TRANSGENIC MICE EXPRESSING HIGH PLASMA-CONCENTRATIONS OF HUMAN APOLIPOPROTEIN B100 AND LIPOPROTEIN(A)

被引:203
作者
LINTON, MF
FARESE, RV
CHIESA, G
GRASS, DS
CHIN, P
HAMMER, RE
HOBBS, HH
YOUNG, SG
机构
[1] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,SAN FRANCISCO,CA 94141
[2] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94141
[3] DNX BIOTHERAPEUT INC,PRINCETON,NJ 08540
[4] UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET & INTERNAL MED,DALLAS,TX 75235
[5] UNIV TEXAS,SW MED CTR,DEPT BIOCHEM,DALLAS,TX 75235
[6] UNIV TEXAS,SW MED CTR,HOWARD HUGHES MED INST,DALLAS,TX 75235
[7] UNIV CALIF SAN FRANCISCO,GLADSTONE INST CARDIOVASC DIS,POB 4191000,SAN FRANCISCO,CA 94141
关键词
P1; BACTERIOPHAGE; LOW DENSITY LIPOPROTEINS; CHOLESTEROL;
D O I
10.1172/JCI116927
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The B apolipoproteins, apo-B48 and apo-B100, are key structural proteins in those classes of lipoproteins considered to be atherogenic [e.g., chylomicron remnants, beta-VLDL, LDL, oxidized LDL, and Lp(a)]. Here we describe the development of transgenic mice expressing high levels of human apo-B48 and apo-B100. A 79.5-kb human genomic DNA fragment containing the entire human apo-B gene was isolated from a PI bacteriophage library and microinjected into fertilized mouse eggs. 16 transgenic founders expressing human apo-B were generated, and the animals with the highest expression had plasma apo-B100 levels nearly as high as those of normolipidemic humans (approximately 50 mg/dl). The human apo-B100 in transgenic mouse plasma was present largely in lipoproteins of the LDL class as shown by agarose gel electrophoresis, chromatography on a Superose 6 column, and density gradient ultracentrifugation. When the human apo-B transgenic founders were crossed with transgenic mice expressing human apo(a), the offspring that expressed both transgenes had high plasma levels of human Lp(a). Both the human apo-B and Lp(a) transgenic mice will be valuable resources for studying apo-B metabolism and the role of apo-B and Lp(a) in atherosclerosis.
引用
收藏
页码:3029 / 3037
页数:9
相关论文
共 51 条
  • [1] BLACKHART BD, 1986, J BIOL CHEM, V261, P5364
  • [2] A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS
    BROWN, MS
    GOLDSTEIN, JL
    [J]. SCIENCE, 1986, 232 (4746) : 34 - 47
  • [3] APOLIPOPROTEIN B-48 IS THE PRODUCT OF A MESSENGER-RNA WITH AN ORGAN-SPECIFIC IN-FRAME STOP CODON
    CHEN, SH
    HABIB, G
    YANG, CY
    GU, ZW
    LEE, BR
    WENG, SA
    SILBERMAN, SR
    CAI, SJ
    DESLYPERE, JP
    ROSSENEU, M
    GOTTO, AM
    LI, WH
    CHAN, L
    [J]. SCIENCE, 1987, 238 (4825) : 363 - 366
  • [4] CHIESA G, 1992, J BIOL CHEM, V267, P24369
  • [5] A STUDY OF ATHEROSCLEROSIS REGRESSION IN MACACA-MULATTA .5. CHANGES IN ABDOMINAL-AORTA AND CAROTID AND CORONARY-ARTERIES FROM ANIMALS WITH ATHEROSCLEROSIS INDUCED FOR 38 MONTHS AND THEN REGRESSED FOR 24 OR 48 MONTHS AT PLASMA-CHOLESTEROL CONCENTRATIONS OF 300 OR 200 MG/DL
    CLARKSON, TB
    BOND, MG
    BULLOCK, BC
    MCLAUGHLIN, KJ
    SAWYER, JK
    [J]. EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1984, 41 (01) : 96 - 118
  • [6] DETERMINATION OF CYSTEINE ON LOW-DENSITY LIPOPROTEINS USING THE FLUORESCENT-PROBE, 5-IODOACETAMIDOFLUORESCEINE
    COLEMAN, RD
    KIM, TW
    GOTTO, AM
    YANG, CY
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1037 (01) : 129 - 132
  • [7] ABILITY OF THE LDL RECEPTOR FROM SEVERAL ANIMAL SPECIES TO RECOGNIZE THE HUMAN APO-B BINDING DOMAIN - STUDIES WITH LDL FROM FAMILIAL DEFECTIVE APO-B-100
    CORSINI, A
    MAZZOTTI, M
    VILLA, A
    MAGGI, FM
    BERNINI, F
    ROMANO, L
    ROMANO, C
    FUMAGALLI, R
    CATAPANO, AL
    [J]. ATHEROSCLEROSIS, 1992, 93 (1-2) : 95 - 103
  • [8] CURTISS LK, 1982, J BIOL CHEM, V257, P5213
  • [9] DIXON JL, 1993, J LIPID RES, V34, P167
  • [10] FARESE RV, 1992, J LIPID RES, V33, P569