PI4P and PI(4,5)P2 Are Essential But Independent Lipid Determinants of Membrane Identity

被引:350
作者
Hammond, Gerald R. V. [1 ,3 ]
Fischer, Michael J. [1 ]
Anderson, Karen E. [2 ]
Holdich, Jon [1 ]
Koteci, Ardita [1 ]
Balla, Tamas [3 ]
Irvine, Robin F. [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
[2] Babraham Inst, Inositide Lab, Cambridge CB22 3AT, England
[3] NICHHD, Sect Mol Signal Transduct, Program Dev Neurosci, NIH, Bethesda, MD 20892 USA
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; PLASMA-MEMBRANE; LIVING CELLS; K+ CHANNEL; PHOSPHOINOSITIDES; DOMAINS; POOLS; ACTIVATION; PROTEINS; MULTIPLE;
D O I
10.1126/science.1222483
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The quantitatively minor phospholipid phosphatidylinositol (4,5)-bisphosphate [PI(4,5)P-2] fulfills many cellular functions in the plasma membrane (PM), whereas its synthetic precursor, phosphatidylinositol 4-phosphate (PI4P), has no assigned PM roles apart from PI(4,5)P-2 synthesis. We used a combination of pharmacological and chemical genetic approaches to probe the function of PM PI4P, most of which was not required for the synthesis or functions of PI(4,5)P-2. However, depletion of both lipids was required to prevent PM targeting of proteins that interact with acidic lipids or activation of the transient receptor potential vanilloid 1 cation channel. Therefore, PI4P contributes to the pool of polyanionic lipids that define plasma membrane identity and to some functions previously attributed specifically to PI(4,5)P-2, which may be fulfilled by a more general polyanionic lipid requirement.
引用
收藏
页码:727 / 730
页数:4
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