. (1972). Brit. J. industr. Med., 29,[280][281][282][283][284][285][286] Comparison of effects on macrophage cultures of glass fibre, glass powder, and chrysotile asbestos. The effects on macrophage cultures of glass fibre, glass powder, and chrysotile asbestos are compared. Glass fibre behaves like chrysotile in producing an increase in cell membrane permeability in cultured macrophages. This is demonstrable by the increase in lactic dehydrogenase activity in the supernatant fluid. The metabolism, measured by lactate production, is not reduced as it is when quartz is phagocytosed. Glass powder behaves like the inert dust corundum, producing little change in the number of cells stained by erythrosin B and a small increase in lactate dehydrogenase activity, both being in the range of the control. There is an increase in lactate production as a result of higher metabolism due to phagocytosis. Dusts may produce two basic effects, namely a toxic effect and change in cell membrane permeability. A non-specific effect on the cell membrane due to the slow and sometimes incomplete process of ingestion of long fibres is probably a function of the morphology, particularly the length of the fibres. A primary specific effect induced by some dusts immediately follows contact with the cell membrane.Recent investigations have shown that asbestos fibres alter the permeability of the membrane of cells cultured in vitro. Koshi, Hayashi, and Sakabe (1968) demonstrated an increase in the acid phosphatase released from the cells into the culture medium when rat peritoneal macrophages were incubated with asbestos. Beck (1970) and Beck, Holt, and Nasrallah (1971) found that chrysotile asbestos added to cultures of alveolar or peritoneal macrophages increased the number of cells stained with erythrosin and increased the amount of lactic dehydrogenase (LDH) released into the culture medium.To determine whether the shape, the length or the chemical composition of the fibres is the factor influencing the permeability of the cell membrane, cultures of inacrophages were incubated with two types of fibrous material, chrysotile and glass fibre. In each case the permeability of the cell membrane was determined by estimating the percentage of cells that stained with erythrosin B and the LDH activity in the supernatant. The vitality of the cells was measured by the rate of lactate production. Controls were run with no addition of dust, with quartz powder (toxic), and with corundum powder (inert). Materials Chrysotile A high-grade Rhodesian chrysotile was opened in the mill of a dust tunnel (Holt, Mills, and Young, 1964).Glass fibre A dust was prepared in the same way from commercially available glass fibre. The sample ranged in length from I to 20 ptm and in diameter from 0-25 to 1 0 ,um.
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