[HTML][HTML] Macrophage lipoprotein lipase promotes foam cell formation and atherosclerosis in vivo

VR Babaev, S Fazio, LA Gleaves… - The Journal of …, 1999 - Am Soc Clin Investig
VR Babaev, S Fazio, LA Gleaves, KJ Carter, CF Semenkovich, MRF Linton
The Journal of clinical investigation, 1999Am Soc Clin Investig
Expression of lipoprotein lipase (LPL) by the macrophage has been proposed to promote
foam cell formation and atherosclerosis, primarily on the basis of in vitro studies. LPL-
deficient mice might provide a model for testing the role of LPL secretion by the macrophage
in an in vivo system. Unfortunately, homozygous deficiency of LPL in the mouse is lethal
shortly after birth. Because the fetal liver is the major site of hematopoiesis in the developing
fetus, transplantation of C57BL/6 mice with LPL–/–fetal liver cells (FLCs) was used to …
Expression of lipoprotein lipase (LPL) by the macrophage has been proposed to promote foam cell formation and atherosclerosis, primarily on the basis of in vitro studies. LPL-deficient mice might provide a model for testing the role of LPL secretion by the macrophage in an in vivo system. Unfortunately, homozygous deficiency of LPL in the mouse is lethal shortly after birth. Because the fetal liver is the major site of hematopoiesis in the developing fetus, transplantation of C57BL/6 mice with LPL–/– fetal liver cells (FLCs) was used to investigate the physiologic role of macrophage LPL expression in vivo. Thirty-four female C57BL/6 mice were lethally irradiated and reconstituted with FLCs from day 14 LPL+/+, LPL+/–, and LPL–/– donors. No significant differences were detected in plasma levels of post-heparin LPL activity or in serum cholesterol or triglyceride levels between the 3 groups on either a chow diet or an atherogenic diet. After 19 weeks on the atherogenic diet, aortae were collected for quantitative analysis of the extent of aortic atherosclerosis. LPL expression was detected by immunocytochemistry and in situ hybridization in macrophages of aortic atherosclerotic lesions of LPL+/+→C57BL/6 and LPL+/–→C57BL/6 mice, but not in LPL–/–→C57BL/6 mice, whereas myocardial cells expressed LPL in all groups. The mean aortic lesion area was reduced by 55% in LPL–/–→C57BL/6 mice compared with LPL+/+→C57BL/6 mice and by 45% compared with LPL+/–→C57BL/6 mice, respectively. These data demonstrate in vivo that LPL expression by macrophages in the artery wall promotes foam cell formation and atherosclerosis.
J. Clin. Invest. 103:1697–1705 (1999).
The Journal of Clinical Investigation