Abstract
Evidence on the mechanism by which inhaled mineral fibres lead to pulmonary fibrosis has not been forthcoming. As with silica, a biphasic cell culture system was required to distinguish phagocytosis from collagen formation. Synthesis of total protein and collagen by rat fibroblasts was estimated by incorporation of labelled proline after treatment with the medium from rat peritoneal macrophages that had been cultured in the presence of different types of mineral fibre. The influence of fibre length was also examined. All the main varieties of asbestos reacted with macrophages to produce or release a fibrogenic factor. However, chrysotile and the longer amosite fibres evoked the response only after prolonging the period of incubation with macrophages, presumably by permitting more complete phagocytosis of curled or longer fibres. Short amosite fibres proved to be more active than longer ones and under certain conditions were as potent as quartz. Fibrous glass also possessed stimulatory properties and again a sample having a short length gave a stronger response than a long one. Collagen formation by asbestos thus appears to be mediated by a macrophage factor, so operating in a manner similar to that previously demonstrated for quartz. The conventional view that short fibres are comparatively insignificant in asbestos fibrogenesis cannot, on the present evidence, be sustained. Furthermore, it should not be assumed than man-made mineral fibres of respirable diameter are innocuous or that short ones can be ignored.
Full text
PDF








Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brody A. R., Hill L. H., Adkins B., Jr, O'Connor R. W. Chrysotile asbestos inhalation in rats: deposition pattern and reaction of alveolar epithelium and pulmonary macrophages. Am Rev Respir Dis. 1981 Jun;123(6):670–679. doi: 10.1164/arrd.1981.123.6.670. [DOI] [PubMed] [Google Scholar]
- Civil G. W., Heppleston A. G. Replenishment of alveolar macrophages in silicosis: implication of recruitment by lipid feed-back. Br J Exp Pathol. 1979 Oct;60(5):537–547. [PMC free article] [PubMed] [Google Scholar]
- Goldstein R. H., Miller K., Glassroth J., Linscott R., Snider G. L., Franzblau C., Polgar P. Influence of asbestos fibers on collagen and prostaglandin production in fibroblast and macrophage co-cultures. J Lab Clin Med. 1982 Nov;100(5):778–785. [PubMed] [Google Scholar]
- Heppleston A. G. Silicotic fibrogenesis: a concept of pulmonary fibrosis. Ann Occup Hyg. 1982;26(1-4):449–462. [PubMed] [Google Scholar]
- Heppleston A. G., Styles J. A. Activity of a macrophage factor in collagen formation by silica. Nature. 1967 Apr 29;214(5087):521–522. doi: 10.1038/214521a0. [DOI] [PubMed] [Google Scholar]
- Holt P. F., Mills J., Young D. K. Experimental asbestosis with four types of fibers: importance of small particles. Ann N Y Acad Sci. 1965 Dec 31;132(1):87–97. doi: 10.1111/j.1749-6632.1965.tb41092.x. [DOI] [PubMed] [Google Scholar]
- Pooley F. D., Clark N. Fiber dimensions and aspect ratio of crocidolite, chrysotile and amosite particles detected in lung tissue specimens. Ann N Y Acad Sci. 1979;330:711–716. doi: 10.1111/j.1749-6632.1979.tb18775.x. [DOI] [PubMed] [Google Scholar]
- Yeager H., Jr, Russo D. A., Yañez M., Gerardi D., Nolan R. P., Kagan E., Langer A. M. Cytotoxicity of a short-fiber chrysotile asbestos for human alveolar macrophages: preliminary observations. Environ Res. 1983 Feb;30(1):224–232. doi: 10.1016/0013-9351(83)90182-2. [DOI] [PubMed] [Google Scholar]
