Endogenous extracellular purine nucleotides redirect α2-adrenoceptor signaling

被引:15
作者
Åkerman, KEO [1 ]
Näsman, J [1 ]
Lund, PE [1 ]
Shariatmadari, R [1 ]
Kukkonen, JP [1 ]
机构
[1] Univ Uppsala, Ctr Biomed, Dept Physiol, S-75123 Uppsala, Sweden
基金
英国医学研究理事会;
关键词
alpha(2)-adrenoceptor; P-2Y-receptor; apyrase; suramin; calcium; fura-2;
D O I
10.1016/S0014-5793(98)00664-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many receptors coupled to inhibitory G(o)/G(i)-type G proteins often also produce stimulatory signals like Ca2+ mobilisation. When expressed in CHO cells the alpha(2)-adrenoceptor subtypes alpha(2A), alpha(2B) and alpha(2C) mobilised Ca2+, These responses were strongly reduced by the P-2y-purinoceptor antagonist suramin, A large proportion of the total pool of purine nucleotides was found extracellularly. Removal of extracellular nucleotides with apyrase or by constant perfusion had a similar effect as suramin. These treatments did not affect the adrenoceptor-mediated inhibition of cAMP production. This indicates that cells may be primed or their signaling pathways redirected towards Ca2+ mobilisation by 'autocrine' release of nucleotides. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:209 / 212
页数:4
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