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Immunocytochemical techniques reveal multiple, distinct cellular pools of PtdIns4P and PtdIns(4,5)P2
被引:229
作者:
Hammond, Gerald R. V.
[1
]
Schiavo, Giampietro
[2
]
Irvine, Robin F.
[1
]
机构:
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
[2] Lincolns Inn Fields Labs, Canc Res UK London Res Inst, Mol Neuropathobiol Lab, London WC2A 3PX, England
基金:
英国惠康基金;
关键词:
Golgi;
immunofluorescence;
phosphoinositides;
plasma membrane;
PtdIns(4,5)P-2;
PtdIns4P;
PLECKSTRIN HOMOLOGY DOMAIN;
PHOSPHATIDYLINOSITOL 4-KINASE ISOFORMS;
INOSITOL-POLYPHOSPHATE;
5-PHOSPHATASE;
PLASMA-MEMBRANE;
ENDOPLASMIC-RETICULUM;
BINDING-PROTEIN;
HIGH-AFFINITY;
FIXED CELLS;
GOLGI;
LOCALIZATION;
D O I:
10.1042/BJ20090428
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:
PtdIns4P is the major precursor for the synthesis of the multifunctional plasma membrane lipid, PtdIns(4,5)P-2. Yet PtdIns4P also functions as a regulatory lipid in its own right, particularly at the Golgi apparatus. In the present study we define specific conditions that enable preservation of several organellar membranes for the immunocytochemical detection of PtdIns4P. We report distinct pools of this lipid in both Golgi and plasma membranes, which are synthesized by different PI4K (phosphatidylinositol 4-kinase) activities, and also the presence of PtdIns4P in cytoplasmic vesicles, which are not readily identifiable as PI4K containing trafficking intermediates. In addition, we present evidence that the majority of PtdIns4P resides in the plasma membrane, where it is metabolically distinct from the steady-state plasma membrane pool of PtdIns(4,5)P-2.
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页码:23 / 35
页数:13
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