CHANGES IN NEUTROPHIL DEFORMABILITY FOLLOWING INVITRO SMOKE EXPOSURE - MECHANISM AND PROTECTION

被引:54
作者
DROST, EM [1 ]
SELBY, C [1 ]
LANNAN, S [1 ]
LOWE, GDO [1 ]
MACNEE, W [1 ]
机构
[1] GLASGOW ROYAL INFIRM,DEPT MED,GLASGOW G4 0SF,SCOTLAND
关键词
D O I
10.1165/ajrcmb/6.3.287
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
We have previously demonstrated a reduction in the deformability of neutrophils, exposed to whole particulate cigarette smoke in vitro, by measuring their ability to filter through a micropore membrane with pore dimensions similar to those of the average pulmonary capillary segment. In this study, we exposed neutrophils to the vapor phase of cigarette smoke and investigated the mechanism of the reduction in neutrophil filterability. Although both stimulated neutrophils and smoke-exposed neutrophils demonstrated an increase in filtration pressures, and thus a reduction in cell deformability, compared with control untreated cells, the spontaneous release of the reactive oxygen intermediates hydrogen peroxide and the superoxide anion was depressed following in vitro smoke exposure and there was no shape change to suggest that smoke-exposed cells were activated. The presence of erythrocytes, plasma, or the antioxidants albumin and glutathione prevented the reduction in cell filterability following smoke exposure, suggesting that in vitro smoke exposure, in our system, was mediated by oxidants. Indeed, the increase in filtration pressures, produced by smoke, could be mimicked by the addition of the oxidant hypochlorous acid. The cytoskeletal inhibitors cytochalasin B and D improved the filterability of smoke-exposed cells, suggesting that smoke may change neutrophil deformability through an effect on the actin component of the cytoskeleton. By contrast, colchicine, a specific inhibitor of the microtubules, had no effect. Preincubation with a monoclonal antibody to the CD18 antigen, to block this major neutrophil adhesive glycoprotein, did not alter the filtration pressure developed by stimulated or smoke-exposed neutrophils, suggesting that increased adhesivity was not the mechanism of the increase in filtration pressures observed following smoke exposure. Furthermore, we demonstrate that smoke-exposed neutrophils can recover their deformability in the presence of antioxidants. These data may help to explain the enhanced sequestration and subsequent emigration of neutrophils observed to occur in the lungs of smokers.
引用
收藏
页码:287 / 295
页数:9
相关论文
共 51 条
  • [1] ENDOTHELIAL AND EPITHELIAL-CELL ADHESION MOLECULES
    ALBELDA, SM
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 4 (03) : 195 - 203
  • [2] [Anonymous], 1965, ANESTHESIOLOGY
  • [3] AWASTHI YC, 1981, BLOOD, V58, P733
  • [4] BESWICK PH, 1986, J CLIN LAB IMMUNOL, V21, P71
  • [5] CYSTEINE AND GLUTATHIONE CONCENTRATIONS IN PLASMA AND BRONCHOALVEOLAR LAVAGE FLUID AFTER TREATMENT WITH N-ACETYLCYSTEINE
    BRIDGEMAN, MME
    MARSDEN, M
    MACNEE, W
    FLENLEY, DC
    RYLE, AP
    [J]. THORAX, 1991, 46 (01) : 39 - 42
  • [6] REDUCTION OF THE PROTEOLYTIC ACTIVITY OF NEUTROPHILS BY EXPOSURE TO CIGARETTE-SMOKE INVITRO
    BROWN, GM
    DROST, E
    DONALDSON, K
    MACGREGOR, I
    MACNEE, W
    [J]. EXPERIMENTAL LUNG RESEARCH, 1991, 17 (05) : 923 - 937
  • [7] OZONE AND HUMAN-BLOOD
    BUCKLEY, RD
    HACKNEY, JD
    CLARK, K
    POSIN, C
    [J]. ARCHIVES OF ENVIRONMENTAL HEALTH, 1975, 30 (01): : 40 - 43
  • [8] CALDER JH, 1963, LANCET, V1, P556
  • [9] NORMAL ALVEOLAR EPITHELIAL LINING FLUID CONTAINS HIGH-LEVELS OF GLUTATHIONE
    CANTIN, AM
    NORTH, SL
    HUBBARD, RC
    CRYSTAL, RG
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1987, 63 (01) : 152 - 157
  • [10] CHEIN S, 1984, WHITE CELL MECHANICS, P19