Expression of intercellular adhesion molecule-1 in mice with Pseudomonas-induced pyelonephritis

被引:7
作者
Yokoo, A [1 ]
Hirose, T [1 ]
Matsukawa, M [1 ]
Hotta, H [1 ]
Kunishima, Y [1 ]
Takahashi, S [1 ]
机构
[1] Sapporo Med Univ, Sch Med, Dept Urol, Chuo Ku, Sapporo, Hokkaido 060, Japan
关键词
intercellular adhesion molecule-1; experimental pyelonephritis;
D O I
10.1016/S0022-5347(01)62964-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To investigate the role of intercellular adhesion molecule-1 (ICAM-1) in the renal inflammatory process, we studied the time-course fluctuation of ICAM-1 expression on inflammatory lesions in mice with experimentally induced bacterial pyelonephritis and the effect of in vivo administration of an anti-ICAM-1 monoclonal antibody (mAb) on leukocytic migration. Materials and Methods: Ascending pyelonephritis was induced by transurethral instillation of Pseudomonas aeruginosa, and the expression of ICAM-1 in the pyelonephritic lesions was studied by immunohistochemical methods. Results: The expression of ICAM-1 on the pyelonephritic lesions closely paralleled the degree of infiltration of neutrophils and macrophages until 3 days after infection. At 7 days after infection, though the degree of infiltration of these cells was quite high, expression of ICAM-1 was reduced. Treatment with the anti-ICAM-1 mAb in mice with bacterial pyelonephritis resulted in suppression of influx of neutrophils and macrophages in the infected sites until 3 days after infection. However, at 7 days after infection inhibition of the influx of these cells was not seen. Conclusions: These results suggest that ICAM-1 expression is transient and plays a key role in the influx of neutrophils and macrophages associated with the early-phase response, and that in the late phase ICAM-1 independent adhesion molecules may be more predominant.
引用
收藏
页码:592 / 596
页数:5
相关论文
共 23 条
[1]   THE SEVERE AND MODERATE PHENOTYPES OF HERITABLE MAC-1, LFA-1 DEFICIENCY - THEIR QUANTITATIVE DEFINITION AND RELATION TO LEUKOCYTE DYSFUNCTION AND CLINICAL-FEATURES [J].
ANDERSON, DC ;
SCHMALSTEIG, FC ;
FINEGOLD, MJ ;
HUGHES, BJ ;
ROTHLEIN, R ;
MILLER, LJ ;
KOHL, S ;
TOSI, MF ;
JACOBS, RL ;
WALDROP, TC ;
GOLDMAN, AS ;
SHEARER, WT ;
SPRINGER, TA .
JOURNAL OF INFECTIOUS DISEASES, 1985, 152 (04) :668-689
[2]  
[Anonymous], 1994, HDB MUCOSAL IMMUNOLO
[3]  
CARLOS TM, 1990, IMMUNOL REV, V114, P6
[4]  
COSIMI AB, 1990, J IMMUNOL, V144, P4604
[5]   ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE-1 MEDIATES ANTIGEN-INDUCED ACUTE AIRWAY INFLAMMATION AND LATE-PHASE AIRWAY-OBSTRUCTION IN MONKEYS [J].
GUNDEL, RH ;
WEGNER, CD ;
TORCELLINI, CA ;
CLARKE, CC ;
HAYNES, N ;
ROTHLEIN, R ;
SMITH, CW ;
LETTS, LG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (04) :1407-1411
[6]   UROEPITHELIAL CELLS ARE PART OF A MUCOSAL CYTOKINE NETWORK [J].
HEDGES, S ;
AGACE, W ;
SVENSSON, M ;
SJOGREN, AC ;
CESKA, M ;
SVANBORG, C .
INFECTION AND IMMUNITY, 1994, 62 (06) :2315-2321
[7]  
HINES RO, 1987, CELL, V48, P549
[8]  
HIROSE T, 1989, UROL RES, V17, P125
[10]   Intestinal epithelial cells: An integral component of the mucosal immune system [J].
Kagnoff, MF ;
Eckmann, L ;
Yang, SK ;
Huang, G ;
Jung, HC ;
Reed, SL ;
Fierer, J .
ESSENTIALS OF MUCOSAL IMMUNOLOGY, 1996, :63-71