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Dictyostelium Uses Ether-linked Inositol Phospholipids for Intracellular Signalling

Overview
Journal EMBO J
Date 2014 Sep 3
PMID 25180230
Citations 33
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Abstract

Inositol phospholipids are critical regulators of membrane biology throughout eukaryotes. The general principle by which they perform these roles is conserved across species and involves binding of differentially phosphorylated inositol head groups to specific protein domains. This interaction serves to both recruit and regulate the activity of several different classes of protein which act on membrane surfaces. In mammalian cells, these phosphorylated inositol head groups are predominantly borne by a C38:4 diacylglycerol backbone. We show here that the inositol phospholipids of Dictyostelium are different, being highly enriched in an unusual C34:1e lipid backbone, 1-hexadecyl-2-(11Z-octadecenoyl)-sn-glycero-3-phospho-(1'-myo-inositol), in which the sn-1 position contains an ether-linked C16:0 chain; they are thus plasmanylinositols. These plasmanylinositols respond acutely to stimulation of cells with chemoattractants, and their levels are regulated by PIPKs, PI3Ks and PTEN. In mammals and now in Dictyostelium, the hydrocarbon chains of inositol phospholipids are a highly selected subset of those available to other phospholipids, suggesting that different molecular selectors are at play in these organisms but serve a common, evolutionarily conserved purpose.

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References
1.
Montrucchio G, Alloatti G, Camussi G . Role of platelet-activating factor in cardiovascular pathophysiology. Physiol Rev. 2000; 80(4):1669-99. DOI: 10.1152/physrev.2000.80.4.1669. View

2.
Burman C, Ktistakis N . Regulation of autophagy by phosphatidylinositol 3-phosphate. FEBS Lett. 2010; 584(7):1302-12. DOI: 10.1016/j.febslet.2010.01.011. View

3.
Hoeller O, Kay R . Chemotaxis in the absence of PIP3 gradients. Curr Biol. 2007; 17(9):813-7. DOI: 10.1016/j.cub.2007.04.004. View

4.
Zoeller R, Lake A, Nagan N, Gaposchkin D, Legner M, Lieberthal W . Plasmalogens as endogenous antioxidants: somatic cell mutants reveal the importance of the vinyl ether. Biochem J. 1999; 338 ( Pt 3):769-76. PMC: 1220115. View

5.
Iijima M, Devreotes P . Tumor suppressor PTEN mediates sensing of chemoattractant gradients. Cell. 2002; 109(5):599-610. DOI: 10.1016/s0092-8674(02)00745-6. View