Hepatic Lipase Deficiency Increases Plasma Cholesterol but Reduces Susceptibility to Atherosclerosis in Apolipoprotein E-deficient Mice
| Autor: | Nobuyo Maeda, Robert Jones, Graciela Castro, Catherine Dengremont, Hafid Mezdour |
|---|---|
| Rok vydání: | 1997 |
| Předmět: |
Male
Apolipoprotein E medicine.medical_specialty Arteriosclerosis Lipoproteins Biology Biochemistry Mice Hepatic lipase deficiency Apolipoproteins E Plasma total cholesterol Plasma cholesterol Internal medicine medicine Deficient mouse Animals Molecular Biology Electrophoresis Agar Gel Arteries Lipase Cell Biology Lipids Mice Mutant Strains Cholesterol Endocrinology Liver Female lipids (amino acids peptides and proteins) Hepatic lipase Lipoproteins HDL |
| Zdroj: | Journal of Biological Chemistry. 272:13570-13575 |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.272.21.13570 |
| Popis: | The effect of hepatic lipase (HL) deficiency on the susceptibility to atherosclerosis was tested using mice with combined deficiencies in HL and apoE. Mice lacking both HL and apoE (hhee) have a plasma total cholesterol of 917 +/- 252 mg/dl (n = 24), which is 184% that of mice lacking only apoE (HHee; 497 +/- 161 mg/dl, n = 20, p0. 001). The increase in cholesterol was mainly in beta-migrating very low density lipoproteins, although high density lipoprotein cholesterol (HDLc) was also increased (53 +/- 37 versus 20 +/- 13 mg/dl, p0.01). Despite the increase in plasma cholesterol, we found that HL deficiency significantly decreased aortic plaque sizes in female mice fed normal chow (31 x 10(3) +/- 22 x 10(3) microm2 in hhee versus 115 x 10(3) +/- 69 x 10(3) microm2 in HHee, p0.001). Reduction of plaque sizes was also observed in female heterozygous apoE-deficient mice fed an atherogenic diet (2 x 10(3) +/- 2.5 x 10(3) microm2 in hhEe versus 56 x 10(3) +/- 49 x 10(3) microm2 in HHEe, p0.01). Changes in aortic lesion size were not apparent in the small number of male mice studied. In HHee females, both HDLc and the capacity of high density lipoprotein (HDL) particles to promote cholesterol efflux from cultured cells were 26% of the wild type. The absence of HL in hhee females partially restored HDLc levels to 57% and cholesterol efflux to 55% of the wild type. Circulating pre-beta1-migrating HDL were present in all mutants, suggesting that there are alternative pathways in the formation of these pre-beta-HDL not involving apoE, HL, or cholesteryl ester transfer protein. The improved capacity to promote cholesterol efflux, together with increased HDL, may explain why these animals can overcome the increase in atherogenic lipoproteins. |
| Databáze: | OpenAIRE |
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