z-logo
open-access-imgOpen Access
Cell swelling-induced ATP release and gadolinium-sensitive channels
Author(s) -
Francis Boudreault,
Ryszard Grygorczyk
Publication year - 2002
Publication title -
ajp cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.432
H-Index - 181
eISSN - 1522-1563
pISSN - 0363-6143
DOI - 10.1152/ajpcell.00317.2001
Subject(s) - luciferase , biophysics , chemistry , egta , bioluminescence , efflux , exocytosis , microbiology and biotechnology , biochemistry , membrane , biology , calcium , transfection , organic chemistry , gene
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 (Gd(3+)), an inhibitor of stretch-activated channels, suppressed ATP efflux monitored by luciferase bioluminescence. We examined the effect of Gd(3+) on luciferase bioluminescence and on ATP efflux from hypotonically swollen cells. We found that luciferase was inhibited by < or =10 microM Gd(3+), and this may have contributed to the previously reported inhibition of ATP release. In ATP efflux experiments, luciferase inhibition could be prevented by chelating Gd(3+) with EGTA before luminometric ATP determinations. Using this approach, we found that 10-100 microM Gd(3+), 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 microM Gd(3+) for fibroblasts, A549 cells, and 16HBE14o(-) cells, respectively. Such biphasic and cell-specific effects of Gd(3+) are most consistent with its action on membrane lipids and membrane-dependent processes such as exocytosis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom