Apoptosis and extracellular matrix remodelling in human silicosis

Histopathology

Volumn 49, Issue 3, 2006, Pages 283-289

  Delgado, L ^a   Parra, E R ^a   Capelozzi, V L ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Bcl 2; Extracellular matrix; Fas L; Mast cells; Silicosis

Indexed keywords

COLLAGEN; FAS LIGAND; PROTEIN BCL 2; SILICON DIOXIDE;

APOPTOSIS; ARTICLE; CHRONIC DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE MARKER; DISEASE SEVERITY; ELASTIC FIBER; EXTRACELLULAR MATRIX; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFLAMMATION; INFLAMMATORY CELL; LUNG BIOPSY; MAST CELL; MORPHOMETRICS; OCCUPATIONAL DISEASE; PRIORITY JOURNAL; QUANTITATIVE DIAGNOSIS; QUANTITATIVE STUDY; SILICOSIS; TISSUE INJURY;

APOPTOSIS; COLLAGEN; ELASTIC TISSUE; EXTRACELLULAR MATRIX; FAS LIGAND PROTEIN; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; IMMUNOHISTOCHEMISTRY; MAST CELLS; MEMBRANE GLYCOPROTEINS; PROTO-ONCOGENE PROTEINS C-BCL-2; SILICOSIS; TUMOR NECROSIS FACTORS;

EID: 33747387967     PISSN: 03090167     EISSN: 13652559     Source Type: Journal    
DOI: 10.1111/j.1365-2559.2006.02477.x     Document Type: Article

References (28)

1. Rom WN, Bitterman PB, Rennard SI et al. Characterization of the lower respiratory tract inflammation of nonsmoking individuals with interstitial lung disease associated with chronic inhalation of inorganic dusts. Am. Rev. Respir. Dis. 1987; 136; 1429-1434.
2. Weill H, Jones RN, Parkes WR. Silicosis and related diseases. In Parks WR ed. Occupational lung disorders, 3rd edn. Oxford: Butterworth-Heinemann 1994; 285-339.
3. Mosmann B, Churg A. Mechanism in the pathogenesis of asbestosis and silicosis. Am. J. Respir. Crit. Care Med. 1998; 157; 1666-1680.
4. Tomokuni A, Otsuki T, Isozaki Y et al. Serum levels of soluble Fas-ligand in patients with silicosis. Clin. Exp Immunol. 1999; 118; 441-444.
5. Borges VM, Falcäo H, Leite-Junior JH et al. Fas-ligand triggers pulmonary silicosis. J. Exp. Med. 2001; 194; 155-164.
6. Borges VM, Lopes MF, Falcäo H et al. Apoptosis underlies immunopathogenic mechanisms in acute silicosis. Am. J. Respir. Cell. Mol. Biol. 2002; 27; 78-84.
7. Hnizdo E, Vallyathan V. Chronic obstructive pulmonary disease due to occupational exposure to silica dust: a review of epidemiological and pathological evidence. Occup. Environ. Med. 2003; 60; 237-243.
8. Hamzouzi A, Ammar J, Grairi H et al. Expression of Fas antigen and Fas-ligand in bronchoalveolar lavage from silicosis patients. Med. Inflamm. 2003; 12; 209-214.
9. Naohito S, Tadashi H, Otha K et al. Mast cells are essential for the full development of silica-induced pulmonary inflammation: a study with mast cell-deficient mice. Am. J. Respir. Cell. Mol. Biol. 1993; 9; 475-483.
10. Goto T, Befus D, Low R et al. Mast cells heterogeneity and hyperplasia in bleomycin-induced pulmonary fibrosis in rats. Am. Rev. Respir. Dis. 1984; 130; 797-802.
11. Watanabe S, Watanabe K, Ohnishi T et al. Mast cells in the rat alveolar septa undergoing fibrosis after ionizing irradiation. Lab. Invest. 1974; 31; 555-567.
12. Wagner MF, Edwards RE, Moncraft CB et al. Mast cells and inhalation of asbestos in rats. Thorax 1984; 39; 539-544.
13. Faffe D, Silva GH, Kurtz PM et al. Lung tissue mechanisms and extracellular matrix composition in a murine model of silicosis. J. Appl. Physiol. 2001; 90; 1400-1406.
14. Ueki A. Fas-Fasligand system in silicosis patients. Nippon Eiseigaku Zasshi 2000; 55; 474-480.
15. Battlehner CN, Carneiro Filho M, Ferreira Junior JM et al. Histochemical and ultrastructural study of the extracellular matrix fibres in patellar tendon donor site scars and normal controls. J. Submicrosc. Cytol. Pathol. 1996; 28; 175-186.
16. Montes GS. Structural biology of the fibers of the collagenous and elastic systems. Cell. Biol. Int. 1996; 20; 15-27.
17. Leick-Maldonado EA, Lemos M, Tiberio IF et al. Differential distribution of elastic system fibers in control and bronchoconstricted intraparenchymatous airways in the guinea-pig lung. J. Submicrosc. Cytol. Pathol. 1997; 29; 427-434.
18. Lemos M, Pozo RM, Montes GS et al. Organization of collagen and elastic fibers studied in stretch preparations of whole mounts of human visceral pleura. Anat. Ann. 1997; 179; 447-452.
19. Weibel ER, Cruz-Orive LM. Morphometric methods. In Crystal RG, West JBB eds. The lung. Philadelphia: Scientific Foundation, Lippincot-Raven Publishers 1977; 333-344.
20. Norusis MJ. SPSS for Windows [10.0]. Chicago: SPSS Inc. 2002.
21. Ueki A, Isozaki Y, Tomokuni A et al. Intramolecular epitope spreading among anti-caspase 8 auto antibodies in patients with silicosis, systemic sclerosis and systemic lupus erythematosus, as well as in healthy individuals. Clin. Exp. Immunol. 2002; 129; 556-561.
22. Kamal D, Srivastava W, Jaishree J et al. Crucial role of interleukin 1 beta and nitric oxide synthase in silica induced inflammation and apoptosis in mice. Am. J. Respir. Crit. Care Med. 2002; 165;527-533.
23. Nakajima H, Oka T. Analysis of biochemical and biological functions of Fas-L (Fas-L) and Fas on activated T cells in allo-immune response. Transplant. Proc. 1997; 29; 1096-1100.
24. Corsini E, Giani A, Lucchi L et al. Resistance to acute silicosis in senescent rats: role of alveolar macrophages. Chem. Res. Toxicol. 2003; 16; 1520-1527.
25. Lynch SE. Interactions of growth factors in tissue repair. Prog. Clin. Biol. Res. 1991; 365; 341-357.
26. Pierce GF, Tarpley JE, Yanagihara D et al. Platelet-derived growth factor (BB homodimer), transforming growth factor-1, and basic fibroblast growth factor in dermal wound healing: neovessel and matrix formation and cessation of repair. Am. J. Pathol. 1992; 140; 1375-1388.
27. Pesci A, Bertorelli G, Gabrielli M et al. Mast cells in fibrotic lung disorders. Chest 1993; 103; 989-996.
28. Barbas-Filho JV, Ferreira MA, Capelozzi VL et al. Evidence of type II pneumocyte apoptosis in the pathogenesis of idiopathic pulmonary fibrosis (IFP)/usual interstitial pneumonia (UIP). J. Clin. Pathol. 2001; 54; 132-138.