Human melanomas express functional P2X7 receptors

被引:54
作者
White, N
Butler, PEM
Burnstock, G
机构
[1] UCL Royal Free & Univ Coll Med Sch, Auton Neurosci Ctr, London NW3 2PF, England
[2] UCL Royal Free Hosp, Dept Plast & Reconstruct Surg, London NW3 2QG, England
关键词
purinergic receptors; ATP; P2X(7); melanoma; cancer; human;
D O I
10.1007/s00441-005-1149-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adenosine 5'-triphosphate is known to function as a potent extracellular messenger, producing its effects via a distinct family of cell surface receptors. Different receptor subtypes have been shown to modulate different cellular functions such as proliferation, differentiation and apoptosis. We have investigated the functional expression and apoptotic action of the P2X(7) receptor in human malignant melanoma tissue and cells. Incubation of cells with the potent P2X(7) receptor agonist 2'-3'-O-(4-benzoyl-benzoyl) adenosine 5'-triphosphate leads to a decrease in cell number, which is dose-dependent and reversible by the antagonist 1-N,O-bis-[5-isoquinoline-sulfonyl]-N-methyl-L-tyrosyl)-4-phenyl-piperazine. Synthesis of the P2X(7) receptor by these cells has been established by reverse transcriptase-polymerase chain reaction, immunohistochemistry, immunocytochemistry and cellular accumulation of the fluorescent DNA-binding dye YO-PRO-1. The P2X(7) receptors have been shown to mediate apoptotic actions of extracellular nucleotides and represent a novel target for melanoma therapy.
引用
收藏
页码:411 / 418
页数:8
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