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First published online December 11, 2006
doi: 10.1242/10.1242/jcs.000133


Journal of Cell Science 119, 5160-5168 (2006)
Published by The Company of Biologists 2006
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Research Article

Localization of agonist-sensitive PtdIns(3,4,5)P3 reveals a nuclear pool that is insensitive to PTEN expression

Yvonne Lindsay1, David McCoull1, Lindsay Davidson1, Nick R. Leslie1, Alison Fairservice1, Alex Gray1, John Lucocq2 and C. Peter Downes1,*

1 Division of Molecular Physiology, College of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK
2 Division of Cell Biology and Immunology, College of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK

* Author for correspondence (c.p.downes{at}dundee.ac.uk)

Accepted 22 October 2006

Phosphatidylinositol (3,4,5) trisphosphate [PtdIns(3,4,5)P3] is a lipid second messenger, produced by Type I phosphoinositide 3-kinases (PI 3-kinases), which mediates intracellular responses to many growth factors. Although PI 3-kinases are implicated in events at both the plasma membrane and intracellular sites, including the nucleus, direct evidence for the occurrence of PtdIns(3,4,5)P3 at non-plasma membrane locations is limited. We made use of the pleckstrin homology (PH) domain of general receptor for phosphoinositides (Grp1) to detect PtdIns(3,4,5)P3 in an on-section labeling approach by quantitative immunogold electron microscopy. Swiss 3T3 cells contained low levels of PtdIns(3,4,5)P3 that increased up to 15-fold upon stimulation with platelet-derived growth factor (PDGF). The signal was sensitive to PI 3-kinase inhibitors and present mainly at plasma membranes, including lamellipodia, and in a surprisingly large pool within the nuclear matrix. Comparatively little labeling was observed in endomembranes. A similar distribution of PtdIns(3,4,5)P3 was observed in U87MG cells, which lack the PtdIns(3,4,5)P3 phosphatase, PTEN. Re-expression of PTEN into U87MG cells ablated plasma membrane PtdIns(3,4,5)P3, but not the nuclear pool of this lipid even when PTEN was targeted to nuclei. These data have important implications for the versatility of PI 3-kinase signaling and for the proposed functions of PTEN in the nucleus.

Key words: Phosphoinositide 3-kinase, Phosphatidylinositol trisphosphate, Nucleus, Phosphatase, PTEN, Electron microscopy


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