Literature DB >> 3699139

Experimental lesions in rats corresponding to advanced human asbestosis.

J M Davis, R E Bolton, D Brown, H E Tully.   

Abstract

Rats inhaling chrysotile asbestos developed a progressive interstitial fibrosis similar in most respects to human asbestosis. The earliest lesions were focal deposits of fibrous tissue in the walls of respiratory bronchioles and alveolar ducts. Later alveolar septa between adjacent bronchioles became progressively thickened to produce lesions with similarities to human honeycombing. The thickened septa between alveoli or "micro-honeycomb" spaces were mainly surfaced with cuboidal epithelial cells although some spaces lined by ciliated columnar epithelium were also found. Transmission electron microscopy of these advanced lesions showed that the cuboidal epithelial cells retained most of the characteristics of type 2 pneumocytes but that they frequently exhibited apical cytoplasmic blebs normally associated with the apocrine secretion of Clara cells. Columnar cells exhibited all stages from fully cilitated to cells with only an occasional cilium among the normal cell surface microvilli. Alveolar or micro-honeycomb spaces frequently contained clusters of pulmonary macrophages with their surface processes interdigitated but with no signs of fusion to giant cells. At more than 18 months after the end of dust inhalation these macrophages contained no chrysotile asbestos. The basement membranes beneath the epithelial layers of thickened septa were irregular and often convoluted as well as being much thicker than normal. Microscopic deposits of calcification were frequently found within the basement membrane material. Some thickened septa were relatively acellular, consisting mainly of masses of collagen fibrils but others were cellular and contained many macrophages, fibroblasts, plasma cells and mast cells. In these advanced lesions extremely little chrysotile asbestos was found and this was present in two sites only. Some chrysotile, always as individual fibrils and usually of short length, was present among collagen fibrils in areas of fibrosis and some was present within the thickened basement membranes.

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Year:  1986        PMID: 3699139     DOI: 10.1016/0014-4800(86)90071-7

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  7 in total

1.  Asbestos related malignancy and the Cairns hypothesis.

Authors:  K Browne
Journal:  Br J Ind Med       Date:  1991-02

Review 2.  Low level exposure to asbestos: is there a cancer risk?

Authors:  J M Davis; J C McDonald
Journal:  Br J Ind Med       Date:  1988-08

3.  Comparisons of the pathogenicity of long and short fibres of chrysotile asbestos in rats.

Authors:  J M Davis; A D Jones
Journal:  Br J Exp Pathol       Date:  1988-10

4.  Activated human peripheral blood neutrophils produce epithelial injury and fibronectin breakdown in vitro.

Authors:  D M Brown; G M Brown; W Macnee; K Donaldson
Journal:  Inflammation       Date:  1992-02       Impact factor: 4.092

5.  Experimental studies in rats on the effects of asbestos inhalation coupled with the inhalation of titanium dioxide or quartz.

Authors:  J M Davis; A D Jones; B G Miller
Journal:  Int J Exp Pathol       Date:  1991-10       Impact factor: 1.925

Review 6.  The relationship between fibrosis and cancer in experimental animals exposed to asbestos and other fibers.

Authors:  J M Davis; H A Cowie
Journal:  Environ Health Perspect       Date:  1990-08       Impact factor: 9.031

Review 7.  The role of clearance and dissolution in determining the durability or biopersistence of mineral fibers.

Authors:  J M Davis
Journal:  Environ Health Perspect       Date:  1994-10       Impact factor: 9.031

  7 in total

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