Characteristics of ATP-Induced Current Through P2X7 Receptor in NG108-15 Cells: Unique Antagonist Sensitivity and Lack of Pore Formation

The Japanese Journal of Pharmacology

Junko Kimura¹  Isao Matsuoka¹  Tomokazu Watano¹ 

[1] Department of Pharmacology, Fukushima Medical University School of Medicine

关键词: ATP;    P2X7 receptor;    Antagonist;    Pore formation;    NG108-15 cell;   

DOI  :  10.1254/jjp.88.428

学科分类：药理学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(41)Cited-By(10)ATP activates the mouse P2X7 receptor and induces a nonselective-cation current in NG108-15 cells. We investigated the effects of five receptor antagonists on the ATP-induced nonselective-cation current through P2X7 receptor (INS · P2X7) in NG108-15 cells. Nonselective P2 receptor antagonists, RB-2, PPADS and suramin inhibited the INS · P2X7 with IC50 values of 4.3, 53 and 40 μM, respectively. However, KN-04, which is a potent antagonist of human P2X7 receptors but is not that of rat P2X7 receptors, had only a weak blocking effect. Furthermore, oxidized-ATP (300 μM), an antagonist of the P2X7 receptor-mediated pore-formation, did not affect the INS · P2X7. Prolonged ATP application did not increase the membrane permeability to large molecules, N-methyl-D-glucamine or Yo-Pro-1, indicating that pore-formation was not promoted by the P2X7 receptor activation in NG108-15 cells. These results suggest that antagonist sensitivities and pore-forming properties of the P2X7 receptors in NG108-15 cells are different from those of other cells types.

【 授权许可】

Unknown