Expression of genes coding for growth factors in experimental pneumoconiosis

Chest

Volumn 109, Issue 3 SUPPL., 1996, Pages 45S-49S

  Morris, Gilbert F ^a   Liu, Jing Yao ^a   Lei, Wei Hong ^a   Brody, Arnold R ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASBESTOS FIBER; GROWTH FACTOR; MESSENGER RNA; PLATELET DERIVED GROWTH FACTOR; TRANSCRIPTION FACTOR; TRANSFORMING GROWTH FACTOR ALPHA; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL MODEL; ANIMAL TISSUE; ASBESTOSIS; CELL PROLIFERATION; CHRONIC LUNG DISEASE; CONFERENCE PAPER; GENE ACTIVATION; GENE EXPRESSION; LUNG FIBROSIS; MACROPHAGE ACTIVATION; NONHUMAN; PNEUMOCONIOSIS; PRIORITY JOURNAL; RAT;

ANIMALS; ASBESTOS; DISEASE MODELS, ANIMAL; GENE EXPRESSION REGULATION; PLATELET-DERIVED GROWTH FACTOR; PNEUMOCONIOSIS; RNA, MESSENGER;

EID: 0029939424     PISSN: 00123692     EISSN: None     Source Type: Journal    
DOI: 10.1378/chest.109.3_Supplement.45S-a     Document Type: Article

References (55)

