Release of adenosine from human neutrophils stimulated by platelet activating factor, leukotriene B4 and opsonized zymosan
Author(s) -
Sándor Sipka,
Zoltán Dinya,
M. Koltai,
P. Braquet,
G Szegedi
Publication year - 1992
Publication title -
mediators of inflammation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.37
H-Index - 97
eISSN - 1466-1861
pISSN - 0962-9351
DOI - 10.1155/s0962935192000413
Subject(s) - adenosine , zymosan , platelet activating factor , adenosine receptor , leukotriene b4 , chemistry , opsonin , phagocyte , phagocytosis , receptor , microbiology and biotechnology , biology , biochemistry , endocrinology , immunology , agonist , inflammation , in vitro
Isolated human polymorphonuclear leukocytes (PMNL) stimulated by platelet activating factor (PAF), leukotriene B(4) (LTB(4)) or opsonized zymosan (OZ) released adenosine measured by thermospray high performance liquid chromatography mass spectrometry in the cell-free supernatants. Stimulation by PAF or LTB(4) resulted in a bellshaped concentration-effect curve; 5 x 10(-7) M PAF, 10(-8) M LTB(4) and 500 mug ml(-1) OZ induced peak adenosine release, thus cytotoxic concentrations did not elevate adenosine level in the supernatants. Therefore adenosine release was characteristic of viable cells. As calculated from concentration-effect curves, the rank order of potency for adenosine release was PAF > LTB > OZ. These resuits suggest that adenosine, when bound specifically to membrane receptor sites, may initiate signal transduction, and, in co-operation with other inflammatory mediators, may modulate phagocyte function, e.g. production of chemoluminescence (CL).
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