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Modulation of the beta-adrenergic-response in cultured rat heart cells
Authors:Gerd Wallukat  Frank-D Boehmer  Ulla Engstroem  Peter Langen  Morley Hollenberg  Joachim Behlke  Hartmut Kuehn  Richard Grosse
Institution:(1) Centro de Investigaciones Biológicas, C. S. I. C., Velázquez 144, E-28006 Madrid, Spain;(2) Department of Biochemistry, Dartmouth Medical School, 03756 Hanover, New Hampshire, USA
Abstract:Summary Subcellular fractionation studies in resting human neutrophils indicated a bimodal distribution for cytochrome b. A. major peak of cytochrome b co-sedimented with gelatinase under different experimental conditions. This localization was partially overlapped with specific granules (using lysozyme and lactoferrin as specific granule markers), but clearly resolved from azurophilic granules, plasma membrane, mitochondria, as well as from a novel alkaline phosphatase-rich intracellular organelle. A minor localization of cytochrome b was found in fractions enriched in both the plasma membrane marker 5prime-nucleotidase and alkaline phosphatase. A significant portion of ubiquinone cell content co-fractionated with the gelatinase-containing granules. After phorbol myristate acetate (PMA)-cell stimulation, cytochrome b was mobilized to fractions showing respiratory burst activity and enriched in 5prime-nucleotidase activity. This mobilization paralleled secretion of gelatinase and lysozyme to the extracellular medium. Furthermore, neutrophil stimulation with fluoride in the absence of cytochalasin B induced release of gelatinase and generation of superoxide anion with only minimal release of lysozyme. Preincubation of cells with the anion channel blocker 4,4prime-diisothiocyanostilbene-2,2prime-disulfonic acid (DIDS) prevented lysozyme release, but had only a minor effect on the release of gelatinase and did not inhibit the superoxide anion generation elicited by N-formyl-methionyl-leucyl-phenylalanine or PMA. These results suggest a main location of cytochrome b in mobilizable gelatinase-containing granules, which can constitute a subpopulation of specific granules. Furthermore, these findings show that the gelatinase-containing granule is functionally involved in the respiratory burst in neutrophils and that membrane fusion between plasma membrane and the gelatinase-containing granule occurs during activation of cells.Abbreviations DIDS 4,4prime-diisothiocyanostilbene-2,2prime-disulfonic acid - FMLP N-formyl-methionyl-leucyl-phenylalanine - PMA 4beta-phorbol, 12-myristate, 13-acetate
Keywords:cytochrome b  gelatinase  cytoplasmic granules  membrane fusion  respiratory burst  human neutrophil
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