1. Brody AR. Production of cytokines by particle-exposed lung macrophages. In: Brinkley W, Lechner J, Harris C, eds. Cellular and molecular aspects of fiber carcinogenesis. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1991;
2. Perkins RC, Scheule RK, Hamilton R, et al. Human alveolar macrophage cytokine release in response to in vitro and in vivo asbestos exposure. Exp Lung Res 1993; 19:55-65
3. Rom WN, Travis WD, Brody AR. Cellular and molecular basis of the asbestos-related diseases. Am Rev Respir Dis 1991; 143: 408-22
4. Driscoll KE, Hassenbein DG, Carter J, et al. Macrophage inflammatory proteins 1 and 2: expression by rat alveolar macrophages, fibroblasts, and epithelial cells and in rat lung after mineral dust exposure. Am J Respir Cell Mol Biol 1993; 8:311-18
5. Crouch E. Pathobiology of pulmonary fibrosis. Am J Physiol 1990; 259:L159-79
6. Crystal R, Fulmer J, Roberts W, et al. Idiopathic pulmonary fibrosis: clinical, histologic, radiographic, physiologic, scintigraphic, cytologic, and biochemical aspects. Ann Intern Med 1976; 85:769-78
7. Marinelli WA, Henke CA, Harmon KR, et al. Mechanisms of alveolar fibrosis after acute lung injury. Clin Chest Med 1990; 11:657-72
8. Davis GS. Pathogenesis of silicosis: current concepts and hypotheses. Lung 1986; 164:1-16
9. Nathan C. Secretory products of macrophages. J Clin Invest 1987; 79:319-27
10. Kelly J. Cytokines of the lung. Am Rev Respir Dis 1990; 141: 765-88
11. Xing Z, Jordana M, Kirpalani H, et al. Cytokine expression by neutrophils and macrophages in vivo: endotoxin induces tumor necrosis factor-alpha, macrophage inflammatory protein-2, interleukin-1 beta, and interleukin-6 but not RANTES of transforming growth factor-beta 1 mRNA expression in acute lung inflammation. Am J Respir Cell Mol Biol 1994; 10:148-53
12. Bonner JC, Osornio-Vargas AR, Badgett A, et al. Differential proliferation of rat lung fibroblasts induced by platelet-derived growth factor -AA, -AB, and -BB isoforms secreted by alveolar macrophages. Am J Respir Cell Mol Biol 1991; 5:539-47
13. Bauman MB, Jetten AM, Bonner JC, et al. Secretion of platelet-derived growth factor homologue by rat alveolar macrophages exposed to particulates in vitro. Eur J Cell Biol 1990; 51:327-34
14. Lasky JA, Bonner JC, Brody AR. The pathobiology of asbestos-induced lung disease: a proposed role for macrophage-derived growth factors. Ann NY Acad Sci 1991; 643:239-44
15. Marsh JP, Mossman BT, Driscoll KE, et al. Effects of aramid, a high strength synthetic fiber, on respiratory cells in vitro. Drug Chem Toxicol 1994; 1994:75-92
16. Leikauf GD, Fink SP, Miller ML, et al. Refractory ceramic fibers activate alveolar macrophage eicosanoid and cytokine release. J Appl Physiol 1995; 78:164-71
17. Brody AR. Asbestos exposure as a model of inflammation inducing interstitial pulmonary fibrosis. In: Gallin JI, Goldstein JH, Snyderman R, eds. Inflammation: basic principles and clinical correlates. New York: Raven Press, 1992; 1033-49
18. Brody AR, Roe MW. Deposition pattern of inorganic particles at the alveolar level in the lungs of rats and mice. Am Rev Respir Dis 1983; 128:724-32
19. Brody AR, Hill LH, Adkins B, et al. Chrysotile asbestos inhalation in rats: deposition pattern and reaction of alveolar epithelium and pulmonary macrophages. Am Rev Respir Dis 1981; 123: 670-79
20. Roggli V, Brody AR. Changes in numbers and dimensions of chrysotile asbestos fibers in lungs of rats following short-term exposure. Exp Lung Res 1984; 7:133-47
21. McGavran PD, Butterick CJ, Brody AR. Tritiated thymidine incorporation and the development of an interstitial lesion in the bronchiolar-alveolar regions of normal and complement-deficient mice after inhalation of chrysotile asbestos. J Environ Pathol Toxicol Oncol 1990; 6:377-88
22. Warheit DB, George G, Hill LH, et al. Inhaled asbestos activates a complement-dependent chemotactic factor for macrophages. Lab Invest 1985; 52:505-14
23. Warheit DB, Hill LH, George G, et al. Time course of chemotactic factor generation and the corresponding macrophage response to asbestos inhalation. Am Rev Respir Dis 1986; 134: 128-33
24. Brody AR, Hill LH. Interstitial accumulation of inhaled chrysotile asbestos fibers and consequent formation of microcalcifications. Am J Pathol 1982; 109:107-14
25. Chang LY, Overby LH, Brody AR, et al. Progressive lung cell reactions and extracellular matrix production after a brief exposure to asbestos. Am J Pathol 1988; 131:156-70
26. Brody AR, Overby LH. Incorporation of tritiated thymidine by epithelial and interstitial cells in bronchiolar-alveolar regions of asbestos-exposed rats. Am J Pathol 1989; 134:133-40
