A decreased expression of angiopoietin-like 3 is protective against atherosclerosis in apoE-deficient mice

• Published in: Journal of lipid research Vol. 44; no. 6; pp. 1216 - 1223
• Main Authors: Ando, Yosuke, Shimizugawa, Tetsuya, Takeshita, Shigehito, Ono, Mitsuru, Shimamura, Mitsuru, Koishi, Ryuta, Furukawa, Hidehiko
• Format: Journal Article
• Language: English
• Published: United States Elsevier 01-06-2003
• Subjects: Angiopoietin-like Proteins; Angiopoietins; Animals; Aortic Valve - pathology; apolipoprotein B; Apolipoproteins E - deficiency; Apolipoproteins E - genetics; Apolipoproteins E - metabolism; Arteriosclerosis - genetics; Arteriosclerosis - metabolism; Arteriosclerosis - pathology; Body Weight; Cholesterol, VLDL - blood; Cholesterol, VLDL - metabolism; Disease Models, Animal; hyperlipidemia; hypolipidemia; Intercellular Signaling Peptides and Proteins - biosynthesis; Intercellular Signaling Peptides and Proteins - genetics; Intercellular Signaling Peptides and Proteins - metabolism; Iodine Radioisotopes; Lipase - blood; Lipase - metabolism; Lipid Metabolism; Lipids - blood; lipoprotein lipase; Lipoprotein Lipase - blood; Lipoprotein Lipase - metabolism; Lipoproteins, VLDL - blood; Lipoproteins, VLDL - metabolism; Liver - enzymology; Liver - metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Postprandial Period; triglyceride-rich lipoproteins; Triglycerides - blood; Triglycerides - metabolism; Tritium; very low density lipoprotein
• ISSN: 0022-2275
• DOI: 10.1194/jlr.M300031-JLR200

KK/Snk mice (previously KK/San) possessing a recessive mutation (hypl) of the angiopoietin-like 3 (Angptl3) gene homozygously exhibit a marked reduction of VLDL due to the decreased Angptl3 expression. Recently, we proposed that Angptl3 is a new class of lipid metabolism modulator regulating VLDL triglyceride (TG) levels through the inhibition of lipoprotein lipase (LPL) activity. In this study, to elucidate the role of Angptl3 in atherogenesis, we investigated the effects of hypl mutation against hyperlipidemia and atherosclerosis in apolipoprotein E knockout (apoEKO) mice. ApoEKO mice with hypl mutation (apoEKO-hypl) exhibited a significant reduction of VLDL TG, VLDL cholesterol, and plasma apoB levels compared with apoEKO mice. Hepatic VLDL TG secretion was comparable between both apoE-deficient mice. Turnover studies revealed that the clearance of both [3H]TG-labeled and 125I-labeled VLDL was significantly enhanced in apoEKO-hypl mice. Postprandial plasma TG levels also decreased in apoEKO-hypl mice. Both LPL and hepatic lipase activities in the postheparin plasma increased significantly in apoEKO-hypl mice, explaining the enhanced lipid metabolism. Furthermore, apoEKO-hypl mice developed 3-fold smaller atherogenic lesions in the aortic sinus compared with apoEKO mice. Taken together, the reduction of Angptl3 expression is protective against hyperlipidemia and atherosclerosis, even in the absence of apoE, owing to the enhanced catabolism and clearance of TG-rich lipoproteins.