Journal article
Ndfip1 regulates nuclear Pten import in vivo to promote neuronal survival following cerebral ischemia
J Howitt, J Lackovic, LH Low, A Naguib, A Macintyre, CP Goh, JK Callaway, V Hammond, T Thomas, M Dixon, U Putz, J Silke, P Bartlett, B Yang, S Kumar, LC Trotman, SS Tan
Journal of Cell Biology | Published : 2012
Abstract
PTEN (phosphatase and tensin homologue deleted on chromosome TEN) is the major negative regulator of phosphatidylinositol 3-kinase signaling and has cell-specific functions including tumor suppression. Nuclear localization of PTEN is vital for tumor suppression; however, outside of cancer, the molecular and physiological events driving PTEN nuclear entry are unknown. In this paper, we demonstrate that cytoplasmic Pten was translocated into the nuclei of neurons after cerebral ischemia in mice. Critically, this transport event was dependent on a surge in the Nedd4 family-interacting protein 1 (Ndfip1), as neurons in Ndfip1-deficient mice failed to import Pten. Ndfip1 binds to Pten, resulting ..
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Awarded by National Cancer Institute
Funding Acknowledgements
This work was supported by the National Health and Medical Research Council and the Victorian government through the Operational Infrastructure Support Program.