Inhibition of eosinophil rolling and recruitment in P-selectin- and intracellular adhesion molecule-1-deficient mice

被引:79
作者
Broide, DH
Humber, D
Sriramarao, P
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] La Jolla Inst Expt Med, Lab Immunol & Vasc Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1182/blood.V91.8.2847.2847_2847_2856
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine the relative in vivo importance of endothelial expressed adhesion molecules to eosinophil rolling, adhesion, and transmigration, we have induced eosinophilic peritonitis using ragweed allergen in P-selectin-deficient, intracellular adhesion molecule-1 (ICAM-1)-deficient and control wild-type mice, Circulating leukocytes visualized by intravital microscopy exhibited reduced rolling and firm adhesion in P-selectin-deficient mice and reduced firm adhesion in ICAM-1-deficient mice. Eosinophils exhibited reduced rolling and firm adhesion to endothelium in P-selectin-deficient mice. Eosinophil recruitment in P-selectin-deficient mice (similar to 75% inhibition of eosinophil recruitment) and ICAM-1-deficient mice (similar to 67% inhibition of eosinophil recruitment) was significantly reduced compared with wild-type mice. Eosinophil recruitment was not completely inhibited in P-selectin/ICAM-1 double-mutant mice (eosinophil recruitment inhibited similar to 62%). However, pretreatment of P-selectin/ICAM-1-deficient mice with an anti-vascular cell adhesion molecule (VCAM) antibody induced near complete inhibition of eosinophil recruitment, Overall, these studies show that eosinophil rolling and firm adhesion is significantly reduced in P-selectin-deficient mice and that P-selectin, ICAM-1, and VCAM are important to eosinophil peritoneal recruitment after ragweed challenge. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:2847 / 2856
页数:10
相关论文
共 38 条
[1]   E-SELECTIN SUPPORTS NEUTROPHIL ROLLING IN-VITRO UNDER CONDITIONS OF FLOW [J].
ABBASSI, O ;
KISHIMOTO, TK ;
MCINTIRE, LV ;
ANDERSON, DC ;
SMITH, CW .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2719-2730
[2]   THE INTEGRIN VLA-4 SUPPORTS TETHERING AND ROLLING IN FLOW ON VCAM-1 [J].
ALON, R ;
KASSNER, PD ;
CARR, MW ;
FINGER, EB ;
HEMLER, ME ;
SPRINGER, TA .
JOURNAL OF CELL BIOLOGY, 1995, 128 (06) :1243-1253
[3]   ALPHA-4 INTEGRINS MEDIATE LYMPHOCYTE ATTACHMENT AND ROLLING UNDER PHYSIOLOGICAL FLOW [J].
BERLIN, C ;
BARGATZE, RF ;
CAMPBELL, JJ ;
VONANDRIAN, UH ;
SZABO, MC ;
HASSLEN, SR ;
NELSON, RD ;
BERG, EL ;
ERLANDSEN, SL ;
BUTCHER, EC .
CELL, 1995, 80 (03) :413-422
[4]   ADHESION OF HUMAN BASOPHILS, EOSINOPHILS, AND NEUTROPHILS TO INTERLEUKIN 1-ACTIVATED HUMAN VASCULAR ENDOTHELIAL-CELLS - CONTRIBUTIONS OF ENDOTHELIAL-CELL ADHESION MOLECULES [J].
BOCHNER, BS ;
LUSCINSKAS, FW ;
GIMBRONE, MA ;
NEWMAN, W ;
STERBINSKY, SA ;
DERSEANTHONY, CP ;
KLUNK, D ;
SCHLEIMER, RP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (06) :1553-1556
[5]   Inhibition of pulmonary eosinophilia in P-selectin- and ICAM-1-deficient mice [J].
Broide, DH ;
Sullivan, S ;
Gifford, T ;
Sriramarao, P .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 18 (02) :218-225
[6]   P-SELECTIN ICAM-1 DOUBLE MUTANT MICE - ACUTE EMIGRATION OF NEUTROPHILS INTO THE PERITONEUM IS COMPLETELY ABSENT BUT IS NORMAL INTO PULMONARY ALVEOLI [J].
BULLARD, DC ;
QIN, L ;
LORENZO, I ;
QUINLIN, WM ;
DOYLE, NA ;
BOSSE, R ;
VESTWEBER, D ;
DOERSCHUK, CM ;
BEAUDET, AL .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1782-1788
[7]  
CARLOS TM, 1994, BLOOD, V84, P2068
[8]   EOSINOPHILIA IN TRANSGENIC MICE EXPRESSING INTERLEUKIN-5 [J].
DENT, LA ;
STRATH, M ;
MELLOR, AL ;
SANDERSON, CJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1425-1431
[9]   Eosinophil recruitment to the lung in a murine model of allergic inflammation - The role of T cells, chemokines, and adhesion receptors [J].
Gonzalo, JA ;
Lloyd, CM ;
Kremer, L ;
Finger, E ;
Martinez, C ;
Siegelman, MH ;
Cybulsky, M ;
GutierrezRamos, JC .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (10) :2332-2345
[10]   ANTIGEN-INDUCED RECRUITMENT OF EOSINOPHILS - IMPORTANCE OF CD4(+) T-CELLS, IL5, AND MAST-CELLS [J].
HOM, JT ;
ESTRIDGE, T .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1994, 73 (03) :305-311