Abstract
The epsilon 4 allele of apolipoprotein E (apoE) is a major risk factor for Alzheimer disease, suggesting that apoE may directly influence neurons in the aging brain. Recent data suggest that apoE-containing lipoproteins can influence neurite outgrowth in an isoform-specific fashion. The neuronal mediators of apoE effects have not been clarified. We show here that in a central nervous system-derived neuronal cell line, apoE3 but not apoE4 increases neurite extension. The effect of apoE3 was blocked at low nanomolar concentrations by purified 39-kDa protein that regulates ligand binding to the low density lipoprotein receptor-related protein (LRP). Anti-LRP antibody also completely abolished the neurite-promoting effect of apoE3. Understanding isoform-specific cell biological processes mediated by apoE-LRP interactions in central nervous system neurons may provide insight into Alzheimer disease pathogenesis.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Apolipoprotein E3
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Apolipoproteins E / metabolism*
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Carbocyanines
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Cell Line
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Cross-Linking Reagents
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Fluorescent Antibody Technique, Indirect
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Fluorescent Dyes
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Hypothalamus / cytology
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Hypothalamus / physiology*
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Low Density Lipoprotein Receptor-Related Protein-1
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Microscopy, Confocal
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Microscopy, Fluorescence
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Neurites / physiology*
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Neurites / ultrastructure
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Neurons / cytology
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Neurons / physiology
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Receptors, Immunologic / genetics
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Receptors, Immunologic / immunology
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Receptors, Immunologic / metabolism*
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Receptors, LDL / metabolism*
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Recombinant Proteins / immunology
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Recombinant Proteins / metabolism
Substances
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Apolipoprotein E3
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Apolipoproteins E
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Carbocyanines
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Cross-Linking Reagents
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Fluorescent Dyes
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Low Density Lipoprotein Receptor-Related Protein-1
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Receptors, Immunologic
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Receptors, LDL
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Recombinant Proteins
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3,3'-dioctadecylindocarbocyanine