A morphometric study of mucins and small airway plugging in cystic fibrosis

被引:115
作者
Burgel, Pierre-Regis
Montani, David
Danel, Claire
Dusser, Daniel J.
Nadel, Jay A.
机构
[1] Univ Paris 05, AP HP, Hop Cochin, Serv Pneumol, F-75679 Paris 14, France
[2] Univ Paris 05, AP HP, Hop Cochin, Serv Pneumol,UPRES EA 2511, F-75679 Paris 14, France
[3] Hop Europeen Georges Pompidou, AP HP, Anat Pathol Lab, Paris, France
[4] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[6] Univ Calif San Francisco, Dept Physiol, San Francisco, CA USA
关键词
D O I
10.1136/thx.2006.062190
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale: Little knowledge exists on structural changes and plugging in small airways in cystic fibrosis. Objective: To characterise the extent of plugging and contribution of secreted mucins to the plugs. Methods: Small airways in patients with cystic fibrosis at transplantation ( n = 18) were compared with control non- smokers ( n = 10). Tissue sections were stained with Alcian blue ( AB)/ periodicacid- Schiff ( PAS), for mucins MUC5B and MUC5AC, and for neutrophils and its chemoattractant interleukin ( IL) 8. Epidermal growth factor receptor ( EGFR) and its ligand pro- transforming growth factor a were also identified using immunohistochemical staining. Epithelial and luminal contents were assessed morphometrically. Results: Plugs occupying.50% of total luminal volume were found in 147 of 231 ( 63.6%) airways in patients with cystic fibrosis, but only in 1 of 39 ( 2.6%) airways in controls. In the epithelium of patients with cystic fibrosis, AB/ PAS, MUC5B, and MUC5AC- stained volume densities were increased 10- fold ( p, 0.01), indicating increased mucin production. In airway lumens, staining for mucins was also increased in cystic fibrosis, indicating increased mucin secretion. In the epithelium of patients with cystic fibrosis, neutrophil numbers were markedly increased and were inversely correlated with volume densities of mucous glycoconjugates ( r = 20.66, p, 0.005). IL8 staining was increased in the epithelium of patients with cystic fibrosis and colocalised with mucins. Staining for EGFR and for pro- transforming growth factor a were increased in the epithelium of patients with cystic fibrosis; positive correlations were found between EGFRstained volume density and both AB/ PAS and IL8- stained volume densities. Conclusions: Most of the small airways are plugged in cystic fibrosis at the time of transplantation. Mucins contribute to airway plugging. Recruited neutrophils may be involved in mucin secretion in the plugs. Increased expression of EGFR and its ligand suggests roles in mucin synthesis and neutrophil recruitment.
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页码:153 / 161
页数:9
相关论文
共 31 条
  • [1] Goblet cell degranulation after antigen challenge in sensitized guinea pigs - Role of neutrophils
    Agusti, C
    Takeyama, K
    Cardell, LO
    Ueki, I
    Lausier, J
    Lou, YP
    Nadel, JA
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (04) : 1253 - 1258
  • [2] Roles of epidermal growth factor receptor activation in epithelial cell repair and mucin production in airway epithelium
    Burgel, PR
    Nadel, JA
    [J]. THORAX, 2004, 59 (11) : 992 - 996
  • [3] Intranasal steroids decrease eosinophils but not mucin expression in nasal polyps
    Burgel, PR
    Cardell, LO
    Ueki, IF
    Nadel, JA
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2004, 24 (04) : 594 - 600
  • [4] Characterization of human mucin 5B gene expression in airway epithelium and the genomic clone of the amino-terminal and 5′-flanking region
    Chen, Y
    Zhao, YH
    Di, YP
    Wu, R
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 25 (05) : 542 - 553
  • [5] Conese Massimo, 2003, J Cyst Fibros, V2, P129, DOI 10.1016/S1569-1993(03)00063-8
  • [6] Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions
    Davies, JR
    Svitacheva, N
    Lannefors, L
    Kornfält, R
    Carlstedt, I
    [J]. BIOCHEMICAL JOURNAL, 1999, 344 : 321 - 330
  • [7] Mucin gene (MUC 2 and MUC 5AC) upregulation by Gram-positive and Gram-negative bacteria
    Dohrman, A
    Miyata, S
    Gallup, M
    Li, JD
    Chapelin, C
    Coste, A
    Escudier, E
    Nadel, J
    Basbaum, C
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1998, 1406 (03): : 251 - 259
  • [8] Pathophysiology and management of pulmonary infections in cystic fibrosis
    Gibson, RL
    Burns, JL
    Ramsey, BW
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) : 918 - 951
  • [9] Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung
    Groneberg, DA
    Eynott, PR
    Oates, T
    Lim, S
    Wu, R
    Carlstedt, I
    Nicholson, AG
    Chung, KF
    [J]. RESPIRATORY MEDICINE, 2002, 96 (02) : 81 - 86
  • [10] Immunolocalization of transforming growth factor α and epidermal growth factor receptor in lungs of patients with cystic fibrosis
    Hardie, WD
    Bejarano, PA
    Miller, MA
    Yankaskas, JR
    Ritter, JH
    Whitsett, JA
    Korfhagen, TR
    [J]. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 1999, 2 (05) : 415 - 423