bankers-Fulbright1, Gail M. Kephart1, Kathleen R. Bartemes1, Hirohito Kita1,2 and Scott M. O'Grady3,*

1 Department of Medicine, Mayo Clinic College of Medicine, Rochester, MN 55905, USA
2 Department of Immunology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA
3 Departments of Physiology and Animal Science, University of Minnesota, 1988 Fitch Avenue, St. Paul, MN 55108, USA

* Author for correspondence (e-mail: ograd001{at}umn.edu)

Accepted 17 August 2004

The effects of platelet-activating factor (PAF) and IL-5 on intracellular pH were investigated in human eosinophils. Purified peripheral blood eosinophils were loaded with the ratiometric fluorescent pH indicator BCECF-AM ester. Stimulation of eosinophils with PAF produced time-dependent alkalinization of the cytoplasm from an initial pH of 7.1±0.04 to 7.5±0.05. A similar alkalinization response was produced by the calcium ionophore, ionomycin and by the calcium ATPase inhibitor, thapsigargin. These compounds as well as PAF produce significant increases in cytoplasmic calcium ([Ca2+]i). In contrast, IL-5 and the protein kinase C (PKC) activator phorbol myristate acetate (PMA) did not produce cytoplasmic alkalinization and had no effect on [Ca2+]i in eosinophils. PAF-stimulated alkalinization was not inhibited under conditions that blocked plasma membrane Na+-H+ exchange, proton channel or plasma membrane H+-ATPase activities. Measurements of intragranule pH with a cell permeant pH indicator (LysoSensor Yellow/Blue DND-160), which partitions into intracellular acidic compartments, revealed that PAF-stimulated cytosolic alkalinization correlated with intragranule acidification. These results suggest that the increase in [Ca2+]i after PAF stimulation activates a H+-ATPase present in the granule membranes, leading to enhanced granule acidification and cytoplasmic alkalinization. We propose that granule acidification is an important step in solubilization of major basic protein crystals, which are stored within the granule core, in preparation for degranulation and release of these proteins.

Key words: Eosinophils, pH regulation, IL-5, PAF, H+-ATPase


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