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FUNCTION OF THE HEMOCHROMATOSIS PROTEIN

FUNCTION OF THE HEMOCHROMATOSIS PROTEIN
血色素沉着蛋白的功能
批准号:
6043444
负责人:
CAROLINE ENNS
金额:
$24.33万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-03-01 至 2004-02-29

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中文摘要
翻译
本申请的目的是确定与遗传性血色病有关的蛋白质如何发挥作用以调节铁转运穿过上皮细胞屏障。遗传性血色病是一种铁超负荷导致铁在特定器官中积累的疾病。 过量的铁会损害器官并导致各种问题,如肝功能衰竭、成人糖尿病、心力衰竭、关节炎和肝癌。 它是欧洲人后裔中最常见的遗传性疾病,影响约400人中的1人。 最近,这种疾病的基因被确定,它编码的蛋白质(HFE)被发现是类似的主要组织相容性I类蛋白。 分子的序列使我们对它的功能知之甚少。 初步结果和以前的数据表明,HFE是铁吸收的负调节因子,基因突变会导致功能丧失。 一种模型是HFE通过检测铁转运蛋白(细胞基底侧的转铁蛋白)的铁饱和度来调节铁转运穿过上皮细胞屏障。 通过转铁蛋白受体从基底侧摄取铁,然后通过改变细胞内铁池来调节从细胞顶端到基底侧的铁转运。 将通过测量表达HFE的细胞中转铁蛋白介导的和转铁蛋白非依赖性的铁摄取并与不表达HFE的细胞进行比较来测试该模型。 这些研究的长期目标是确定铁在体内的运输是如何调节的。
英文摘要
The goal of the present application is to determine how the protein implicated in hereditary hemochromatosis functions to regulate iron transport across epithelial cell barriers. Hereditary hemochromatosis is a disease of iron overload leading to iron accumulation in specific organs over the life time of the individual. Excess iron damages organs and results in a variety of problems such as liver failure, adult onset diabetes, heart failure, arthritus and hepatoma. It is the most common inherited disease in people of European descent affecting approximately 1 in 400 individuals. Recently the gene for this disease was identified and the protein it encodes (HFE) found to be similar to major histocompatibility class I proteins. The sequence of the molecule gives little insight into its function. Data obtained for preliminary results and previous data suggest that HFE is a negative regulator of iron uptake and mutations in the gene cause a loss of function. One model would be that HFE regulates iron transport across epithelial cell barriers by sensing the iron saturation of the iron transport protein, transferrin on the basolateral side of the cell. Iron uptake from the basolateral side via the transferrin receptor then would regulate iron transport from the apical to the basolateral side of the cell by altering intracellular iron pools. The model will be tested by measuring transferrin-meditated and transferrin- independent iron uptake in cells expressing HFE and compared to cells not expressing HFE. The long term goal of these studies is to determine how the transport of iron is regulated in the body.
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Regulation of hepatic hepcidin expression by transferrin receptor-2
Regulation of hepatic hepcidin expression by transferrin receptor-2
Regulation of hepatic hepcidin expression by transferrin receptor-2
FUNCTION OF THE HEMOCHROMATOSIS PROTEIN
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