4.6 Article

Apolipoprotein B in cholesterol-containing drusen and basal deposits of human eyes with age-related maculopathy

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 162, Issue 2, Pages 413-425

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S0002-9440(10)63836-9

Keywords

-

Categories

Funding

  1. NEI NIH HHS [EY 06109, T32 EY007033, R01 EY013258, EY 13258, R01 EY006109, T32-EY07033] Funding Source: Medline

Ask authors/readers for more resources

Lipids accumulate in Bruch's membrane (BrM), a specialized vascular intima of the eye, and in extracellular lesions associated with aging and age-related maculopathy (ARM). We tested the hypothesis that ARM and atherosclerotic cardiovascular disease share molecules and mechanisms pertaining to extracellular lipid accumulation by localizing cholesterol and apolipoprotein B (apo B) in BrM, basal deposits, and drusen. Human donor eyes were preserved < 4 hours postmortem and cryosectioned. Sections were stained with traditional lipid stains and filipin for esterified and unesterifted cholesterol or probed with antibodies to apo B, apo E, and apo C-III. Normal adult retinal pigment epithelium (RPE) was subjected to RT-PCR and Western blot analysis for apolipoprotein mRNA and protein. Esterified and unesterified cholesterol was present in all drusen and basal deposits of ARM and normal eyes. Both apo B and apo E but not apo C-III were found in BrM, drusen, and basal deposits. Fewer macular drusen were stained by traditional lipid stains and apolipoprotein antibodies than peripheral drusen. RPE contained apo B and apo E mRNA and protein. Finding cholesterol and apo B in sub-RPE deposits links ARM with important molecules and mechanisms in atherosclerosis initiation and progression. The combination of apo B mRNA and protein in RPE raises the possibility that intraocular assembly of apo B-containing lipoproteins is a pathway involved in forming cholesterol-enriched lesions in ARM.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available