Reference : Interleukin-8 primes oxidative burst in neutrophil-like HL-60 through changes in cyto... |
Scientific journals : Article | |||
Life sciences : Biochemistry, biophysics & molecular biology | |||
http://hdl.handle.net/10993/5719 | |||
Interleukin-8 primes oxidative burst in neutrophil-like HL-60 through changes in cytosolic calcium | |
English | |
Bréchard, Sabrina ![]() | |
Bueb, Jean-Luc ![]() | |
Tschirhart, Eric ![]() | |
2005 | |
Cell Calcium | |
Churchill Livingstone, Inc. | |
37 | |
6 | |
531-40 | |
Yes (verified by ORBilu) | |
0143-4160 | |
Edinburgh | |
Scotland | |
[en] drug effects ; Fura-2 ; HL-60 Cells ; Humans ; Hydrogen Peroxide ; Interleukin-8 ; N-Formylmethionine Leucyl-Phenylalanine ; Neutrophils ; Oxazines ; Reactive Oxygen Species ; Respiratory Burst ; physiology ; metabolism ; pharmacology ; Calcium | |
[en] In response to a variety of stimuli, neutrophils release large amount of reactive oxygen species (ROS) generated by NADPH oxidase. This process known as the respiratory burst is dependent on cytosolic free calcium concentration ([Ca(2+)](i)). Proinflammatory cytokines such as interleukin-8 (IL-8) may modulate ROS generation through a priming phenomenon. The aim of this study was to determine the effect of human IL-8 on ROS production in neutrophil-like dimethylsulfoxide-differentiated HL-60 cells (not equalHL-60 cells) and further to examine the role of Ca(2+) mobilization during the priming. IL-8 at 10 nM induced no ROS production but a [Ca(2+)](i) rise (254 +/- 36 nM). IL-8 induced a strongly enhanced (2 fold) ROS release during stimulation with 1 microM of N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF). This potentiation of ROS production is dependent of extracellular Ca(2+) (17.0+/-4.5 arbitrary units (A.U.) in the absence of Ca(2+) versus 56.6 +/- 3.9 A.U. in the presence of 1.25 mM of Ca(2+)). Also, IL-8 enhanced fMLF-stimulated increase in [Ca(2+)](i) (375 +/- 35 versus 245 +/- 21 nM, 0.1 microM of fMLF). IL-8 had no effect on not equalHL-60 cells in response to 1 microM of thapsigargin (472 +/- 66 versus 470 +/- 60 nM). In conclusion, Ca(2+) influx is necessary for a full induction of neutrophil priming by IL-8. | |
http://hdl.handle.net/10993/5719 | |
10.1016/j.ceca.2005.01.019 |
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