Unique lipoproteins secreted by primary astrocytes from wild type, apoE (-/-), and human apoE transgenic mice

Anne M. Fagan, David M. Holtzman, Gregory Munson, Tanya Mathur, Danielle Schneider, Louis K. Chang, Godfrey S. Getz, Catherine A. Reardon, John Lukens, Javeed A. Shah, Mary Jo LaDu

Research output: Contribution to journalArticlepeer-review

178 Scopus citations


Composition of central nervous system lipoproteins affects the metabolism of lipoprotein constituents within the brain. The ε4 allele of apolipoprotein E (apoE) is a risk factor for Alzheimer's disease via an unknown mechanism(s). As glia are the primary central nervous system cell type that synthesize apoE, we characterized lipoproteins secreted by astrocytes from wild type (WT), apoE (-/-), and apoE transgenic mice expressing human apoE3 or apoE4 in a mouse apoE (-/-) background. Nondenaturing size exclusion chromatography demonstrates that WT, apoE3, and apoE4 astrocytes secrete particles the size of plasma high density lipoprotein (HDL) composed of phospholipid, free cholesterol, and protein, primarily apoE and apoJ. However, the lipid:apoE ratio of particles containing human apoE is significantly lower than WT. ApoE localizes across HDL-like particle sizes. ApoJ localizes to the smallest HDL-like particles. ApoE (-/-) astrocytes secrete little phospholipid or free cholesterol despite comparable apoJ expression, suggesting that apoE is required for normal secretion of astrocyte lipoproteins. Further, particles were not detected in apoE (-/-) samples by electron microscopy. Nondenaturing immunoprecipitation experiments indicate that apoE and apoJ reside predominantly on distinct particles. These studies suggest that apoE expression influences the unique structure of astrocyte lipoproteins, a process further modified by apoE species.

Original languageEnglish
Pages (from-to)30001-30007
Number of pages7
JournalJournal of Biological Chemistry
Issue number42
StatePublished - Oct 15 1999


Dive into the research topics of 'Unique lipoproteins secreted by primary astrocytes from wild type, apoE (-/-), and human apoE transgenic mice'. Together they form a unique fingerprint.

Cite this