27. Crystal RG, Ferrans VJ, Basset F. Biologic basis of pulmonary fibrosis. In: Crystal RG, West JB, eds. The lung: scientific foundations. New York: Raven Press, 1991; 2031-46
28. Kovacs EJ, DiPietro LA. Fibrogenic cytokines and connective tissue production. FASEB J 1994; 8:854-61
29. Vanhee D, Gosset P, Wallaert B, et al. Role of macrophage-derived cytokines in coal workers' pneumoconioisis. Ann NY Acad Sci 1994; 725-183-92
30. Scheule RK, Holian A. Immunologic aspects of pneumoconiosis. Exp Lung Res 1991; 17:661-85
31. Piquet PF. Cytokines involved in pulmonary fibrosis. Int Rev Exp Pathol 1993; 34(pt B):173-81
32. Brody AR. Control of lung fibroblast proliferation by macrophage-derived platelet-derived growth factor. Ann NY Acad Sci 1994; 275:193-206
33. Gauldie J, Jordana M, Cox G. Cytokines and pulmonary fibrosis. Thorax 1993; 48:931-35
34. Claesson-Welsh L. Platelet-derived growth factor receptor signals. J Biol Chem 1994; 269:32023-26
35. Westermark B, Heldin CH. Platelet-derived growth factor: structure, function and implications in normal and malignant cell growth. Acta Oncol 1993; 32:101-05
36. Bonner JC, Goodell AL, Coin PG, et al. Chrysotile asbestos up-regulates gene expression and production of alpha-receptors for platelet-derived growth factor (PDGF-AA) on rat lung fibroblasts. J Clin Invest 1993; 92:425-30
37. Lasky JA, Coin PG, Lindroos PM, et al. Chrysotile asbestos stimulates platelet-derived growth factor-AA production by rat lung fibroblasts in vitro: evidence for an autocrine loop. Am J Respir Cell Mol Biol 1995; 12:162-70
38. Walker C, Bermudez E, Stewart W, et al. Characterization of platelet-derived growth factor and platelet-derived growth factor receptor expression in asbestos-induced rat mesothelioma. Cancer Res 1992; 52:301-06
39. Fitzpatrick DR, Peroni DJ, Bielefeldt-Ohmann H. The role of growth factors and cytokines in the tumorigenesis and immunobiology of malignant mesothelioma. Am J Respir Cell Mol Biol 1995; 12:455-60
40. Perdue TD, Brody AR. Distribution of transforming growth factor B1, fibronectin, and smooth muscle actin in asbestos-induced pulmonary fibrosis in rats. J Histochem Cytochem 1994; 42: 1061-70
41. Lin X, Wang ZLG, Deuel TF. Functional analysis of the human platelet-derived growth factor A-chain promoter region. J Biol Chem 1992; 267:25614-19
42. Heintz NH, Janssen YM, Mossman BT. Persistant induction of c-fos and c-jun expression by asbestos. Proc Natl Acad Sci USA 1993; 90:3299-3303
43. Janssen YMW, Heintz NH, Marsh JP, et al. Induction of c-fos and c-jun in target cells of the lung and pleura by carcinogenic fibers. Am J Respir Cell Mol Biol 1994; 11:522-30
44. Quinlan TR, Marsh JP, Janssen YMW, et al. Dose-responsive increases in pulmonary fibrosis after inhalation of asbestos. Am J Respir Crit Care Med 1994; 150:200-06
45. Hill CS, Treisman R. Transcriptional regulation by extracellular signals: mechanisms and specificity. Cell 1995; 80:199-211
46. Kamp DW, Graceffa P, Pryor WA, et al. The role of free radicals in asbestos-induced diseases. Free Radic Biol Med 1992; 12:283-315
47. Perderiset M, Marsh JP, Mossman BT. Activation of protein kinase C by crocidilite asbestos in hamster tracheal epithelial cells. Carcinogenesis 1991; 12:1499-1502
48. Simeonova PP, Luster MI. Iron and reactive oxygen species in the asbestos-induced tumor necrosis factor-alpha response from alveolar macrophages. Am J Respir Cell Mol Biol 1995; 12:676-83
49. Holley JA, Janssen YM, Mossman BT, et al. Increased manganese superoxide dismutase protein in type II epithelial cells of rat lungs after inhalation of crocidilite asbestos or cristobalite silica. Am J Pathol 1992; 141:475-85
50. Quinlan TR, Marsh JP, Janssen YMW, et al. Oxygen radicals and asbestos-mediated disease. Environ Health Perspect 1994; 102(suppl 10):107-10
51. Janssen YM, Marsh JP, Assher MP, et al. Expression of antioxidant enzymes in rat lungs after inhalation of asbestos or silica. J Biol Chem 1992; 267:10625-30
52. Janssen YM, Heintz NH, Mossman BT. Induction of c-fos and c-jun proto-oncogene expression by asbestos is ameliorated by N-acetyl-L-cysteine in mesothelial cells. Cancer Res 1995; 15: 2085-89
53. Thomas G, Ando T, Verma K, et al. Asbestos fibers and interferon-gamma upregulate nitric oxide production in rat alveolar macrophages. Am J Respir Cell Mol Biol 1994; 11:707-15
54. Ausubel FM, Brent R, Kingston RE, et al. Current protocols in molecular biology. New York: John Wiley & Sons, 1994
55. Morris GF, Mathews MB. The adenovirus E1A transforming protein activates the proliferating cell nuclear antigen promoter via an activating transcription factor site. J Virol 1991; 65:6397-6406