Affiliation:
1. Centre hospitalier de l'Université de Montréal and Department of Medicine, Université de Montréal, Montréal, Québec, Canada H2W 1T8
Abstract
ATP release induced by hypotonic swelling is an ubiquitous phenomenon in eukaryotic cells, but its underlying mechanisms are poorly defined. A mechanosensitive (MS) ATP channel has been implicated because gadolinium (Gd3+), an inhibitor of stretch-activated channels, suppressed ATP efflux monitored by luciferase bioluminescence. We examined the effect of Gd3+on luciferase bioluminescence and on ATP efflux from hypotonically swollen cells. We found that luciferase was inhibited by ≤10 μM Gd3+, and this may have contributed to the previously reported inhibition of ATP release. In ATP efflux experiments, luciferase inhibition could be prevented by chelating Gd3+with EGTA before luminometric ATP determinations. Using this approach, we found that 10–100 μM Gd3+, i.e., concentrations typically used to block MS channels, actually stimulated hypotonically induced ATP release from fibroblasts. Inhibition of ATP release required at least 500, 200, or 100 μM Gd3+ for fibroblasts, A549 cells, and 16HBE14o− cells, respectively. Such biphasic and cell-specific effects of Gd3+ are most consistent with its action on membrane lipids and membrane-dependent processes such as exocytosis.
Publisher
American Physiological Society
Cited by
82 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献