Acute elevation of plasma PLTP activity strongly increases pre-existing atherosclerosis
Arteriosclerosis, Thrombosis, and Vascular Biology , Volume 28 - Issue 7 p. 1277- 1282
Objective - A transgenic mouse model was generated that allows conditional expression of human PLTP, based on the tetracycline-responsive gene system, to study the effects of an acute increase in plasma PLTP activity as may occur in inflammation. Methods and Results - The effects of an acute elevation of plasma PLTP activity on the metabolism of apolipoprotein B-containing lipoproteins and on diet-induced pre-existing atherosclerosis were determined in mice displaying a humanized lipoprotein profile (low-density lipoprotein receptor knockout background). Induced expression of PLTP strongly increases plasma VLDL levels in LDL receptor knockout mice, whereas VLDL secretion is not affected. The elevation in plasma triglyceride levels is explained by a PLTP-dependent inhibition of VLDL catabolism, which is caused, at least partly, by a decreased lipoprotein lipase activity. Together with the decreased plasma HDL levels, the acutely increased PLTP expression results in a highly atherogenic lipoprotein profile. Induction of PLTP expression leads to a further increase in size of pre-existing atherosclerotic lesions, even on a chow diet. In addition, the lesions contain more macrophages and less collagen relative to controls, suggesting a less stable lesion phenotype. Conclusion - In conclusion, acute elevation of PLTP activity destabilizes atherosclerotic lesions and aggravates pre-existing atherosclerosis.
|Lipoproteins, Phospholipid transfer protein, Transgenic mouse models, Triglycerides, atherosclerosis|
|Arteriosclerosis, Thrombosis, and Vascular Biology|
|Free full text at PubMed|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Moerland, M, Samyn, H.M.E, van Gent, T, van Haperen, M.J, Dallinga-Thie, G.M, Grosveld, F.G, … de Crom, M.P.G. (2008). Acute elevation of plasma PLTP activity strongly increases pre-existing atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology, 28(7), 1277–1282. doi:10.1161/ATVBAHA.108.165084