共 49 条
Tailoring cAMP-signalling responses through isoform multiplicity
被引:389
作者:

Houslay, MD
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Pharmacology Group, Inst. of Life and Biomed. Sciences, University of Glasgow, Glasgow

Milligan, G
论文数: 0 引用数: 0
h-index: 0
机构: Molecular Pharmacology Group, Inst. of Life and Biomed. Sciences, University of Glasgow, Glasgow
机构:
[1] Molecular Pharmacology Group, Inst. of Life and Biomed. Sciences, University of Glasgow, Glasgow
基金:
英国惠康基金;
关键词:
D O I:
10.1016/S0968-0004(97)01050-5
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:
Multiple forms of cAMP phosphodiesterases (PDE), adenylate cyclase and protein kinase A (PKA) allow cells to tailor the responsiveness of the cAMP-signalling system and to allow for its dynamic adjustment. Multiple forms of these enzymes confer spatial anti temporal characteristics on cAMP signalling so as to affect compartmentalised responses within a single cell type. The ability to breach the PKA activation threshold can depend upon either or both the activation of adenylate cyclase and inhibition of specific PDE isoforms.
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收藏
页码:217 / 224
页数:8
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