
pmid: 25680866
Phosphoinositide (PIP) lipids regulate many aspects of cell function in the nervous system including receptor signalling, secretion, endocytosis, migration and survival. Levels of PIPs such as PI4P, PI(4,5)P2 and PI(3,4,5)P3 are normally tightly regulated by phosphoinositide kinases and phosphatases. Deregulation of these biochemical pathways leads to lipid imbalances, usually on intracellular endosomal membranes, and these changes have been linked to a number of major neurological diseases including Alzheimer's, Parkinson's, epilepsy, stroke, cancer and a range of rarer inherited disorders including brain overgrowth syndromes, Charcot-Marie-Tooth neuropathies and neurodevelopmental conditions such as Lowe's syndrome. This article analyses recent progress in this area and explains how PIP lipids are involved, to varying degrees, in almost every class of neurological disease. This article is part of a Special Issue entitled Brain Lipids.
Epilepsy, Membrane, PTEN Phosphohydrolase, Brain, Gene Expression, Parkinson Disease, Lipid, Phosphatidylinositols, Stroke, Phosphotransferases (Alcohol Group Acceptor), Oculocerebrorenal Syndrome, Alzheimer Disease, Charcot-Marie-Tooth Disease, Mutation, Endosome, Humans, Disease, Phosphatidylinositol, Signal Transduction
Epilepsy, Membrane, PTEN Phosphohydrolase, Brain, Gene Expression, Parkinson Disease, Lipid, Phosphatidylinositols, Stroke, Phosphotransferases (Alcohol Group Acceptor), Oculocerebrorenal Syndrome, Alzheimer Disease, Charcot-Marie-Tooth Disease, Mutation, Endosome, Humans, Disease, Phosphatidylinositol, Signal Transduction
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