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Wiley InterScience

Journal of Neurochemistry

Journal of Neurochemistry

Volume 70 Issue 5, Pages 2070 - 2081

Published Online: 13 Nov 2002

Journal compilation © 2010 International Society for Neurochemistry



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Nascent Astrocyte Particles Differ from Lipoproteins in CSF
M. J. LaDu, S. M. Gilligan, J. R. Lukens, V. G. Cabana, C. A. Reardon, *L. J. Van Eldik, and D. M. Holtzman
  Department of Pathology, University of Chicago, and   *Department of Cell and Molecular Biology and Northwestern Drug Discovery Program, Northwestern University School of Medicine, Chicago, Illinois; and   Department of Neurology, Molecular Biology, and Pharmacology, and Center for the Study of Nervous System Injury, Washington University School of Medicine, St. Louis, Missouri, U.S.A.
Address correspondence and reprint requests to Dr. D. M. Holtzman at Washington University School of Medicine, Department of Neurology, CSNSI, 660 S. Euclid Ave., Box 8111, St. Louis, MO 63110, U.S.A.
Copyright Blackwell Science Inc
KEYWORDS
Apolipoprotein E • Apolipoprotein J • Apolipoprotein AI • Alzheimer's disease • Cholesterol

ABSTRACT

Abstract: Little is known about lipid transport and metabolism in the brain. As a further step toward understanding the origin and function of CNS lipoproteins, we have characterized by size and density fractionation lipoprotein particles from human CSF and primary cultures of rat astrocytes. The fractions were analyzed for esterified and free cholesterol, triglyceride, phospholipid, albumin, and apolipoproteins (apo) E, AI, AII, and J. As determined by lipid and apolipoprotein profiles, gel electrophoresis, and electron microscopy, nascent astrocyte particles contain little core lipid, are primarily discoidal in shape, and contain apoE and apoJ. In contrast, CSF lipoproteins are the size and density of plasma high-density lipoprotein, contain the core lipid, esterified cholesterol, and are spherical. CSF lipoproteins were heterogeneous in apolipoprotein content with apoE, the most abundant apolipoprotein, localized to the largest particles, apoAI and apoAII localized to progressively smaller particles, and apoJ distributed relatively evenly across particle size. There was substantial loss of protein from both CSF and astrocyte particles after density centrifugation compared with gel-filtration chromatography. The differences between lipoproteins secreted by astrocytes and present in CSF suggest that in addition to delivery of their constituents to cells, lipoprotein particles secreted within the brain by astrocytes may have the potential to participate in cholesterol clearance, developing a core of esterified cholesterol before reaching the CSF. Study of the functional properties of both astrocyte-secreted and CSF lipoproteins isolated by techniques that preserve native particle structure may also provide insight into the function of apoE in the pathophysiology of specific neurological diseases such as Alzheimer's disease.


Received September 18, 1997; revised manuscript received November 25, 1997; accepted November 27, 1997.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1046/j.1471-4159.1998.70052070.x About DOI

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