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Molecular Mechanism of Vitamine E recycling in vivo.

Molecular Mechanism of Vitamine E recycling in vivo.
维生素 E 体内回收的分子机制。
批准号:
07672346
负责人:
ARAI Hiroyuki
金额:
$1.6万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996

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中文摘要
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英文摘要
Alpha-tocopherol, the most biologcally active form of vitamin E,is a lipid soluble antioxidant that protects membranes from oxidative stresses. Vitamin E occurs in nature in eight different forms, but animal body is enriched in alpha-tocopherol compared with other forms. Studies on the transport vitamin E in animals and man suggest that the liver plays a key role in the preferential retention, and subsequent distribution of alpha-tocopherol to tissues, but little was known about the mechanism. Alpha-tocopherol transfer protein (alpha-TTP) is a cytosolic liver protein with highly specific binding ability for alpha-tocopherol. Alpha-TTP also has an ability to transport alpha-tocopherol between membranes in vitro. We have succeeded in purifying this protein from rat liver and isolating its cDNA from rat and human. Furthermore, we have demonstrated that the mutations in the gene that encodes alpha-TTP cause ataxia with familial vitamin E deficiecy. Patients with this disease have low or undetectable serum alpha-tocopherol concentrations and progressive spinocerebellar dysfunction. In these patients, the absorption of alpha-tocopherol from intestine and the transport to the liver is normal, but they have an impaired ability to incorporate alpha-tocopherol into VLDL in the liver. From these observation, it was found that alpha-TTP catalyze the transfer of alpha-tocopherol taken up by the liver into nascent VLDL.
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会议论文
Takanari Gotoda: "Adult-onset spinocerebellar dysfunction caused by a mutation in the gene for the alpha-tocopherol-transfer protein" The New Eng. J.of Med.333. 1313-1318 (1995)
Takanari Gotoda:“由α-生育酚转移蛋白基因突变引起的成人脊髓小脑功能障碍”《新英格兰》。
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通讯作者:
Karim Ouahchi: "Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein" Nature Genet.9. 141-145 (1995)
Karim Ouahchi:“伴有孤立性维生素 E 缺乏的共济失调是由 α-生育酚转移蛋白突变引起的”Nature Genet.9。
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新井洋由: "ビタミンE輸送タンパク質と先天性ビタミンE欠乏症" 日本油化学会誌, 10 (1996)
新井博吉:“维生素E转运蛋白和先天性维生素E缺乏症”日本油脂化学会杂志,10(1996)
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通讯作者:
Yokota T.et al.: "Retinitis Pigmentosa and Ataxia Caused by a Mutation in the Gene for the α-Tocopherol Transfer Protein" N.Engl.J.Med.335. 1770-1771 (1996)
Yokota T.等人:“α-生育酚转移蛋白基因突变引起的视网膜色素变性和共济失调”N.Engl.J.Med.335(1996)。
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