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1.
Invest Ophthalmol Vis Sci ; 50(8): 3931-42, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19420333

ABSTRACT

PURPOSE: To evaluate functional and ultrastructural changes in the retina of scavenger receptor B1 (SR-BI) knockout (KO) mice consuming a high fat cholate (HFC) diet. METHODS: Three-month-old male KO and wild-type (WT) mice were fed an HFC diet for 30 weeks. After diet supplementation, plasma cholesterol levels and electroretinograms were analyzed. Neutral lipids were detected with oil red O, and immunohistochemistry was performed on cryostat ocular tissue sections. The retina, Bruch's membrane (BM), retinal pigment epithelium (RPE), and choriocapillaris (CC) were analyzed by transmission electron microscopy. RESULTS: Using the WT for reference, ultrastructural changes were recorded in HFC-fed SR-BI KO mice, including lipid inclusions, a patchy disorganization of the photoreceptor outer segment (POS) and the outer nuclear layer (ONL), and BM thickening with sparse sub-RPE deposits. Within the CC, there was abnormal disorganization of collagen fibers localized in ectopic sites with sparse and large vacuolization associated with infiltration of macrophages in the subretinal space, reflecting local inflammation. These lesions were associated with electroretinographic abnormalities, particularly increasing implicit time in a- and b-wave scotopic responses. Abnormal vascular endothelial growth factor (VEGF) staining was detected in the outer nuclear layer. CONCLUSIONS: HFC-fed SR-BI KO mice thus presented sub-RPE lipid-rich deposits and functional and morphologic alterations similar to some features observed in dry AMD. The findings lend further support to the hypothesis that atherosclerosis causes retinal and subretinal damage that increases susceptibility to some forms of AMD.


Subject(s)
Coronary Artery Disease/pathology , Diet, Atherogenic , Hypercholesterolemia/pathology , Macular Degeneration/pathology , Retina/physiology , Retina/ultrastructure , Scavenger Receptors, Class B/physiology , Animals , Bruch Membrane/ultrastructure , Cholates/administration & dosage , Cholesterol/blood , Choroid/blood supply , Coronary Artery Disease/etiology , Coronary Artery Disease/metabolism , Electroretinography , Hypercholesterolemia/etiology , Hypercholesterolemia/metabolism , Macular Degeneration/etiology , Macular Degeneration/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Phenotype , Retinal Pigment Epithelium/ultrastructure , Vascular Endothelial Growth Factor A/metabolism
2.
C R Biol ; 326(9): 841-51, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14694755

ABSTRACT

The class-B type-I scavenger receptor (SR-BI) plays a key role in cholesterol homeostasis; it mediates the selective uptake of lipoprotein cholesterol to steroidogenic tissues. We show by RT-PCR, western blot, in situ hybridization and immunohistochemistry analysis that SR-BI is highly expressed in different neuro-retinal and non-neuronal cells types on rat eye. Immunohistochemistry of the steroidogenic acute regulatory protein (StAR) involved in neurosteroid production showed the same expression pattern than SR-BI in rat eye. Our results may suggest a key role of these genes in the ocular cholesterol metabolism for membranes biosynthesis and neurosteroidogenesis.


Subject(s)
Ocular Physiological Phenomena , Phosphoproteins/genetics , Receptors, Immunologic/genetics , Animals , Brain/physiology , CD36 Antigens , Gene Expression Regulation , In Situ Hybridization , RNA, Messenger/genetics , Rats , Rats, Inbred Strains , Rats, Mutant Strains , Receptors, Scavenger , Reverse Transcriptase Polymerase Chain Reaction , Scavenger Receptors, Class B , Transcription, Genetic
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