ROLE OF RECRUITED NEUTROPHILS IN INTERLEUKIN-8 PRODUCTION IN DOG TRACHEA AFTER STIMULATION WITH PSEUDOMONAS IN-VIVO

被引:14
作者
INOUE, H
HARA, M
MASSION, PP
GRATTAN, KM
LAUSIER, JA
CHAN, B
KANEKO, T
ISONO, K
JORENS, PG
UEKI, IF
NADEL, JA
机构
[1] UNIV CALIF SAN FRANCISCO, CARDIOVASC RES INST, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT MED, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1165/ajrcmb.13.5.7576693
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
Cell-free supernatant of Pseudomonas aeruginosa (PA) recruits neutrophils into the airways indirectly by inducing the production of chemotactic factors, including interleukin-8 (IL-8). PA products stimulate IL-8 expression selectively in surface airway epithelium, gland ducts, serous cells, and recruited neutrophils. To examine the relative contribution of neutrophils in IL-8 release in the airway lumen, we studied the effect of inhibition of neutrophil recruitment on IL-8 concentration in tracheal fluid after introduction of PA supernatant into the dog trachea in vivo. Tracheal superfusion with PA supernatant caused neutrophil recruitment and increased the IL-8 concentration in the tracheal lumen; NPC 15669 inhibited both effects. To study whether migration of neutrophils into the airway lumen per se induces their expression of IL-8, we compared effects of local introduction of IL-8 and of PA supernatant into the trachea on IL-8 expression in neutrophils recruited into the trachea. PA supernatant, but not exogenous IL-8 alone, induced IL-8 mRNA expression in neutrophils recruited into the trachea. To determine what product(s) of PA stimulate IL-8 expression in neutrophils, we examined neutrophils isolated from peripheral blood. PA supernatant induced IL-8 production in neutrophils, an effect reproduced by PA lipopolysaccharide and inhibited by polymyxin B. These results suggest that neutrophils recruited into the airway lumen play a major role in local IL-8 production in airways in response to bacteria such as PA, depending on the presence of stimuli such as lipopolysaccharide.
引用
收藏
页码:570 / 577
页数:8
相关论文
共 29 条
[1]   N-[9H-(2,7-DIMETHYLFLUORENYL-9-METHOXY)CARBONYL]-L-LEUCINE, NPC-15669, PREVENTS NEUTROPHIL ADHERENCE TO ENDOTHELIUM AND INHIBITS CD11B/CD18 UP-REGULATION [J].
BATOR, JM ;
WEITZBERG, M ;
BURCH, RM .
IMMUNOPHARMACOLOGY, 1992, 23 (02) :139-149
[2]   PHAGOCYTOSING NEUTROPHILS PRODUCE AND RELEASE HIGH AMOUNTS OF THE NEUTROPHIL-ACTIVATING PEPTIDE-1/INTERLEUKIN-8 [J].
BAZZONI, F ;
CASSATELLA, MA ;
ROSSI, F ;
CESKA, M ;
DEWALD, B ;
BAGGIOLINI, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :771-774
[3]   EVIDENCE OF A ROLE FOR MESOTHELIAL CELL-DERIVED INTERLEUKIN-8 IN THE PATHOGENESIS OF ASBESTOS-INDUCED PLEURISY IN RABBITS [J].
BOYLAN, AM ;
RUEGG, C ;
KIM, KJ ;
HEBERT, CA ;
HOEFFEL, JM ;
PYTELA, R ;
SHEPPARD, D ;
GOLDSTEIN, IM ;
BROADDUS, VC .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (04) :1257-1267
[4]  
BURCH RM, 1993, J IMMUNOL, V150, P3397
[5]   N-(FLUORENYL-9-METHOXYCARBONYL) AMINO-ACIDS, A CLASS OF ANTIINFLAMMATORY AGENTS WITH A DIFFERENT MECHANISM OF ACTION [J].
BURCH, RM ;
WEITZBERG, M ;
BLOK, N ;
MUHLHAUSER, R ;
MARTIN, D ;
FARMER, SG ;
BATOR, JM ;
CONNOR, JR ;
KO, C ;
KUHN, W ;
MCMILLAN, BA ;
RAYNOR, M ;
SHEARER, BG ;
TIFFANY, C ;
WILKINS, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (02) :355-359
[6]   CFTR EXPRESSION AND CHLORIDE SECRETION IN POLARIZED IMMORTAL HUMAN BRONCHIAL EPITHELIAL-CELLS [J].
COZENS, AL ;
YEZZI, MJ ;
KUNZELMANN, K ;
OHRUI, T ;
CHIN, L ;
ENG, K ;
FINKBEINER, WE ;
WIDDICOMBE, JH ;
GRUENERT, DC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (01) :38-47
[7]   INTERLEUKIN-8 CONCENTRATIONS ARE ELEVATED IN BRONCHOALVEOLAR LAVAGE, SPUTUM, AND SERA OF CHILDREN WITH CYSTIC-FIBROSIS [J].
DEAN, TP ;
DAI, Y ;
SHUTE, JK ;
CHURCH, MK ;
WARNER, JO .
PEDIATRIC RESEARCH, 1993, 34 (02) :159-161
[8]  
ESTERLY JR, 1968, JOHNS HOPKINS MED J, V122, P94
[9]   REGULATION OF NEUTROPHIL INTERLEUKIN-8 GENE-EXPRESSION AND PROTEIN SECRETION BY LPS, TNF-ALPHA, AND IL-1-BETA [J].
FUJISHIMA, S ;
HOFFMAN, AR ;
VU, T ;
KIM, KJ ;
ZHENG, H ;
DANIEL, D ;
KIM, Y ;
WALLACE, EF ;
LARRICK, JW ;
RAFFIN, TA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 154 (03) :478-485
[10]  
HOIBY N, 1982, ACTA PAEDIATR SCAND, P33