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Adipomics ; Analysis of the physiological and pathological function of adipocyte

Adipomics ; Analysis of the physiological and pathological function of adipocyte
脂肪组学;
批准号:
15081101
负责人:
MATSUZAWA Yuji
金额:
$26.82万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2007

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中文摘要
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英文摘要
The aim of this research field is to clarify the functions of adipocyte and adipose tissue to establish an effective strategy for combating lyfe-style-related disorders such as diabetes, atherosclerotic vascular diseases and some types of cancers related to obesity from the clinical observations that many life-style-related disorders are triggered by the accumulation of visceral fat and scientific findings that abnormalities of various adipocyte-derived factors conceptualized as adipocytokines reside a common basis of visceral obesity-related disorders.From three-dimensional analyses of living adipose tissue, coordination of adipogenesis and angiogenesis plays an essential role in the differentiation of adipose tissue in obesity. Rolling and attachment of monocytes were observed in adipose tissue resembling early atherosclerotic vascular changes. Recruited macrophages produced various inflammatory cytokines and affected adipocytokines production, which was conceptualized as adipose tis … More sue remodeling. Local production of oxidative stress and hypoxia also were also proved as underlying possible mechanisms of adipocutokine dysregulation.Adiposome, macrovesicular structure from adipocyte was elucidated as machinery responsible for some kind of adipocytokine secretion. Some types of volume sensing channel were identified as a sensor of adipocyte enlargement and partially responsible for TNF α-induced impairment of glucose uptake. Aquaporin 7, a member of water channel family, was identified as a glycerol channel in adipocyte, and its significance in the body was proved by the fact that the deficiency of this molecule caused profound hypoglycemia in starvation.Vast researches revealed the significance of adiponectin, a defensive molecule derived from adipocyte, and deficiency of adiponectin, hypoadiponectinemia, (which is usually and clinically observed in visceral fat accumulation) plays important roles in the development of disorders in the metabolic syndrome. Idntifycation of AdipoRl and R2, which are possible receptors for adiponectin and precise analyses of mice lacking these molecules confirmed the importance of adiponectin in vivo.We believe that the researches performed in this project really contributed fundamental establishment of a new research field named 'adipomics', which must be required to fight against lyfe-style-related disorders, especially cardiovascular disease explosively prevailing the world Less
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DOI: 10.1016/j.bbrc.2004.12.096
发表时间: 2005-02-18
期刊: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
影响因子: 3.1
作者: [Teshigawara, K, Ogawa, W, Kasuga, M]
通讯作者: Kasuga, M
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [Keiichiro Susuki, et. al., Maekawa F, 小川 渉]
通讯作者: 小川 渉
DOI: 10.1194/jlr.m700533-jlr200
发表时间: 2008-04
期刊: Journal of lipid research
影响因子: 6.5
作者: [Diraison F, Ravier MA, Richards SK, Smith RM, Shimano H, Rutter GA]
通讯作者: Rutter GA
Kamei Y, et al.: "A forkhead transcription factor FKHR up-regulates lipoprotein lipase expression in skeletal muscle"FEBS Lett.. 536. 232-236 (2003)
Kamei Y 等人:“叉头转录因子 FKHR 上调骨骼肌中的脂蛋白脂肪酶表达”FEBS Lett.. 536. 232-236 (2003)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
645
    Discovery of adipose specific glycerol channel and its application to obesity therapy
    • 批准号:
      12557090
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $7.81万
    • 财政年份:
      2000
    • 负责人:
      MATSUZAWA Yuji
    • 依托单位:
    Discovery of Novel Adipocyte-Derived Factors and Their Pathological and Physiological Roles in Humans; Adipocentric Hypothesis in Molecular Basis for the Development of Common Diseases
    • 批准号:
      12307022
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $25.72万
    • 财政年份:
      2000
    • 负责人:
      MATSUZAWA Yuji
    • 依托单位:
    Molecular mechanism of visceral fat syndrome, common basis of atherosclerotic diseases
    • 批准号:
      10044281
    • 项目类别:
      Grant-in-Aid for Scientific Research (B).
    • 资助金额:
      $3.65万
    • 财政年份:
      1998
    • 负责人:
      MATSUZAWA Yuji
    • 依托单位:
    Identification of adipose-specific genes and teir clinical significance
    • 批准号:
      10557101
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $8.0万
    • 财政年份:
      1998
    • 负责人:
      MATSUZAWA Yuji
    • 依托单位:
    海外基金