Target-specific PIP2 signalling:: how might it work?

被引:96
作者
Gamper, Nikita [1 ]
Shapiro, Mark S.
机构
[1] Univ Leeds, Fac Biol Sci, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Texas, Hlth Sci Ctr, Dept Physiol, San Antonio, TX 78229 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2007年 / 582卷 / 03期
基金
英国惠康基金;
关键词
D O I
10.1113/jphysiol.2007.132787
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Phosphatidylinositol 4,5-bisphosphate (PIP2)-mediated signalling is a new and rapidly developing area in the field of cellular signal transduction. With the extensive and growing list Of PIP2-sensitive membrane proteins (many of which are ion channels and transporters) and multiple signals affecting plasma membrane PIP2 levels, the question arises as to the cellular mechanisms that confer specificity to PIP2-mediated signalling. In this review we critically consider two major hypotheses for such possible mechanisms: (i) clustering of PIP2 in membrane microdomains with restricted lateral diffusion, a hypothesis providing a mechanism for spatial segregation Of PIP2 signals and (ii) receptor-specific buffering of the global plasma membrane PIP2 pool via Ca2+-mediated stimulation of PIP2 synthesis or release, a concept allowing for receptor-specific signalling with free lateral diffusion Of PIP2. We also discuss several other technical and conceptual intricacies Of PIP2-mediated signalling.
引用
收藏
页码:967 / 975
页数:9
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