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GDE2 is essential for neuronal survival in the postnatal mammalian spinal cord.

Mol Neurodegener. 2017 Jan 19;12(1):8
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摘要


BACKGROUND:Glycerophosphodiester phosphodiesterase 2 (GDE2) is a six-transmembrane protein that cleaves glycosylphosphatidylinositol (GPI) anchors to regulate GPI-anchored protein activity at the cell surface. In the developing spinal cord, GDE2 utilizes its enzymatic function to regulate the production of specific classes of motor neurons and interneurons; however, GDE2's roles beyond embryonic neurogenesis have yet to be defined. METHOD:mouse model of familial Amyotrophic Lateral Sclerosis that shows robust motor neuron degeneration. RESULTS:mice. CONCLUSIONS:This study identifies a novel function for GDE2 in neuronal survival and implicates deregulated GPI-anchored protein activity in pathways mediating neurodegeneration. These findings provide new molecular insight for neuropathologies found in multiple disease settings, and raise the possibility of GDE2 hypofunctionality as a component of neurodegenerative disease.

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