Literature DB >> 7757173

Differential release of superoxide anions by macrophages treated with long and short fibre amosite asbestos is a consequence of differential affinity for opsonin.

I M Hill1, P H Beswick, K Donaldson.   

Abstract

OBJECTIVE: To investigate the ability of short and long fibre samples of amosite asbestos to stimulate superoxide production in isolated rat alveolar macrophages, and to determine how opsonisation with rat immunoglobulin might modify this response.
METHODS: Macrophages were isolated from rat lung by bronchoalveolar lavage and challenged with both opsonised and non-opsonised long and short fibres of amosite asbestos. Release of superoxide anions was measured by the spectrophotometric reduction of cytochrome c, in the presence and absence of superoxide dismutase.
RESULTS: Both long and short fibre samples of amosite asbestos without opsonisation were ineffective in stimulating isolated rat alveolar macrophages to release superoxide anions in vitro. After opsonisation with immunoglobulin, however, a dramatic enhancement of release of superoxide anion was seen with long fibres, but not short, which confirms the importance of fibre length in mediating biological effects. The increased biological activity of the long fibre sample is explained by increased binding of the opsonin to the fibre surface as, at equal mass, the long fibres bound threefold more immunoglobulin than the short fibres.
CONCLUSION: Opsonisation is an important factor in modulation of the biological activity of fibres at the cellular level. Differences in binding of opsonin to samples of fibre previously considered to be identical apart from length, suggest that surface reactivity needs to be taken into account when fibres are compared. Binding of biological molecules, in vivo, may thus be an important modifying factor in the pathological processes initiated by fibres.

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Year:  1995        PMID: 7757173      PMCID: PMC1128161          DOI: 10.1136/oem.52.2.92

Source DB:  PubMed          Journal:  Occup Environ Med        ISSN: 1351-0711            Impact factor:   4.402


  32 in total

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Authors:  N S Dalal; M M Suryan; V Vallyathan; F H Green; B Jafari; R Wheeler
Journal:  Ann Occup Hyg       Date:  1989

Review 4.  Immunoglobulin G and its function in the human respiratory tract.

Authors:  H Y Reynolds
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5.  Radioiodination of proteins by the use of the chloramine-T method.

Authors:  P J McConahey; F J Dixon
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

6.  Generation of superoxide (O2-.) from alveolar macrophages exposed to asbestiform and nonfibrous particles.

Authors:  K Hansen; B T Mossman
Journal:  Cancer Res       Date:  1987-03-15       Impact factor: 12.701

7.  Role of reactive oxygen metabolites in crocidolite asbestos toxicity to mouse macrophages.

Authors:  L A Goodglick; A B Kane
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Authors:  V Vallyathan; X L Shi; N S Dalal; W Irr; V Castranova
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10.  The pathogenicity of long versus short fibre samples of amosite asbestos administered to rats by inhalation and intraperitoneal injection.

Authors:  J M Davis; J Addison; R E Bolton; K Donaldson; A D Jones; T Smith
Journal:  Br J Exp Pathol       Date:  1986-06
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  10 in total

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2.  Chemical differences between long and short amosite asbestos: differences in oxidation state and coordination sites of iron, detected by infrared spectroscopy.

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Review 4.  Asbestos, carbon nanotubes and the pleural mesothelium: a review of the hypothesis regarding the role of long fibre retention in the parietal pleura, inflammation and mesothelioma.

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Authors:  M Ohyama; T Otake; K Morinaga
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Review 6.  Surface reactivity in the pathogenic response to particulates.

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Journal:  Environ Health Perspect       Date:  1997-09       Impact factor: 9.031

Review 7.  Mechanisms of fiber-induced genotoxicity.

Authors:  M C Jaurand
Journal:  Environ Health Perspect       Date:  1997-09       Impact factor: 9.031

8.  Multiwall Carbon Nanotube-Induced Apoptosis and Antioxidant Gene Expression in the Gills, Liver, and Intestine of Oryzias latipes.

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9.  Functional consequences for primary human alveolar macrophages following treatment with long, but not short, multiwalled carbon nanotubes.

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10.  Microstructures and nanostructures for environmental carbon nanotubes and nanoparticulate soots.

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  10 in total

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