P2Y receptor‐mediated Ca2+ signalling in cultured rat aortic smooth muscle cells
P2Y receptor‐mediated Ca2+ signalling in cultured rat aortic smooth muscle cells
复制标题
培养的大鼠主动脉平滑肌细胞中 P2Y 受体介导的 Ca2+ 信号传导
DOI:
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发表时间:
1999
影响因子:
7.3
通讯作者:
S. Wilson
中科院分区:
文献类型:
--
作者:
J. Pediani;J. McGrath;S. Wilson
ATP, UTP, ADP and ADP‐β‐S elicited Ca2+‐signals in cultured aortic smooth muscle cells although ADP, UDP and ADP‐β‐S gave ∼40% of the maximal response seen with ATP and UTP. Adenosine, AMP or α,β‐methylene‐ATP had no effect. These responses were attributed to P2Y2/4 and P2Y1 receptors, which we assumed could be selectively activated by UTP and ADP‐β‐S respectively. The response to UTP was reduced (∼50%) by pertussis toxin, whilst this toxin had no effect upon the response to ADP‐β‐S. This suggests P2Y2/4 receptors simultaneously couple to pertussis toxin‐sensitive and ‐resistant G proteins whilst P2Y1 receptors couple to only the toxin‐resistant proteins. Repeated stimulation with UTP or ADP‐β‐S caused desensitization which was potentiated by 12‐O‐tetradecanoyl phorbol‐13‐acetate (TPA) and attenuated by staurosporine. TPA completely abolished sensitivity to ADP‐β‐S but the response to UTP had a TPA‐resistant component. In pertussis toxin‐treated cells, however, TPA could completely abolish sensitivity to UTP and so the TPA‐resistant part of this response seems to be mediated by pertussis toxin‐sensitive G proteins. Loss of sensitivity to UTP did not occur when pertussis toxin‐treated cells were repeatedly stimulated with this nucleotide, suggesting that pertussis toxin‐sensitive G proteins mediate this effect. The toxin did not, however affect desensitization to ADP‐β‐S.
DOI:
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发表时间:
1996
期刊:
Molecular pharmacology.
影响因子:
--
作者:
Nicholas,RA;Watt,WC;Lazarowski,ER;Li,Q;Harden,K
通讯作者:
Harden,K
影响因子:
13.8
作者:
Fredholm, BB;Abbracchio, MP;Williams, M
通讯作者:
Williams, M
DOI:
10.1165/ajrcmb.12.1.7811468
发表时间:
1995
期刊:
American journal of respiratory cell and molecular biology.
影响因子:
--
作者:
Rice,WR;Burton,FM;Fiedeldey,DT
通讯作者:
Fiedeldey,DT