Bronchial mast cells are the dominating LTC4S-expressing cells in aspirin-tolerant asthma

被引:41
作者
Cai, YQ
Bjermer, L
Halstensen, TS
机构
[1] Univ Oslo, Inst Oral Biol, N-0316 Oslo, Norway
[2] NTNU, Dept Circulat & Med Imaging, Fac Med, Trondheim, Norway
[3] Univ Trondheim Hosp, Dept Med, Dept Lung Med, N-7006 Trondheim, Norway
关键词
D O I
10.1165/rcmb.2002-0174OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The increased bronchial production of leukotriene C-4 (LTC4) in asthma is assumed to derive from infiltrating eosinophils expressing LTC4-synthase (LTC4S). Multicolor immunohistofluorescence examination of bronchial cryosections from 30 treated, untreated, or bronchial antigen-provoked aspirin-tolerant individuals with asthma and nine control subjects revealed that the dominating LTC4S-expressing cells were mast cells (> 80%), and not eosinophils. Whereas 95% of the mast cells expressed high levels of LTC4S, only 8-27% of the eosinophils expressed low levels. Image analysis revealed a significantly higher LTC4S expression levels in mast cells than in eosinophils. The bronchial mRNA levels for LTC4S did not correlate with the densities of LTC4S-positive eosinophils or mast cells. Treated individuals with asthma with more than 12% reversibility had significantly higher density of LTC4S-positive mast cells than those with less reversibility, and it correlated significantly with reduction in lung function (FEV1-predicted), both before and after salbutamol inhalation. Thus, mucosal mast cells, and not eosinophils, were the dominating LTC4S-containing cells in both untreated and treated aspirin-tolerant asthma. The density of LTC4S-positive mast cells correlated, moreover, with both the reduction in lung function and the degree of reversibility in treated asthma.
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收藏
页码:683 / 693
页数:11
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共 35 条
  • [1] Prednisolone treatment in asthma - Reduction in the numbers of eosinophils, T cells, tryptase-only positive mast cells, and modulation of IL-4, IL-5, and interferon-gamma cytokine gene expression within the bronchial mucosa
    Bentley, AM
    Hamid, Q
    Robinson, DS
    Schotman, E
    Meng, Q
    Assoufi, B
    Kay, AB
    Durham, SR
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (02) : 551 - 556
  • [2] Mast-cell responses in the development of asthma
    Bingham, CO
    Austen, KF
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (02) : S527 - S534
  • [3] BLEECKER ER, 1991, J ALLERGY CLIN IMMUN, V88, P808
  • [4] BOUABOULA M, 1992, J BIOL CHEM, V267, P21830
  • [5] Overexpression of leukotriene C4 synthase in bronchial biopsies from patients with aspirin-intolerant asthma
    Cowburn, AS
    Sladek, K
    Soja, J
    Adamek, L
    Nizankowska, E
    Szczeklik, A
    Lam, BK
    Penrose, JF
    Austen, KF
    Holgate, ST
    Sampson, AP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (04) : 834 - 846
  • [6] LEUKOTRIENES ARE POTENT CONSTRICTORS OF HUMAN BRONCHI
    DAHLEN, SE
    HEDQVIST, P
    HAMMARSTROM, S
    SAMUELSSON, B
    [J]. NATURE, 1980, 288 (5790) : 484 - 486
  • [7] DRAZEN JM, 1996, PULMONARY CRITICAL C, P143
  • [8] EFFECT OF ORAL PREDNISONE ON AIRWAY INFLAMMATORY MEDIATORS IN ATOPIC ASTHMA
    DWORSKI, R
    FITZGERALD, GA
    OATES, JA
    SHELLER, JR
    WORKMAN, R
    PRAKASH, C
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (04) : 953 - 959
  • [9] INTRAEPITHELIAL T-CELLS OF THE TCR-GAMMA/DELTA+CD8- AND V-DELTA-1/J-DELTA-1+ PHENOTYPES ARE INCREASED IN CELIAC-DISEASE
    HALSTENSEN, TS
    SCOTT, H
    BRANDTZAEG, P
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1989, 30 (06) : 665 - 672
  • [10] T helper cell type 2 cytokines coordinately regulate immunoglobulin E-dependent cysteinyl leukotriene production by human cord blood-derived mast cells:: Profound induction of leukotriene C4 synthase expression by interleukin 4
    Hsieh, FH
    Lam, BK
    Penrose, JF
    Austen, KF
    Boyce, JA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (01) : 123 - 133