Serum alpha_1-microglobulin variations in acute reaction phase
Serum alpha_1-microglobulin variations in acute reaction phase
批准号:
05671929
负责人:
KAWAI Tadashi
金额:
$1.15万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1994
中文摘要
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英文摘要
alpha1-microglobulin (alpha1-m) is a low molecular weight glycoportein of 30kDa synthesized at liver as most of proteins are. Serum variations of this protein were investigated both in patients with surgical operation and alpha-chain disease.2) alpha1-microglobulin clinically proved to be a positive acute phase reactant. Serum value was ellvated postoperatively depending on the synthetic capacity of the liver reserved. Since its molecular weight was low, it is easily cleared from kidney, that have so far made it impossible to define this protein as a acute phase reactant. Futrher fundamental study is under way to elucidate precise mechanisms of alpha1-m reaction at the liver.For clinical significance, total measurement of this protein can be useful as a sensitive indicator of liver function and its recovery.2) Structure analysis of an alpha-chain-alpha1-m complex in alpha-chain diseaseBasic structure of alpha-chain-alpha1-m complex is a heterodimer of Fcalpha and Fcalpha-alpha1-m complex, in latter of which alpha1-m covalently binds at 1 : 1 molar ratio. alpha1-m was extremely low in serum concentration as compared with that in alpha-chain.Immunohistochemical examinations have shown no alpha1-m positive localization in involved tissues, but structurally abnormal alpha-chain. A complex form should be synthesized elsewhere in the tissues in the body once alpha-chain is released into circulation from involved lymph nodes.3) Development of a serum amyloid A (SAA) assayIn the process of the present study, a precise assay for SAA was developed using a latex agglutination reaction.4) Mechanisms of alpha1-m synthesisEffects of Interleukin 6 was investigated on synthetic capacity of alpha1-m by a hepatoma cell line (cCH4) to show that the alpha1-m was reduced in its value in the supernatant fluids, which contradicted the clinical findings.
期刊论文(4)
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科研奖励(0)
会议论文
佐々木勝一他: "ラテックス凝集反応法を用いた血清アミロイドAの基礎的検討"
Katsuichi Sasaki 等人:“使用乳胶凝集法进行血清淀粉样蛋白 A 的基础研究”
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作者:
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通讯作者:
K.Sasaki, Y.Itoh, T.Kawai.: "A latex agglutination assay for serum amyloid A" IGAKU TO YAKUGAKU. (in press). (1995)
K.Sasaki、Y.Itoh、T.Kawai.:“血清淀粉样蛋白 A 的乳胶凝集测定” IGAKU TO YAKUGAKU。
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作者:
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通讯作者:
佐々木勝一: "ラテックス凝集反応法を用いた血清アミロイドAの基礎的検討" 薬学と医学. (in press). (1995)
Katsuichi Sasaki:“使用乳胶凝集法进行血清淀粉样蛋白 A 的基础研究”药理学和医学(1995 年出版)。
DOI:
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A study of bone regeneration by OCP/Collagen combined with MSC
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批准号:25870043
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项目类别:Grant-in-Aid for Young Scientists (B)
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资助金额:$2.75万
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财政年份:2013
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负责人:KAWAI Tadashi
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依托单位:
A clinical study of octacalcium phosphate collagen composite
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批准号:21800004
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项目类别:Grant-in-Aid for Research Activity Start-up
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资助金额:$1.7万
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财政年份:2009
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负责人:KAWAI Tadashi
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依托单位:
Synthesis of σ-π conjugated non-linear optical materials by olefin metathesis
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批准号:10650773
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.37万
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财政年份:1998
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负责人:KAWAI Tadashi
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依托单位:
Urine Protein profile System for Pathophysiologic Diagnosis of Renal and Urogenital Disorders
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批准号:07672496
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.6万
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财政年份:1995
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负责人:KAWAI Tadashi
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依托单位:
Purification of a new low molecular weight protein and its clinical application
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批准号:02454499
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项目类别:Grant-in-Aid for General Scientific Research (B)
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资助金额:$2.82万
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财政年份:1990
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负责人:KAWAI Tadashi
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依托单位:
国内基金
海外基金
Aquaporin介导的严重创伤后Interleukin-6致血脑屏障通透性增加的分子机制研究
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批准号:81801909
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项目类别:青年科学基金项目
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资助金额:22.0万元
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批准年份:2018
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负责人:杨思明
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依托单位:
Interleukin 6/gp130信号通路影响白癜风移植疗效的机制
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批准号:81271758
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项目类别:面上项目
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资助金额:70.0万元
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批准年份:2012
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负责人:许爱娥
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依托单位: