Atherosclerosis and Lipoproteins |
From the Division of Biopharmaceutics, Leiden/Amsterdam Center for Drug Research (M.V.E., N.H., Th.J.C.), and the Department of Human Genetics (M.P.J.D.W., M.H.H.), Leiden University Medical Center, Sylvius Laboratories, Leiden University (The Netherlands); TNO Prevention and Health, Gaubius Laboratories (L.M.H.), Leiden, The Netherlands; and SmithKline Beecham Pharmaceuticals, (P.H.E.G.) NFSP(N), Harlow, Essex, UK.
Correspondence to M. Van Eck, MSc, Division of Biopharmaceutics, Sylvius Laboratories, Leiden University, PO Box 9503, 2300 RA Leiden, The Netherlands. E-mail M.Eck{at}LACDR.LeidenUniv.nl
AbstractIn the
arterial wall, scavenger receptor class A (SRA) is
implicated in pathological lipid deposition. In contrast, in the liver,
SRA is suggested to remove modified lipoproteins from the circulation,
thereby protecting the body from their pathological action. The role of
SRA on bone marrowderived cells in lipid metabolism and
atherogenesis was assessed in vivo by transplantation of bone marrow
cells overexpressing human SRA (MSR1) to apoE-deficient mice. In vitro
studies with peritoneal macrophages from the transplanted mice
showed that macrophage scavenger receptor function, as measured
by cell association and degradation studies with acetylated
LDL, was
3-fold increased on overexpression of MSR1 in bone
marrowderived cells as compared with control mice. Despite the
increased macrophage scavenger receptor function in vitro, no
significant effect of MSR1 overexpression in bone marrowderived cells
on the in vivo atherosclerotic lesion development was found. In
addition to arterial wall macrophages, liver
sinusoidal Kupffer cells also overexpress MSR1 after bone marrow
transplantation, which may scavenge atherogenic particles more
efficiently from the blood compartment. Introduction of bone marrow
cells overexpressing human MSR1 in apoE-deficient mice induced a
significant reduction in serum cholesterol levels of
20% (P<0.001, 2-way ANOVA) as the result of a
decrease in VLDL cholesterol. It is suggested that the
reduction in VLDL cholesterol levels is due to increased
clearance of modified lipoproteins by the overexpressed MSR1 in Kupffer
cells of the liver, thereby protecting the arterial wall
against the proatherogenic action of modified lipoproteins.
Key Words: scavenger receptor atherosclerosis hyperlipidemia macrophages bone marrow transplantation
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