Apolipoprotein E participates in the regulation of very low density lipoprotein-triglyceride secretion by the liver

被引:109
作者
Mensenkamp, AR
Jong, MC
van Goor, H
van Luyn, MJA
Bloks, V
Havinga, R
Voshol, PJ
Hofker, MH
van Dijk, KW
Havekes, LM
Kuipers, F
机构
[1] Univ Groningen Hosp, Ctr Liver Digest & Metab Dis, Groningen Inst Drug Studies, Dept Pediat, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen Hosp, Groningen Inst Drug Studies, Dept Pathol, NL-9713 GZ Groningen, Netherlands
[3] TNO Prevent & Hlth, Gaubius Lab, NL-2301 CE Leiden, Netherlands
[4] Leiden Univ, Ctr Med, Dept Human Genet, NL-2300 RA Leiden, Netherlands
[5] Leiden Univ, Ctr Med, Dept Cardiol, NL-2300 RA Leiden, Netherlands
[6] Leiden Univ, Ctr Med, Dept Internal Med, NL-2300 RA Leiden, Netherlands
[7] Univ Groningen, Fac Med Sci, Lab Cell Biol & Biomat, NL-9712 KZ Groningen, Netherlands
关键词
D O I
10.1074/jbc.274.50.35711
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ApoE-deficient mice on low fat diet show hepatic triglyceride accumulation and a reduced very low density lipoprotein (VLDL) triglyceride production rate. To establish the role of apoE in the regulation of hepatic VLDL production, the human APOE3 gene was introduced into apoE-deficient mice by cross-breeding with APOE3 transgenics (APOE3/apoe-/- mice) or by adenoviral transduction, APOE3 was expressed in the liver and, to a lesser extent, in brain, spleen, and lung of transgenic APOE3/apoe-/- mice similar to endogenous apoe, Plasma cholesterol levels in APOE/apoe-/- mice (3.4 +/- 0.5 mM) were reduced when compared with apoe-/- mice (12.6 +/- 1.4 mM) but still elevated when compared with wild type control values (1.9 +/- 0.1 mar). Hepatic triglyceride accumulation in apoE-deficient mice was completely reversed by introduction of the APOE3 transgene, The in vivo hepatic VLDL-triglyceride production rate was reduced to 36% of control values in apoE-deficient mice but normalized in APOE3/ apoe-/- mice. Hepatic secretion of apoB was not affected in either of the strains. Secretion of H-3-labeled triglycerides synthesized from [H-3]glycerol by cultured hepatocytes from apoE-deficient mice was four times lower than by APOE3/apoe-/- or control hepatocytes. The average size of secreted VLDL particles produced by cultured apoE-deficient hepatocytes was significantly reduced when compared with those of APOE3/ apoe-/- and wild type mice. Hepatic expression of human APOE3 cDNA via adenovirus-mediated gene transfer in apoE-deficient mice resulted in a reduction of plasma cholesterol depending on plasma apoE3 levels. The in vivo VLDL-triglyceride production rate in these mice was increased up to 500% compared with LacZ-injected controls and correlated with the amount of apoE3 per particle. These findings indicate a regulatory role of apoE in hepatic VLDL-triglyceride secretion, independent from its role in lipoprotein clearance.
引用
收藏
页码:35711 / 35718
页数:8
相关论文
共 43 条
[1]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[2]  
BOTTCHER CJF, 1961, ANAL CHIM ACTA, V24, P203
[3]  
CHOI SSY, 1994, J LIPID RES, V35, P848
[4]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[5]   THE ENHANCED ASSOCIATION OF APOLIPOPROTEIN-E WITH APOLIPOPROTEIN B-CONTAINING LIPOPROTEINS IN SERUM-STIMULATED HEPATOCYTES OCCURS INTRACELLULARLY [J].
FAZIO, S ;
YAO, ZM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (05) :593-600
[6]   VARIOUS RAT ADULT TISSUES EXPRESS ONLY ONE MAJOR MESSENGER-RNA SPECIES FROM THE GLYCERALDEHYDE-3-PHOSPHATE-DEHYDROGENASE MULTIGENIC FAMILY [J].
FORT, P ;
MARTY, L ;
PIECHACZYK, M ;
ELSABROUTY, S ;
DANI, C ;
JEANTEUR, P ;
BLANCHARD, JM .
NUCLEIC ACIDS RESEARCH, 1985, 13 (05) :1431-1442
[7]   DIFFERENT HYDROLYTIC EFFICIENCIES OF ADIPOSE-TISSUE LIPOPROTEIN-LIPASE ON VERY-LOW-DENSITY LIPOPROTEIN SUBFRACTIONS SEPARATED BY HEPARIN-SEPHAROSE CHROMATOGRAPHY [J].
GOMEZCORONADO, D ;
SAEZ, GT ;
LASUNCION, MA ;
HERRERA, E .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1167 (01) :70-78
[8]  
HAMILTON RL, 1991, J LIPID RES, V32, P529
[9]  
HAMILTON RL, 1990, J LIPID RES, V31, P1589
[10]   ADENOVIRUS-MEDIATED TRANSFER OF LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE ACUTELY ACCELERATES CHOLESTEROL CLEARANCE IN NORMAL MICE [J].
HERZ, J ;
GERARD, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2812-2816