Literature DB >> 1569186

Neutrophil elastase in respiratory epithelial lining fluid of individuals with cystic fibrosis induces interleukin-8 gene expression in a human bronchial epithelial cell line.

H Nakamura1, K Yoshimura, N G McElvaney, R G Crystal.   

Abstract

The respiratory manifestations of cystic fibrosis (CF) are characterized by neutrophil-dominated airway inflammation. Since a variety of inflammatory stimuli are capable of inducing bronchial epithelial cells to express the gene for IL-8, a cytokine that attracts and activates neutrophils, mediators in respiratory epithelial lining fluid (ELF) of CF individuals might induce IL-8 production by epithelial cells, thus recruiting neutrophils to the airways. BET-1A human bronchial epithelial cells at rest or incubated with normal ELF showed little IL-8 gene expression, but after incubation with CF ELF, a marked increase in IL-8 transcript levels was observed. CF ELF contained high levels of neutrophil elastase (NE) and various serine protease inhibitors prevented CF ELF from inducing IL-8 gene expression in BET-1A cells, suggesting that NE was the dominant inducer for IL-8 production in CF ELF. The addition of purified NE caused BET-1A cells to increase IL-8 gene transcription with accumulation of mRNA transcripts and to release IL-8-like neutrophil chemotactic activity. These observations suggest a self-perpetuating inflammatory process on the CF bronchial surface where NE released by neutrophils induced the bronchial epithelium to secrete IL-8, which in turn recruits additional neutrophils to the bronchial surface.

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Year:  1992        PMID: 1569186      PMCID: PMC443018          DOI: 10.1172/JCI115738

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  50 in total

1.  Down-regulation of cystic fibrosis gene mRNA transcript levels and induction of the cystic fibrosis chloride secretory phenotype in epithelial cells by phorbol ester.

Authors:  B C Trapnell; P L Zeitlin; C S Chu; K Yoshimura; H Nakamura; W B Guggino; J Bargon; T C Banks; W Dalemans; A Pavirani
Journal:  J Biol Chem       Date:  1991-06-05       Impact factor: 5.157

2.  The cystic fibrosis gene has a "housekeeping"-type promoter and is expressed at low levels in cells of epithelial origin.

Authors:  K Yoshimura; H Nakamura; B C Trapnell; W Dalemans; A Pavirani; J P Lecocq; R G Crystal
Journal:  J Biol Chem       Date:  1991-05-15       Impact factor: 5.157

Review 3.  Macrophages and polymorphonuclear neutrophils in lung defense and injury.

Authors:  Y Sibille; H Y Reynolds
Journal:  Am Rev Respir Dis       Date:  1990-02

4.  Small airways in idiopathic pulmonary fibrosis. Comparison of morphologic and physiologic observations.

Authors:  R G Crystal; J D Fulmer; W C Roberts; E R von Gal
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Review 5.  Cystic fibrosis: a disease in electrolyte transport.

Authors:  P M Quinton
Journal:  FASEB J       Date:  1990-07       Impact factor: 5.191

6.  Aerosol alpha 1-antitrypsin treatment for cystic fibrosis.

Authors:  N G McElvaney; R C Hubbard; P Birrer; M S Chernick; D B Caplan; M M Frank; R G Crystal
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7.  Macrophages cultured in vitro release leukotriene B4 and neutrophil attractant/activation protein (interleukin 8) sequentially in response to stimulation with lipopolysaccharide and zymosan.

Authors:  J A Rankin; I Sylvester; S Smith; T Yoshimura; E J Leonard
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

8.  Neutrophil elastase cleaves C3bi on opsonized pseudomonas as well as CR1 on neutrophils to create a functionally important opsonin receptor mismatch.

Authors:  M F Tosi; H Zakem; M Berger
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

9.  Generation of cAMP-activated chloride currents by expression of CFTR.

Authors:  M P Anderson; D P Rich; R J Gregory; A E Smith; M J Welsh
Journal:  Science       Date:  1991-02-08       Impact factor: 47.728

Review 10.  Cystic fibrosis. 2. Lung injury in cystic fibrosis.

Authors:  J S Elborn; D J Shale
Journal:  Thorax       Date:  1990-12       Impact factor: 9.139

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  130 in total

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5.  Quantitative analysis of inflammatory cells infiltrating the cystic fibrosis airway mucosa.

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Review 7.  Monitoring inflammation in CF. Cytokines.

Authors:  Scott D Sagel; Frank J Accurso
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Review 8.  The role of inflammation in the pathophysiology of CF lung disease.

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Journal:  Clin Rev Allergy Immunol       Date:  2002-08       Impact factor: 8.667

Review 9.  New perspectives in understanding and management of the respiratory disease in cystic fibrosis.

Authors:  S Suter
Journal:  Eur J Pediatr       Date:  1994-03       Impact factor: 3.183

Review 10.  Neutrophils in asthma.

Authors:  Ana L Macdowell; Stephen P Peters
Journal:  Curr Allergy Asthma Rep       Date:  2007-11       Impact factor: 4.806

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