INCREASED EOSINOPHIL OXIDATIVE-METABOLISM BY TREATMENT WITH SOLUBLE INTERCELLULAR-ADHESION MOLECULE-1

被引:19
作者
CHIHARA, J
KAKAZU, T
HIGASHIMOTO, I
YAMAMOTO, T
KURACHI, D
NAKAJIMA, S
机构
[1] Fourth Department of Internal Medicine, Kinki University School of Medicine, Osaka
关键词
EOSINOPHILS; INTERCELLULAR ADHESION MOLECULE-1; BETA(2)-INTEGRIN; RADICAL OXYGEN PRODUCTS; CHEMILUMINESCENCE;
D O I
10.1159/000237201
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Adhesion molecules may play an important role not only in adherence of inflammatory cells (particularly eosinophils) to an inflamed focus but also in activation of these cells. It is therefore of interest to evaluate eosinophil activation via intercellular adhesion molecule-1 (ICAM-1) and the beta(2)-integrin family, namely CR3 (Mac-1), lymphocyte function-associated antigen (LFA)-1 alpha and LFA-1 beta, which are ligands for ICAM-1. Reactive oxygen species generated by eosinophils have also been considered capable of causing airway injury at the inflamed focus. This study examined the effect of recombinant soluble ICAM-1 and its ligands on eosinophil-induced radical oxygen products in terms of luminol-dependent chemiluminescence. Recombinant soluble ICAM-1 augmented eosinophil oxidative metabolism. It was concluded that signaling via adhesion molecules might play an important role in the pathogenesis of allergic inflammation through activation of eosinophils, e.g. an increase in oxidative metabolism.
引用
收藏
页码:45 / 47
页数:3
相关论文
共 12 条
  • [1] EOSINOPHILIC INFLAMMATION IN ASTHMA
    BOUSQUET, J
    CHANEZ, P
    LACOSTE, JY
    BARNEON, G
    GHAVANIAN, N
    ENANDER, I
    VENGE, P
    AHLSTEDT, S
    SIMONYLAFONTAINE, J
    GODARD, P
    MICHEL, FB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) : 1033 - 1039
  • [2] CAPRON M, 1989, PROGRESS IN ALLERGY AND CLINICAL IMMUNOLOGY, P6
  • [3] RANTES AUGMENTS RADICAL OXYGEN PRODUCTS FROM EOSINOPHILS
    CHIHARA, J
    HAYASHI, N
    KAKAZU, T
    YAMAMOTO, T
    KURACHI, D
    NAKAJIMA, S
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1994, 104 : 52 - 53
  • [4] A COMPARATIVE-STUDY OF EOSINOPHIL ISOLATION BY DIFFERENT PROCEDURES OF CD16-NEGATIVE DEPLETION
    CHIHARA, J
    KURACHI, D
    YAMAMOTO, T
    YAMADA, H
    WADA, T
    YASUKAWA, A
    NAKAJIMA, S
    [J]. ALLERGY, 1995, 50 (01) : 11 - 14
  • [5] HUMORAL AND CELLULAR STUDIES OF EOSINOPHILS IN REACTIVE AND MYELOPROLIFERATIVE SYNDROMES WITH MARKED EOSINOPHILIA
    CROWLEY, JP
    MYERS, TJ
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1983, 79 (03) : 301 - 305
  • [6] GLEICH GJ, 1986, ADV IMMUNOL, V39, P177
  • [7] PURIFICATION OF HUMAN-BLOOD EOSINOPHILS BY NEGATIVE SELECTION USING IMMUNOMAGNETIC BEADS
    HANSEL, TT
    POUND, JD
    PILLING, D
    KITAS, GD
    SALMON, M
    GENTLE, TA
    LEE, SS
    THOMPSON, RA
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 122 (01) : 97 - 103
  • [8] EOSINOPHILS IN IMMUNOLOGICAL REACTIONS - REPORT OF A WORKSHOP HELD AT THE 6TH-INTERNATIONAL-CONGRESS-OF-IMMUNOLOGY, TORONTO, CANADA, 10 JULY 1986
    KAY, AB
    [J]. CLINICAL ALLERGY, 1987, 17 (03): : 251 - 258
  • [9] ENHANCED EOSINOPHIL LUMINOL-DEPENDENT CHEMILUMINESCENCE IN ALLERGIC RHINITIS
    SHULT, PA
    GRAZIANO, FM
    BUSSE, WW
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1986, 77 (05) : 702 - 708
  • [10] Spry CJF, 1988, COMPREHENSIVE REV GU