Enhancement of normal neutrophil chemiluminescence by chronic granulomatous disease neutrophils
- 1 December 1989
- journal article
- research article
- Published by Springer Nature in Inflammation
- Vol. 13 (6) , 631-640
- https://doi.org/10.1007/bf00914307
Abstract
Neutrophils and other phagocytic cells from patients with chronic granulomatous disease (CGD) lack the ability to generate reactive oxygen intermediates (ROI), although other phagocytic functions appear to be intact. The effects of CGD neutrophils on the ability of normal neutrophils to produce ROI as measured by luminol-enhanced chemiluminescence (CL) were examined. Normal neutrophils (2×105) had a peak CL response to phorbol myristate acetate (PMA; 20 ng/ml) of 6.5±0.9 mV, while the CL response of CGD neutrophils was completely absent. However, the addition of CGD neutrophils (8×105) to normal neutrophils (2×105) markedly increased the peak CL response to PMA to 11.0+-1.1 mV (P < 0.001). The peak response of normal neutrophils (2×105) alone to the peptideN-formyl-methionyl-leucyl-phenylalanine (FMLP; 10−6 M) was 9.0±1.1mV, and this increased to 22.2±3.5 mV (P < 0.001) when 8×105 CGD neutrophils were added and to 18.9±3.6 mV (P5 CGD neutrophils were added. Thus, CGD neutrophils increase the release of ROI from normal cells, suggesting nonoxidative regulatory factors in ROI production.This publication has 31 references indexed in Scilit:
- COMPARISON BETWEEN LUMINOL- AND LUCIGENINDEPENDENT CHEMILUMINESCENCE OF POLYMORPHONUCLEAR LEUKOCYTESActa Pathologica Microbiologica Scandinavica Series C: Immunology, 2009
- Corticosteroids in treatment of obstructive lesions of chronic granulomatous diseaseThe Journal of Pediatrics, 1987
- Lucigenin chemiluminescence in the assessment of neutrophil superoxide productionJournal of Immunological Methods, 1987
- Radiological Case of the MonthArchives of Pediatrics & Adolescent Medicine, 1986
- Gastric Outlet Obstruction in Chronic Granulomatous Disease of ChildhoodArchives of Pediatrics & Adolescent Medicine, 1986
- Oxidative degradation of leukotriene C4 by human monocytes and monocyte-derived macrophages.The Journal of Experimental Medicine, 1985
- Chronic Granulomatous DiseaseMedicine, 1983
- Chronic Granulomatous Disease Involving the Central Nervous SystemPediatric Pathology, 1983
- Leukotriene B4, C4, D4 and E4 inactivation by hydroxyl radicalsBiochemical and Biophysical Research Communications, 1983
- Degranulation, membrane addition, and shape change during chemotactic factor-induced aggregation of human neutrophils.The Journal of cell biology, 1982