Circulating Polymorphonuclear Leukocytes from Patients with Gram-Negative Bacteremia Are Not Primed for Enhanced Production of Leukotriene B4 or 5-Hydroxyeicosatetraenoic Acid
The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL....
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Published in | The Journal of infectious diseases Vol. 169; no. 5; pp. 1151 - 1154 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.05.1994
University of Chicago Press |
Subjects | |
Online Access | Get full text |
ISSN | 0022-1899 1537-6613 |
DOI | 10.1093/infdis/169.5.1151 |
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Abstract | The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL. PMNL from 11 bacteremic patients and 8 healthy subjects (11 samples) produced similar quantities of LTB4, ω-oxidation products of LTB4 , and 5-HETE after incubation with 0.3 and 0.5 µM A23187 for 5 min. At the detection threshold of 0.3 µM A23187, LTB4 was present in PMNL preparations from 9 of 11 patients and 7 of 11 control samples and 5-HETE from the same 9 patients and from 6 controls. There was no correlation between LTB4 or 5-HETE and plasma levels of endotoxin. In this group of patients, priming of PMNL by gram-negative bacteremia did not lead to enhanced production of LTB4 , its ω-oxidation products, or 5-HETE when PMNL were challenged with low concentrations of A23187. |
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AbstractList | The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL. PMNL from 11 bacteremic patients and 8 healthy subjects (11 samples) produced similar quantities of LTB4, ω-oxidation products of LTB4 , and 5-HETE after incubation with 0.3 and 0.5 µM A23187 for 5 min. At the detection threshold of 0.3 µM A23187, LTB4 was present in PMNL preparations from 9 of 11 patients and 7 of 11 control samples and 5-HETE from the same 9 patients and from 6 controls. There was no correlation between LTB4 or 5-HETE and plasma levels of endotoxin. In this group of patients, priming of PMNL by gram-negative bacteremia did not lead to enhanced production of LTB4 , its ω-oxidation products, or 5-HETE when PMNL were challenged with low concentrations of A23187. The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL. PMNL from 11 bacteremic patients and 8 healthy subjects (11 samples) produced similar quantities of LTB4, omega-oxidation products of LTB4, and 5-HETE after incubation with 0.3 and 0.5 microM A23187 for 5 min. At the detection threshold of 0.3 microM A23187, LTB4 was present in PMNL preparations from 9 of 11 patients and 7 of 11 control samples and 5-HETE from the same 9 patients and from 6 controls. There was no correlation between LTB4 or 5-HETE and plasma levels of endotoxin. In this group of patients, priming of PMNL by gram-negative bacteremia did not lead to enhanced production of LTB4, its omega-oxidation products, or 5-HETE when PMNL were challenged with low concentrations of A23187.The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL. PMNL from 11 bacteremic patients and 8 healthy subjects (11 samples) produced similar quantities of LTB4, omega-oxidation products of LTB4, and 5-HETE after incubation with 0.3 and 0.5 microM A23187 for 5 min. At the detection threshold of 0.3 microM A23187, LTB4 was present in PMNL preparations from 9 of 11 patients and 7 of 11 control samples and 5-HETE from the same 9 patients and from 6 controls. There was no correlation between LTB4 or 5-HETE and plasma levels of endotoxin. In this group of patients, priming of PMNL by gram-negative bacteremia did not lead to enhanced production of LTB4, its omega-oxidation products, or 5-HETE when PMNL were challenged with low concentrations of A23187. The hypothesis was tested that polymorphonuclear leukocytes (PMNL) from patients with gram-negative bacteremia are primed to produce leukotriene B4 (LTB4) or 5-hydroxyeicosatetraenoic acid (5-HETE), in response to concentrations of calcium ionophore A23187, which are substimulatory for control PMNL. PMNL from 11 bacteremic patients and 8 healthy subjects (11 samples) produced similar quantities of LTB4, omega-oxidation products of LTB4, and 5-HETE after incubation with 0.3 and 0.5 microM A23187 for 5 min. At the detection threshold of 0.3 microM A23187, LTB4 was present in PMNL preparations from 9 of 11 patients and 7 of 11 control samples and 5-HETE from the same 9 patients and from 6 controls. There was no correlation between LTB4 or 5-HETE and plasma levels of endotoxin. In this group of patients, priming of PMNL by gram-negative bacteremia did not lead to enhanced production of LTB4, its omega-oxidation products, or 5-HETE when PMNL were challenged with low concentrations of A23187. |
Author | Sorrell, Tania C. May, George L. Sztelma, Krystyna |
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Keywords | Human Leukocyte Pathogenesis In vitro Bacteremia Blood HETE Infection Calcium ion Leukotriene B4 Production Bacteriosis Microorganism culture Sensitization Ionophore Neutrophil Gram negative bacteria |
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Notes | Reprints or correspondence: Prof. T. C. Sorrell, Centre for Infectious Diseases and Microbiology, Westmead Hospital, Westmead, NSW 2145, Australia. ark:/67375/HXZ-TX7B8DCM-3 istex:EC50616EEB6F5834C93B8A7A0AB9BF3F2AA82ACF ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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SubjectTerms | Adult Aged Aged, 80 and over Bacteremia - immunology Bacterial diseases Bacterial sepsis Biological and medical sciences Calcimycin - pharmacology Endotoxins - pharmacology Female Gram-Negative Bacterial Infections - immunology Human bacterial diseases Humans Hydroxyeicosatetraenoic Acids - biosynthesis Infectious diseases Leukotriene B4 - biosynthesis Male Medical sciences Middle Aged Neutrophils - metabolism |
Title | Circulating Polymorphonuclear Leukocytes from Patients with Gram-Negative Bacteremia Are Not Primed for Enhanced Production of Leukotriene B4 or 5-Hydroxyeicosatetraenoic Acid |
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