Role of extracellular calcium in chrysotile asbestos stimulation of alveolar macrophages

Brian Kalla, Raymond F. Hamilton, Ronald K. Scheule, Andrij Holian

Research output: Contribution to journalArticlepeer-review

Abstract

The purpose of these studies was to determine whether extracellular calcium and calcium channels can influence chrysotile asbestos-stimulated production of superoxide anion by guinea pig alveolar macrophages. Increasing the extracellular calcium concentration from 0.0 to 10.0 mm markedly enhanced the ability of noncytotoxic levels of chrysotile (25 μg/ml) to stimulate macrophage production of superoxide anion at 37°C. The primary effect of increasing extracellular calcium was to prolong superoxide anion production. In parallel with these calcium-dependent effects on superoxide anion production, chrysotile also caused an elevation of cytosolic calcium (measured using Fura-2) which increased with increasing extracellular calcium concentrations. A number of organic calcium channel antagonists were tested for their ability to block chrysotile-stimulated superoxide anion production by cells in medium containing physiological levels of calcium. The relative order of potency of these antagonists was verapamil ≫ nimopidine ≈ diltiazem ≈ nifedipine > segontin. In parallel with its effects on superoxide anion production, verapamil also partially blocked the observed chrysotile-stimulated elevation of cytosolic calcium. Taken together, these results suggest that chrysotile can open calcium channels on the macrophage surface, allowing extracellular calcium to enter and contribute to the elevation of cytosolic calcium levels. This elevation of cytosolic calcium in turn serves to prolong chrysotile-stimulated superoxide anion production.

Original languageEnglish
Pages (from-to)130-138
Number of pages9
JournalToxicology and Applied Pharmacology
Volume104
Issue number1
DOIs
StatePublished - Jun 1 1990

Fingerprint

Dive into the research topics of 'Role of extracellular calcium in chrysotile asbestos stimulation of alveolar macrophages'. Together they form a unique fingerprint.

Cite this