Triglyceride-rich lipoproteins from apolipoprotein E3/2 subjects with hypertriglyceridemia enhance cholesteryl ester synthesis in human macrophages

被引:11
作者
Saito, M [1 ]
Eto, M [1 ]
Makino, I [1 ]
机构
[1] ASAHIKAWA MED COLL,DEPT INTERNAL MED 2,ASAHIKAWA,HOKKAIDO 078,JAPAN
关键词
apolipoprotein E; apolipoprotein E3/2; macrophage; hypertriglyceridemia; triglyceride-rich lipoproteins; cholesteryl ester synthesis;
D O I
10.1016/S0021-9150(96)06026-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ability of triglyceride (TG)-rich lipoproteins from apolipoprotein (ape) E2 heterozygote, apo E3/2 which is relatively common, to stimulate cholesteryl ester synthesis in human monocyte-derived macrophages was studied to clarify the atherogenicity of apo E3/2. Twenty-three subjects were randomly sampled from our hospitals, and divided into the following 4 groups: 7 apo E3/3 subjects with normolipidemia, 6 apo E3/3 subjects with hypertriglyceridemia (HTG), 5 apo E3/2 subjects with normolipidemia and 5 apo E3/2 subjects with HTG. Plasma levels of TG and total cholesterol (chol) were significantly (P < 0.001) higher in apo E3/3 and apo E3/2 subjects with HTG than in apo E3/3 and apo E3/2 subjects with normolipidemia, but plasma levels of TG and total chol were not significantly different between apo E3/3 and apo E3/2 subjects with HTG. [C-14]oleate incorporation into cholesteryl esters in macrophages was significantly (P < 0.001) higher in apo E3/2 subjects with HTG (0.661 nmol/mg cell protein) than in apo E3/3 subjects with normolipidemia (0.228) and with HTG (0.325) and in apo E3/2 subjects with normolipidemia (0.257). It is concluded that TG-rich lipoproteins from apolipoprotein E3/2 subjects with HTG enhance cholesteryl ester synthesis in human macrophages. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:73 / 77
页数:5
相关论文
共 28 条
  • [1] BASU SK, 1982, J BIOL CHEM, V257, P9788
  • [2] BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
  • [3] REVERSIBLE ACCUMULATION OF CHOLESTERYL ESTERS IN MACROPHAGES INCUBATED WITH ACETYLATED LIPOPROTEINS
    BROWN, MS
    GOLDSTEIN, JL
    KRIEGER, M
    HO, YK
    ANDERSON, RGW
    [J]. JOURNAL OF CELL BIOLOGY, 1979, 82 (03) : 597 - 613
  • [4] Brown MS, 1983, METABOLIC BASIS INHE, P655
  • [5] CUMMING AM, 1984, CLIN GENET, V25, P310
  • [6] APOLIPOPROTEIN-E POLYMORPHISM AND ATHEROSCLEROSIS
    DAVIGNON, J
    GREGG, RE
    SING, CF
    [J]. ARTERIOSCLEROSIS, 1988, 8 (01): : 1 - 21
  • [7] APOLIPOPROTEIN-E PHENOTYPING FROM PLASMA BY ISOELECTRIC-FOCUSING AND IMMUNOBLOTTING
    ETO, M
    WATANABE, K
    MORIYAMA, T
    MAKINO, I
    [J]. TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 160 (04) : 301 - 309
  • [8] ETO M, 1988, CLIN GENET, V34, P246
  • [9] ETO M, 1986, CLIN GENET, V30, P422
  • [10] A RAPID FLAT GEL ISOELECTRIC-FOCUSING METHOD FOR THE DETERMINATION OF APOLIPOPROTEIN-E PHENOTYPES AND ITS APPLICATION
    ETO, M
    WATANABE, K
    ISHII, K
    [J]. CLINICA CHIMICA ACTA, 1985, 149 (01) : 21 - 28