Faculty Opinions recommendation of An electrostatic switch displaces phosphatidylinositol phosphate kinases from the membrane during phagocytosis.

Author(s):  
Christopher Janetopoulos
2016 ◽  
Vol 110 (3) ◽  
pp. 573a
Author(s):  
Fiona B. Naughton ◽  
Antreas C. Kalli ◽  
Mark S.P. Sansom

1987 ◽  
Vol 248 (3) ◽  
pp. 765-770 ◽  
Author(s):  
L Cocco ◽  
R S Gilmour ◽  
A Ognibene ◽  
A J Letcher ◽  
F A Manzoli ◽  
...  

Previous work demonstrated the existence of phosphatidylinositol kinase and phosphatidylinositol phosphate kinase in rat liver nuclei, with the suggestion that these activities are in the nuclear membrane [Smith & Wells (1983) J. Biol. Chem. 258, 9368-9373]. Here we show that highly purified nuclei from Friend cells, washed free of nuclear membrane by Triton, can incorporate radiolabel from [gamma-32P]ATP into phosphatidic acid, phosphatidylinositol phosphate and phosphatidylinositol 4,5-bisphosphate. The degree of radiolabelling of phosphatidylinositol bisphosphate is highly dependent on the state of differentiation of the cells, being barely detectable in growing cells and much greater after dimethyl sulphoxide-induced differentiation; this difference is mostly due to different amounts of phosphatidylinositol phosphate in the isolated nuclei. We suggest that polyphosphoinositides are made inside the nucleus and that they have a role in chromatin function; either the phospholipids themselves play a role, or there is a possibility of intranuclear signalling by inositide-derived molecules.


2008 ◽  
Vol 295 (5) ◽  
pp. F1422-F1430 ◽  
Author(s):  
Jonathan H. Clarke ◽  
Piers C. Emson ◽  
Robin F. Irvine

PIP4Ks (type II phosphatidylinositol 4-phosphate kinases) are phosphatidylinositol 5-phosphate (PtdIns5P) 4-kinases, believed primarily to regulate cellular PtdIns5P levels. In this study, we investigated the expression, localization, and associated biological activity of the least-studied PIP4K isoform, PIP4Kγ. Quantitative RT-PCR and in situ hybridization revealed that compared with PIP4Kα and PIP4Kβ, PIP4Kγ is expressed at exceptionally high levels in the kidney, especially the cortex and outer medulla. A specific antibody was raised to PIP4Kγ, and immunohistochemistry with this and with antibodies to specific kidney cell markers showed a restricted expression, primarily distributed in epithelial cells in the thick ascending limb and in the intercalated cells of the collecting duct. In these cells, PIP4Kγ had a vesicular appearance, and transfection of kidney cell lines revealed a partial Golgi localization (primarily the matrix of the cis-Golgi) with an additional presence in an unidentified vesicular compartment. In contrast to PIP4Kα, bacterially expressed recombinant PIP4Kγ was completely inactive but did have the ability to associate with active PIP4Kα in vitro. Overall our data suggest that PIP4Kγ may have a function in the regulation of vesicular transport in specialized kidney epithelial cells.


2019 ◽  
Vol 133 (2) ◽  
pp. jcs233254 ◽  
Author(s):  
Lizbeth de la Cruz ◽  
Alexis Traynor-Kaplan ◽  
Oscar Vivas ◽  
Bertil Hille ◽  
Jill B. Jensen

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