Oxidized ATP. An irreversible inhibitor of the macrophage purinergic P2Z receptor

• Published in: The Journal of biological chemistry 1993-04, Vol.268 (11), p.8199-8203
• Main Authors: MURGIA, M, HANAU, S, PIZZO, P, RIPPA, M, DI VIRGILIO, F
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - analogs & derivatives; Adenosine Triphosphate - pharmacology; Animals; Biological and medical sciences; Biological Transport - drug effects; Cell Line; Cell Membrane - drug effects; Cell Membrane - metabolism; Cell Membrane - physiology; Cell Membrane Permeability; Cell receptors; Cell structures and functions; Ethidium - metabolism; Fundamental and applied biological sciences. Psychology; Kinetics; L-Lactate Dehydrogenase - metabolism; Macrophages - metabolism; Membrane Potentials - drug effects; Mice; Miscellaneous; Molecular and cellular biology; Purinergic Antagonists; Vacuoles - drug effects
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)53082-9

The effects of oxidized ATP (oATP) on responses triggered by extracellular adenosine 5'-triphosphate (ATPe) were investigated in the mouse macrophage-like cell line J774. ATPe induced in this cell line two kinds of responses mediated by two different P2 purinergic receptors: 1) an early permeabilization of the plasma membrane to extracellular hydrophilic markers of M(r) up to 900 mediated by P2Z receptors; and 2) a fast mobilization of Ca2+ from intracellular stores mediated by P2Y receptors. Low oATP concentrations (100 microM) completely blocked the first response without affecting the second. ATPe-dependent cell swelling, vacuolization, and lysis were also inhibited. Antagonism developed slowly, as an incubation at 37 degrees C for at least 2 h in the presence of oATP was needed and was irreversible, thus suggesting that the inhibitory action was due to covalent modification of the receptor. The rate of hydrolysis of exogenous ATP was slightly decreased by oATP, indicating a minor blocking effect of this compound on plasma membrane ecto-ATPases in the concentration range tested. These observations suggest that oATP may be a potentially very useful tool for isolation and characterization of the P2Z purinergic receptor.