Am. J. Respir. Crit. Care Med., Vol 150, No. 1, 07 1994, 200-206.
Dose-responsive increases in pulmonary fibrosis after inhalation of asbestos
TR Quinlan, JP Marsh, YM Janssen, KO Leslie, D Hemenway, P Vacek and BT Mossman
Department of Pathology, University of Vermont, Burlington 05405.
We focused here on steady-state mRNA levels of genes involved in
antioxidant defense, i.e., manganese superoxide dismutase and copper- zinc
superoxide dismutase, and in cell proliferation, i.e., ornithine
decarboxylase, c-jun, and glyceraldehyde-3-phosphate-dehydrogenase in
whole-lung homogenates from Fischer 344 rats at 3 h to 20 d after exposure
to crocridolite asbestos. Changes in gene expression were correlated with
histopathologic findings, total and differential cell counts in
bronchoalveolar lavage, and levels of hydroxyproline in lung.
Dosage-dependent increases in mRNA levels of antioxidant enzymes and
proliferation-related genes were observed. Differential cell counts
revealed a dose-related infiltration of neutrophils that preceded
elevations in gene expression. Neutrophil infiltration into lung and focal
lesions of fibrosis as well as increased levels of hydroxyproline were
observed only at high concentrations of asbestos. These results indicate
that high airborne concentrations of asbestos cause molecular changes in
lung that may be related to antioxidant defense and the triggering of cell
proliferation, a feature of asbestosis and lung cancer.
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Copyright © 1994 American Thoracic Society
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