Angptl3 regulates lipid metabolism in mice

被引:347
作者
Koishi, R
Ando, Y
Ono, M
Shimamura, M
Yasumo, H
Fujiwara, T
Horikoshi, H
Furukawa, H
机构
[1] Sankyo Co Ltd, Biomed Res Labs, Shinagawa Ku, Tokyo 1408710, Japan
[2] Sankyo Co Ltd, Med Safety Res Labs, Shizuoka 4370065, Japan
[3] Sankyo Co Ltd, Pharmacol & Mol Biol Res Labs, Shinagawa Ku, Tokyo 1408710, Japan
[4] Sankyo Pharma Res Inst, La Jolla, CA 92037 USA
关键词
D O I
10.1038/ng814
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The KK obese mouse is moderately obese and has abnormally high levels of plasma insulin (hyperinsulinemia), glucose (hyperglycemia) and lipids (hyperlipidemia). In one strain (KK/San), we observed abnormally low plasma lipid levels (hypolipidemia). This mutant phenotype is inherited recessively as a mendelian trait. Here we report the mapping of the hypolipidemia (hypo locus to the middle of chromosome 4 and positional cloning of the autosomal recessive mutation responsible for the hypolipidemia. The hypl locus encodes a unique angiopoietin-like lipoprotein modulator, which we named Allm1. it is identical to angiopoietin-like protein 3, encoded by Angptl3, and has a highly conserved counterpart in humans. Overexpression of Angpl3 or intravenous injection of the purified protein in KK/San mice elicited an increase in circulating plasma lipid levels. This increase was also observed in C57BL/6J normal mice. Taken together, these data suggest that Angptl3 regulates lipid metabolism in animals.
引用
收藏
页码:151 / 157
页数:7
相关论文
共 38 条
  • [1] The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
    Bodzioch, M
    Orsó, E
    Klucken, T
    Langmann, T
    Böttcher, L
    Diederich, W
    Drobnik, W
    Barlage, S
    Büchler, C
    Porsch-Özcürümez, M
    Kaminski, WE
    Hahmann, HW
    Oette, K
    Rothe, G
    Aslanidis, C
    Lackner, KJ
    Schmitz, G
    [J]. NATURE GENETICS, 1999, 22 (04) : 347 - 351
  • [2] Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
    Brooks-Wilson, A
    Marcil, M
    Clee, SM
    Zhang, LH
    Roomp, K
    van Dam, M
    Yu, L
    Brewer, C
    Collins, JA
    Molhuizen, HOF
    Loubser, O
    Ouelette, BFF
    Fichter, K
    Ashbourne-Excoffon, KJD
    Sensen, CW
    Scherer, S
    Mott, S
    Denis, M
    Martindale, D
    Frohlich, J
    Morgan, K
    Koop, B
    Pimstone, S
    Kastelein, JJP
    Genest, J
    Hayden, MR
    [J]. NATURE GENETICS, 1999, 22 (04) : 336 - 345
  • [3] MYOCARDIAL-INFARCTION IN FAMILIAL FORMS OF HYPERTRIGLYCERIDEMIA
    BRUNZELL, JD
    SCHROTT, HG
    MOTULSKY, AG
    BIERMAN, EL
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1976, 25 (03): : 313 - 320
  • [4] Identification of a mammalian angiopoietin-related protein expressed specifically in liver
    Conklin, D
    Gilbertson, D
    Taft, DW
    Maurer, MF
    Whitmore, TE
    Smith, DL
    Walker, KM
    Chen, LH
    Wattler, S
    Nehls, M
    Lewis, KB
    [J]. GENOMICS, 1999, 62 (03) : 477 - 482
  • [5] Isolation of Angiopoietin-1, a ligand for the TIE2 receptor, by secretion-trap expression cloning
    Davis, S
    Aldrich, TH
    Jones, PF
    Acheson, A
    Compton, DL
    Jain, V
    Ryan, TE
    Bruno, J
    Radziejewski, C
    Maisonpierre, PC
    Yancopoulos, GD
    [J]. CELL, 1996, 87 (07) : 1161 - 1169
  • [6] APOLIPOPROTEIN-B GENE-MUTATIONS AFFECTING CHOLESTEROL LEVELS
    FARESE, RV
    LINTON, MF
    YOUNG, SG
    [J]. JOURNAL OF INTERNAL MEDICINE, 1992, 231 (06) : 643 - 652
  • [7] Identification and chromosomal assignment of USP1, a novel gene encoding a human ubiquitin-specific protease
    Fujiwara, T
    Saito, A
    Suzuki, M
    Shinomiya, H
    Suzuki, T
    Takahashi, E
    Tanigami, A
    Ichiyama, A
    Chung, CH
    Nakamura, Y
    Tanaka, K
    [J]. GENOMICS, 1998, 54 (01) : 155 - 158
  • [8] FAMILIAL LIPOPROTEIN DISORDERS IN PATIENTS WITH PREMATURE CORONARY-ARTERY DISEASE
    GENEST, JJ
    MARTINMUNLEY, SS
    MCNAMARA, JR
    ORDOVAS, JM
    JENNER, J
    MYERS, RH
    SILBERMAN, SR
    WILSON, PWF
    SALEM, DN
    SCHAEFER, EJ
    [J]. CIRCULATION, 1992, 85 (06) : 2025 - 2033
  • [9] HYPERLIPIDEMIA IN CORONARY HEART-DISEASE .2. GENETIC ANALYSIS OF LIPID-LEVELS IN 176 FAMILIES AND DELINEATION OF A NEW INHERITED DISORDER, COMBINED HYPERLIPIDEMIA
    GOLDSTEIN, JL
    SCHROTT, HG
    HAZZARD, WR
    BIRMAN, EL
    MOTULSKY, AG
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (07) : 1544 - 1568
  • [10] GREENFIELD M, 1980, DIABETOLOGIA, V18, P441