IL-8 release and neutrophil activation by Clostridium difficile toxin-exposed human monocytes

被引:64
作者
Linevsky, JK
Pothoulakis, C
Keates, S
Warny, M
Keates, AC
Lamont, JT
Kelly, CP
机构
[1] Boston Univ, Med Ctr, Sch Med, Evans Mem Dept Clin Res, Boston, MA 02118 USA
[2] Dept Vet Affairs Med Ctr, Gastroenterol Sect, Boston, MA 02130 USA
[3] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02215 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1997年 / 273卷 / 06期
关键词
pseudomembranous colitis; intestinal inflammation; cytokines; adhesion molecules; interleukin-8;
D O I
10.1152/ajpgi.1997.273.6.G1333
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Neutrophil infiltration is central to the pathogenesis of Clostridium difficile toxin A-induced enterocolitis. This study examines whether monocyte activation by C. difficile toxins is instrumental in initiating neutrophil activation and recruitment. Human monocytes were exposed to low concentrations of highly purified C. difficile toxins, and the conditioned media were harvested for cytokine and functional assays. Monocytes exposed to C. difficile toxin A (10(-10) M) or toxin B (10(-12) M) released 100 and 20 times basal levels, respectively, of the neutrophil chemoattractant interleukin-8 (IL-8). Reverse trans criptase-polymerase chain reaction demonstrated a marked increase in IL-8 mRNA expression by monocytes 3 h after toxin exposure. Conditioned media from toxin A-and toxin B-treated monocytes stimulated neutrophil migration (324 and 245% of control, respectively). This effect was completely blocked by IL-8 antiserum. These media also upregulated neutrophil CD11b/CD18 and endothelial cell intercellular adhesion molecule-1 expression. C. difficile toxins, at low concentrations, potently activate monocytes to release factors, including IL-8, that facilitate neutrophil extravasation and tissue infiltration. Our findings indicate a major role for toxin-mediated monocyte and macrophage activation in C. difficile colitis.
引用
收藏
页码:G1333 / G1340
页数:8
相关论文
共 34 条
[21]   MACROPHAGE-DEPENDENT STIMULATION OF T-CELL-DEPLETED SPLEEN-CELLS BY CLOSTRIDIUM-DIFFICILE TOXIN-A AND CALCIUM IONOPHORE [J].
MILLER, PD ;
POTHOULAKIS, C ;
BAEKER, TR ;
LAMONT, JT ;
ROTHSTEIN, TL .
CELLULAR IMMUNOLOGY, 1990, 126 (01) :155-163
[22]   CLOSTRIDIUM-DIFFICILE TOXIN-A STIMULATES INTRACELLULAR CALCIUM RELEASE AND CHEMOTACTIC RESPONSE IN HUMAN-GRANULOCYTES [J].
POTHOULAKIS, C ;
SULLIVAN, R ;
MELNICK, DA ;
TRIADAFILOPOULOS, G ;
GADENNE, AS ;
MESHULAM, T ;
LAMONT, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) :1741-1745
[23]  
POTHOULAKIS C, 1986, J BIOL CHEM, V261, P1316
[24]   Pathogenesis of Clostridium difficile-associated diarrhoea [J].
Pothoulakis, C .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1996, 8 (11) :1041-1047
[25]   PSEUDOMEMBRANOUS COLITIS [J].
PRICE, AB ;
DAVIES, DR .
JOURNAL OF CLINICAL PATHOLOGY, 1977, 30 (01) :1-12
[26]   UPTAKE OF EXTRACELLULAR ENZYME BY A NOVEL PATHWAY IS A MAJOR DETERMINANT OF CATHEPSIN-L LEVELS IN HUMAN MACROPHAGES [J].
REILLY, JJ ;
CHEN, P ;
SAILOR, LZ ;
MASON, RW ;
CHAPMAN, HA .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :176-183
[27]   CLOSTRIDIUM-DIFFICILE TOXIN-B IS MORE POTENT THAN TOXIN-A IN DAMAGING HUMAN COLONIC EPITHELIUM IN-VITRO [J].
RIEGLER, M ;
SEDIVY, R ;
POTHOULAKIS, C ;
HAMILTON, G ;
ZACHERI, J ;
BISCHOF, G ;
COSENTINI, E ;
FEIL, W ;
SCHIESSEL, R ;
LAMONT, JT ;
WENZL, E .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2004-2011
[28]   EFFECTS OF CLOSTRIDIUM-DIFFICILE TOXIN-B ON HUMAN MONOCYTES AND MACROPHAGES - POSSIBLE RELATIONSHIP WITH CYTOSKELETAL REARRANGEMENT [J].
SIFFERT, JC ;
BALDACINI, O ;
KUHRY, JG ;
WACHSMANN, D ;
BENABDELMOUMENE, S ;
FARADJI, A ;
MONTEIL, H ;
POINDRON, P .
INFECTION AND IMMUNITY, 1993, 61 (03) :1082-1090
[29]   INTERLEUKIN-8 GENE-EXPRESSION BY A PULMONARY EPITHELIAL-CELL LINE - A MODEL FOR CYTOKINE NETWORKS IN THE LUNG [J].
STANDIFORD, TJ ;
KUNKEL, SL ;
BASHA, MA ;
CHENSUE, SW ;
LYNCH, JP ;
TOEWS, GB ;
WESTWICK, J ;
STRIETER, RM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (06) :1945-1953
[30]  
STRIETER RM, 1994, J LAB CLIN MED, V123, P183