PRODUCTION OF 15-HYDROXYEICOSATETRAENOIC ACID BY PURIFIED HUMAN EOSINOPHILS AND NEUTROPHILS

被引:15
作者
MORITA, E [1 ]
SCHRODER, JM [1 ]
CHRISTOPHERS, E [1 ]
机构
[1] UNIV KIEL,DEPT DERMATOL,W-2300 KIEL 1,GERMANY
关键词
D O I
10.1111/j.1365-3083.1990.tb03190.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the presence of high concentrations of exogenous arachidonic acid (≥ 10 μm). eosinophils produced 15‐hydroxycicosatetraenoic acid (15‐HETE) in the absence of stimuli. The calcium ionophore A23187, as well as the chemotaxins used in this study‐complement split product C5a, platelet‐activating factor (PAF). and,N‐formyl‐methionyl‐leucyl‐phenylalanine(FMLP)–failed to increase 15‐HETE production, indicating that eosinophil 15‐lipoxygenase is already active Production of 15‐HETE from eosinophils increased with increasing concentrations of arachidonic acid, exogenously added. Maximal 15‐HETE production was observed to he 1111 ± 380 ng per 106 eosinophils at the concentration of 100μm of arachidonic acid. With low concentrations of exogenous arachidonic acid (below 2;μm). eosinophils were considered to incorporate exogenous arachidonic acid into their cell membrane, and did not produce 15‐HETE. In contrast, 15‐HETE formation in highly purified neutrophils (eosinophils < 1%) was negligible compared with that in eosinophils (.300‐fold less), suggesting that 15 f HETE‐forming activity in granulocytes is derived from the eosinophil 15‐lipoxygetiase pathway and that neutrophils may lack 15‐lipoxygcnase activity. Copyright © 1990, Wiley Blackwell. All rights reserved
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页码:497 / 502
页数:6
相关论文
共 24 条
[1]   NEW CONCEPTS IN THE MODULATION OF LEUKOTRIENE SYNTHESIS [J].
BORGEAT, P ;
DELACLOS, BF ;
MACLOUF, J .
BIOCHEMICAL PHARMACOLOGY, 1983, 32 (03) :381-387
[2]   ON THE OPTIMAL CONDITIONS OF LTC4 FORMATION BY HUMAN EOSINOPHILS INVITRO [J].
BRUYNZEEL, PLB ;
KOK, PTM ;
VIETOR, RJ ;
VERHAGEN, J .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1985, 20 (01) :11-22
[3]   INHIBITION OF HUMAN-LEUKOCYTE 5-LIPOXYGENASE BY 15-HPETE AND RELATED EICOSANOIDS [J].
CASHMAN, JR ;
LAMBERT, C ;
SIGAL, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 155 (01) :38-44
[4]  
GARTNER I, 1980, IMMUNOLOGY, V40, P133
[5]  
HENDERSON WR, 1984, IMMUNOLOGY, V51, P679
[6]   NOVEL LEUKOTRIENES - PRODUCTS FORMED BY INITIAL OXYGENATION OF ARACHIDONIC-ACID AT C-15 [J].
JUBIZ, W ;
RADMARK, O ;
LINDGREN, JA ;
MALMSTEN, C ;
SAMUELSSON, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 99 (03) :976-986
[7]  
LEVINE JD, 1986, P NATL ACAD SCI USA, V83, P5531
[8]   A 2ND PATHWAY OF LEUKOTRIENE BIOSYNTHESIS IN PORCINE LEUKOCYTES [J].
MAAS, RL ;
BRASH, AR ;
OATES, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09) :5523-5527
[9]  
MCGUIRE J, 1985, J BIOL CHEM, V260, P8316
[10]  
MORITA E, 1990, J IMMUNOL, V144, P1893