Identification of novel transporter for exporting iron to establish effective therapy for chronic liver disorder
Identification of novel transporter for exporting iron to establish effective therapy for chronic liver disorder
批准号:
24659358
负责人:
MIZOKAMI Yuji
金额:
$2.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2012
资助国家:
日本
项目状态:
已结题
起止时间:
2012-04-01 至 2014-03-31
中文摘要
由于体内过量的铁积累引起氧化应激,需要有效的铁排泄系统。令人惊讶的是,在这个系统中只发现了一种名为FPN1的分子。在这项研究中,我们旨在通过关注在抗氧化应激基因诱导中起核心作用的Nrf2调控表达的基因来鉴定新的铁输出蛋白。通过微阵列分析,列出了SLC40A1、HFE、FECH、CYBRD1、ISCU、SLC25A37和TFRC等候选蛋白,但它们都不具有铁出口活性。
英文摘要
As excess iron accumulation in body cause oxidative stress, it is needed that effective iron excretion system. Surprisingly, there is only one molecule named FPN1 has been identified in this system. In this study, we aimed to identify novel iron exporting protein by focusing on the genes that expressions are regulated by Nrf2 having central role for anti-oxidative stress gene induction. By using microarray analysis, some candidates such as SLC40A1, HFE, FECH, CYBRD1, ISCU, SLC25A37 and TFRC were listed up, however, all of those did not have iron exporting activity.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
Obesity in p62-KO mice is prevented by estradiol
雌二醇可预防 p62-KO 小鼠的肥胖
DOI:
--
发表时间:
2014
期刊:
影响因子:
--
作者:
[Eiji Warabi, Kentaro Akiyama, Junichi Shoda, Tetsuro Ishii]
通讯作者:
Tetsuro Ishii
p62/Sqstm1欠損は中枢におけるレプチン抵抗性により過食を引き起こす
p62/Sqstm1 缺乏会因中枢瘦素抵抗而导致食欲亢进
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[蕨栄治, 石井哲郎, 正田純一.]
通讯作者:
正田純一.
The regulatory role of fatty acid metabolism in development of NASH
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批准号:16K15188
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
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财政年份:2016
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负责人:MIZOKAMI Yuji
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依托单位:
海外基金