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24S-hydroxycholesterol and cholesterol-24S-hydroxylase (CYP46A1) in the retina: from cholesterol homeostasis to pathophysiology of glaucoma
Authors:Fourgeux Cynthia  Bron Alain  Acar Niyazi  Creuzot-Garcher Catherine  Bretillon Lionel
Institution:aEye & Nutrition Research Group, Centre des Sciences du Goût et de l’Alimentation, UMR 1324 INRA, 6265 CNRS, University of Burgundy, Centre de recherche INRA, 17 rue Sully, F-21000 Dijon, France;bDepartment of Ophthalmology, University Hospital, 3 rue du Faubourg Raines, F-21000 Dijon, France
Abstract:Free cholesterol is the predominant form of cholesterol in the neural retina. The vertebrate neural retina exhibits its own capacity to synthesize cholesterol and meets its demand also by taking it from the circulation. Defects in cholesterol synthesis and trafficking in the neural retina has detrimental consequences on its structure and function, highlighting the crucial importance of maintaining cholesterol homeostasis in the retina. Our purpose was to give a review on the functioning of the retina, the role of cholesterol and cholesterol metabolism therein, with special emphasis on cholesterol-24S-hydroxylase (CYP46A1). Similar to the brain, the retina expresses cholesterol-24S-hydroxylase (CYP46A1) and is enriched in its metabolic product, 24S-hydroxycholesterol. We recently published that one single nucleotide polymorphism in CYP46A1 gene, designated as rs754203, was a risk factor for glaucoma. Glaucoma is the second leading cause of blindness worldwide, affecting more than 60 million people. Glaucoma is characterized by the loss of retinal ganglion cells, which show high CYP46A1 expression. These data suggest the potential involvement of CYP46A1 and 24S-hydroxycholesterol in the pathophysiology of glaucoma.
Keywords:Abbreviations: AMD  age-related macular degeneration  DHA  docosahexaenoic acid  RGC  retinal ganglion cells  RPE  retinal pigment epithelium  SLOS  Smith-Lemli-Opitz syndrome
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