Angptl3 regulates lipid metabolism in mice

被引:0
|
作者
Ryuta Koishi
Yosuke Ando
Mitsuru Ono
Mitsuru Shimamura
Hiroaki Yasumo
Toshihiko Fujiwara
Hiroyoshi Horikoshi
Hidehiko Furukawa
机构
[1] Biomedical Research Laboratories,
[2] Sankyo Co.,undefined
[3] Ltd.,undefined
[4] Medicinal Safety Research Laboratories,undefined
[5] Sankyo Co.,undefined
[6] Ltd.,undefined
[7] Pharmacology & Molecular Biology Research Laboratories,undefined
[8] Sankyo Co.,undefined
[9] Ltd.,undefined
[10] Sankyo Pharma Research Institute,undefined
来源
Nature Genetics | 2002年 / 30卷
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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 (hypl) 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 Angptl3 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.
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页码:151 / 157
页数:6
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