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Research Article |
1 Division of Clinical Biochemistry, University of Geneva Medical School, 1211
Geneva 14, Switzerland
2 Division of Infectious Diseases, University Hospital Geneva, 1211 Geneva 14,
Switzerland
3 Immunology Laboratory, Faculty of Sciences, University Nancy 1, 54506
Vandoeuvre-les-Nancy, France
* Author for correspondence (e-mail: Sten_Theander{at}hotmail.com )
Accepted 6 May 2002
Ca2+-induced exocytosis in neuronal and neuroendocrine cells
involves ATP-dependent steps believed to `prime' vesicles for exocytosis.
Primed, docked vesicles are released in response to Ca2+ influx
through voltage-gated Ca2+ channels. Neutrophils, however, do not
possess voltage-gated Ca2+ channels and appear to have no docked
vesicles. Furthermore, neutrophils have several types of granules with
markedly different Ca2+ requirements for exocytosis. These
differential Ca2+ dependencies were used as a tool to investigate
the ATP dependence of different granule populations. Here we demonstrate
distinct ATP requirements for release of neutrophil granule populations, with
respect to rate as well as amplitude. Intracellular ATP was depleted to
various levels, and exocytosis was stimulated with different Ca2+
concentrations and measured with the patch-clamp capacitance technique or by
detecting enzyme release. Primary granule exocytosis displayed a distinct ATP
dependence with an apparent Km of
80 µM ATP and no
ATP-independent exocytosis. Release of secondary and tertiary granules
displayed a more shallow ATP dependence (Km
330 µM), and
more than 50% of secondary and tertiary granules appeared not to need ATP at
all for their release. Individual granules in human neutrophils have distinct
ATP requirements for exocytosis, suggesting that the ATP-sensitive elements
are localised to the granules. Primary granule exocytosis has a very low
affinity for ATP. Furthermore, substantial ATP-independent exocytosis of
secondary and tertiary granule occurs despite the absence of docked granules.
These characteristics should help neutrophils to fulfil their bactericidal
functions at poorly irrigated sites of infection with low glucose supply.
Key words: Exocytosis, ATP affinity, Granule populations, Ca2+, Neutrophils
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