N-formyl-methionyl-leucyl-phenylalanine induces and modulates IL-1 and IL-6 in human PBMC

被引:18
作者
Arbour, N [1 ]
Tremblay, P [1 ]
Oth, D [1 ]
机构
[1] UNIV QUEBEC,INST ARMAND FRAPPIER,CTR RECH IMMUNOL,LAVAL,PQ H7N 4Z3,CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
cytokines; N-formyl-methionyl-leucyl-phenylalanine; IL; 1; IL-6; PBMC;
D O I
10.1006/cyto.1996.0063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N-formyl-methionyl-leucyl-phenylalanine (fMLP), a bacterial derivative, induces and modulates various cellular responses linked to inflammation. In this work we evaluated the impact of fMLP stimulation on three pro-inflammatory cytokines: IL-1 alpha, IL-1 beta and IL-6, We found that MLP induces the secretion of IL-1 alpha, IL-1 beta and IL-6 in human peripheral blood mononuclear cells (PBMC), It also increased LPS-induced secretion of these three cytokines. Northern blot analysis demonstrated that fMLP induced IL-1 alpha, IL-1 beta and IL-6 gene expression by human PBMC, The fMLP-induced IL-1 alpha and IL-1 beta gene expression and IL-6 secretion were abolished by pertussis toxin pretreatment, which suggests that the fMLP induction of cytokine was also mediated via a G(i) protein, The concentration range of fMLP used to obtain these effects, in a dose dependent fashion, was 20 mu M to 1100 mu M. The mechanism by which fMLP modulates cytokine secretion is still not characterized, fMLP seems to share similar biological activities with other chemotactic factors (C5a, MCP-1, PAF, IL-8) that are able to modulate cytokines, and whose receptors belong to the same superfamily as the fMLP receptor(s). (C) 1996 Academic Press Limited
引用
收藏
页码:468 / 475
页数:8
相关论文
共 38 条
[31]   LIPOPOLYSACCHARIDES PRIME WHOLE HUMAN BLOOD AND ISOLATED NEUTROPHILS FOR THE INCREASED SYNTHESIS OF 5-LIPOXYGENASE PRODUCTS BY ENHANCING ARACHIDONIC-ACID AVAILABILITY - INVOLVEMENT OF THE CD14 ANTIGEN [J].
SURETTE, ME ;
PALMANTIER, R ;
GOSSELIN, J ;
BORGEAT, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) :1347-1355
[32]   DIFFERENTIAL-EFFECTS OF PKC INHIBITORS ON GELATINASE-B AND INTERLEUKIN-6 PRODUCTION IN THE MOUSE MACROPHAGE [J].
TREMBLAY, P ;
HOUDE, M ;
ARBOUR, N ;
ROCHEFORT, D ;
MASURE, S ;
MANDEVILLE, R ;
OPDENAKKER, G ;
OTH, D .
CYTOKINE, 1995, 7 (02) :130-136
[33]  
TREMBLAY P, 1991, IMMUNOL INFECT DIS, V1, P329
[34]  
TREMBLAY P, 1991, INT J CELL CLONING, V9, P385
[35]   CALCIUM INFLUX STIMULATES A 2ND PATHWAY FOR SUSTAINED DIACYLGLYCEROL PRODUCTION IN LEUKOCYTES ACTIVATED BY CHEMOATTRACTANTS [J].
TRUETT, AP ;
VERGHESE, MW ;
DILLON, SB ;
SNYDERMAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1549-1553
[36]   SPECIFIC RECEPTOR-SITES FOR CHEMOTACTIC PEPTIDES ON HUMAN POLYMORPHONUCLEAR LEUKOCYTES [J].
WILLIAMS, LT ;
SNYDERMAN, R ;
PIKE, MC ;
LEFKOWITZ, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (03) :1204-1208
[37]   ISOLATION OF A CDNA THAT ENCODES A NOVEL GRANULOCYTE N-FORMYL PEPTIDE RECEPTOR [J].
YE, RD ;
CAVANAGH, SL ;
QUEHENBERGER, O ;
PROSSNITZ, ER ;
COCHRANE, CG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 184 (02) :582-589
[38]   INTERLEUKIN-8 MODULATES INTERLEUKIN-1-BETA, INTERLEUKIN-6 AND TUMOR-NECROSIS-FACTOR-ALPHA RELEASE FROM NORMAL HUMAN MONONUCLEAR-CELLS [J].
YU, CL ;
SUN, KH ;
SHEI, SC ;
TSAI, CY ;
TSAI, ST ;
WANG, JC ;
LIAO, TS ;
LIN, WM ;
CHEN, HL ;
YU, HS ;
HAN, SH .
IMMUNOPHARMACOLOGY, 1994, 27 (03) :207-214