课题基金 / 基金详情

FUNCTION OF THE HEMOCHROMATOSIS PROTEIN

FUNCTION OF THE HEMOCHROMATOSIS PROTEIN
血色素沉着蛋白的功能
批准号:
6363024
负责人:
CAROLINE ENNS
金额:
$24.9万
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

项目摘要

项目成果

CAROLINE ENNS的其他基金

相似基金

相关文献

中文摘要
翻译
本应用的目的是确定与遗传性血色素沉着病有关的蛋白如何调节铁在上皮细胞屏障中的转运。遗传性血色素沉着症是一种铁超载导致特定器官铁积累的疾病。过量的铁会损害器官,导致各种各样的问题,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,大约每400人中就有1人患病。最近发现了这种疾病的基因,并发现其编码的蛋白(HFE)与主要的组织相容性I类蛋白相似。分子的序列对其功能的了解很少。初步结果和先前的数据表明,HFE是铁摄取的负调节因子,该基因的突变会导致功能丧失。一种模型认为,HFE通过感知铁转运蛋白(细胞基底外侧的转铁蛋白)的铁饱和度来调节铁跨越上皮细胞屏障的运输。铁通过转铁蛋白受体从基底外侧摄取,从而通过改变细胞内铁池来调节铁从细胞顶端到基底外侧的运输。该模型将通过测量表达HFE的细胞中转铁蛋白介导的和不依赖于转铁蛋白的铁摄取来进行测试,并与不表达HFE的细胞进行比较。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.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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
海外基金