Atherosclerosis and Lipoproteins |
From the Division of Biopharmaceutics (M.V.E., T.J.C.V.B.), Leiden/Amsterdam Center for Drug Research, Sylvius Laboratories, Leiden University, Leiden, The Netherlands; the Department of Biochemistry (R.Z., R.Z.), University of Graz, Graz, Austria; and the Department of Vascular Biology (P.H.E.G.), SmithKline Beecham Research and Development, Harlow, UK.
Correspondence to M. Van Eck, PhD, Division of Biopharmaceutics, Sylvius Laboratories, Leiden University, PO Box 9503, 2300 RA Leiden, The Netherlands. E-mail M.Eck{at}LACDR.LeidenUniv.nl
AbstractLipoprotein lipase (LPL)
synthesis by macrophages is upregulated in early atherogenesis,
implicating the possible involvement of LPL in plaque formation.
However, it is still unclear whether macrophage-derived LPL
displays a proatherosclerotic or an antiatherosclerotic role in
atherosclerotic lesion development. In this study, the role of
macrophage-derived LPL on lipid metabolism and
atherosclerosis was assessed in vivo by transplantation
of LPL-deficient (LPL-/-) and wild-type (LPL+/+) bone marrow into
C57BL/6 mice. Eight weeks after bone marrow transplantation
(BMT), serum cholesterol levels in LPL-/-
C57BL/6 mice
were reduced by 8% compared with those in LPL+/+
C57BL/6 mice
(P<0.05, n=16), whereas triglycerides were
increased by 33% (P<0.05, n=16). Feeding the mice a
high-cholesterol diet increased serum
cholesterol levels in LPL-/-
C57BL/6 and
LPL+/+
C57BL/6 mice 5-fold and 9-fold, respectively, resulting in a
difference of
50% (P<0.01) after 3 months on the diet.
No effects on triglyceride levels were observed under these
conditions. Furthermore, serum apolipoprotein E levels were reduced by
50% in the LPL-/-
C57BL/6 mice compared with controls under both
dietary conditions. After 3 months on a high-cholesterol
diet, the atherosclerotic lesion area in LPL-/-
C57BL/6 mice was
reduced by 52% compared with controls. It can be concluded that
macrophage-derived LPL plays a significant role in the
regulation of serum cholesterol, apolipoprotein E, and
atherogenesis, suggesting that specific blockade of macrophage
LPL production may be beneficial for decreasing atherosclerotic
lesion development.
Key Words: atherosclerosis transplantation blood cells enzymes lipids
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