RESPECTIVE ROLE OF POLYMORPHONUCLEAR LEUKOCYTES AND THEIR INTEGRINS (CD-11/18) IN THE LOCAL OR SYSTEMIC TOXICITY OF LIPOPOLYSACCHARIDE

被引:26
作者
CHANG, HR
VESIN, C
GRAU, GE
POINTAIRE, P
ARSENIJEVIC, D
STRATH, M
PECHERE, JC
PIGUET, PF
机构
[1] UNIV GENEVA,CTR MED UNIV,DEPT PATHOL,CH-1211 GENEVA 4,SWITZERLAND
[2] UNIV GENEVA,DEPT GENET & MICROBIOL,CH-1211 GENEVA 4,SWITZERLAND
[3] NATL INST MED RES,DIV PARASITOL,LONDON NW7 1AA,ENGLAND
关键词
INTEGRINS; NEUTROPHILS; LIPOPOLYSACCHARIDE TOXICITY;
D O I
10.1002/jlb.53.6.636
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The role of neutrophils (PMNs) and leukocyte integrins was investigated in two models of lipopolysaccharide (LPS)-induced toxicity: the systemic lethality assay in D-galactosamine-sensitized mice and the local reaction elicited by intradermal injection of LPS and tumor necrosis factor (TNF) at 24-h intervals. In the local reaction, depletion of PMNs with an anti-PMN monoclonal antibody (mAb) and mAbs against CD-11a (or LFA1) and CD-11b (or CR3) completely prevented the hemorrhagic necrosis. Evaluation of histological sections and myeloperoxidase levels suggested different mechanism of protection because PMNs were abundant in anti-CD11- and absent in anti-PMN-treated mice. In the systemic assay, depletion of PMNs ensured 100% survival, whereas after administration of anti-CD-11a or b mAb, the percentages of survivors were 6 and 59%, respectively. One hour after LPS injection, the serum TNF-alpha level was higher in PMN-depleted mice than in controls. These studies provide evidence that neutrophils are essential for the expression of local or systemic LPS-induced injury, whereas the requirement for their leukocytic integrins is obvious only in the local reaction.
引用
收藏
页码:636 / 639
页数:4
相关论文
共 23 条
[11]   ENDOTOXINS AND DISEASE MECHANISMS [J].
MORRISON, DC ;
RYAN, JL .
ANNUAL REVIEW OF MEDICINE, 1987, 38 :417-432
[12]  
MOVAT HZ, 1987, AM J PATHOL, V129, P463
[13]   TUMOR-NECROSIS-FACTOR AND CD11/CD18 (BETA-2) INTEGRINS ACT SYNERGISTICALLY TO LOWER CAMP IN HUMAN NEUTROPHILS [J].
NATHAN, C ;
SANCHEZ, E .
JOURNAL OF CELL BIOLOGY, 1990, 111 (05) :2171-2181
[14]   INHIBITION OF MURINE T-CELL-MEDIATED CYTOLYSIS AND T-CELL PROLIFERATION BY A RAT MONOCLONAL-ANTIBODY IMMUNOPRECIPITATING 2 LYMPHOID-CELL SURFACE POLYPEPTIDES OF 94000 AND 180000 MOLECULAR-WEIGHT [J].
PIERRES, M ;
GORIDIS, C ;
GOLSTEIN, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1982, 12 (01) :60-69
[15]   SHEDDING OF TUMOR-NECROSIS-FACTOR RECEPTORS BY ACTIVATED HUMAN NEUTROPHILS [J].
PORTEU, F ;
NATHAN, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (02) :599-607
[16]  
REMICK DG, 1990, AM J PATHOL, V136, P49
[17]   ANTIBODY TO THE MURINE TYPE-3 COMPLEMENT RECEPTOR INHIBITS LYMPHOCYTE-T-DEPENDENT RECRUITMENT OF MYELOMONOCYTIC CELLS INVIVO [J].
ROSEN, H ;
MILON, G ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (02) :535-548
[18]   SYNERGY BETWEEN TUMOR NECROSIS FACTOR AND BACTERIAL PRODUCTS CAUSES HEMORRHAGIC NECROSIS AND LETHAL SHOCK IN NORMAL MICE [J].
ROTHSTEIN, JL ;
SCHREIBER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (02) :607-611
[19]   CYTOKINE-ASSOCIATED TISSUE-INJURY AND LETHALITY IN MICE - A COMPARATIVE-STUDY [J].
SHALABY, MR ;
HALGUNSET, J ;
HAUGEN, OA ;
AARSET, H ;
AARDEN, L ;
WAAGE, A ;
MATSUSHIMA, K ;
KVITHYLL, H ;
BORASCHI, D ;
LAMVIK, J ;
ESPEVIK, T .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1991, 61 (01) :69-82
[20]  
SHEEHAN KCF, 1989, J IMMUNOL, V142, P3884