Adipomics ; Analysis of the physiological and pathological function of adipocyte
Adipomics ; Analysis of the physiological and pathological function of adipocyte
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
中文摘要
本研究的目的是阐明脂肪细胞和脂肪组织的功能,从临床上观察到许多生活方式相关疾病是由内脏脂肪的积累引发的,以及科学发现各种脂肪细胞衍生因子的异常是内脏肥胖相关疾病的共同基础,从而建立有效的策略来对抗糖尿病、动脉粥样硬化性血管疾病和某些与肥胖相关的LYFE相关疾病。从活体脂肪组织的三维分析来看,脂肪生成和血管生成的协调在肥胖脂肪组织的分化中起着至关重要的作用。脂肪组织中可见单核细胞卷曲和附着,类似于动脉粥样硬化早期的血管改变。被招募的巨噬细胞产生各种炎性细胞因子并影响脂肪细胞因子的产生,这被概念化为脂肪炎…。更多的苏改建。局部氧化应激和低氧的产生也被证明是脂肪细胞功能失调的可能机制。脂肪细胞的脂质体,即来自脂肪细胞的大泡结构,被解释为负责某种脂肪细胞因子分泌的机制。一些类型的体积感觉通道被认为是脂肪细胞增大的感受器,并部分地与肿瘤坏死因子α引起的葡萄糖摄取障碍有关。水通道蛋白7是水通道家族中的一个成员,是脂肪细胞中的一种甘油通道,其在体内的意义被证明为该分子的缺乏会导致严重的饥饿低血糖。研究表明,脂肪细胞来源的防御分子脂联素的意义,以及脂联素缺乏,低脂联素血症(通常和临床上观察到的内脏脂肪堆积)在代谢综合征的疾病发展中起着重要作用。脂联素可能的受体AdipoR1和R2的鉴定以及对缺乏这些分子的小鼠的精确分析证实了脂联素在活体中的重要性。我们相信,本项目所进行的研究确实为建立一个新的研究领域--脂肪组学--做出了贡献,这是对抗LYFE相关疾病,特别是爆炸性流行的心血管疾病所必需的
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
メタボリックシンドローム:その臨床的意義と発症のメカニズム
代谢综合征:其临床意义和发病机制
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:
Mae T, et al.: "A licorice ethanolic extract with PPAR-γ ligand-binding activity affects diabetes in KK-Ay mice, abdominal obesity in diet-Induced obese C57BL mice and Hypertension in spontaneously hypertensive rats."J.Nutrition. 133. 3369-3377 (2003)
Mae T 等人:“具有 PPAR-γ 配体结合活性的甘草乙醇提取物可影响 KK-Ay 小鼠的糖尿病、饮食诱导的肥胖 C57BL 小鼠的腹部肥胖以及自发性高血压大鼠的高血压。”J.Nutrition 133。 .3369-3377 (2003)
DOI:
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发表时间:
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共 645 条
Discovery of adipose specific glycerol channel and its application to obesity therapy
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批准号:12557090
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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
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批准号:12307022
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项目类别:Grant-in-Aid for Scientific Research (A)
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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
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批准号:10044281
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项目类别:Grant-in-Aid for Scientific Research (B).
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资助金额:$3.65万
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财政年份:1998
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负责人:MATSUZAWA Yuji
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依托单位:
Identification of adipose-specific genes and teir clinical significance
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批准号:10557101
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.0万
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财政年份:1998
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负责人:MATSUZAWA Yuji
-
依托单位:
Molecular pathogenesis and mechanism of vidseral obesity
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批准号:09307019
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$24.45万
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财政年份:1997
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负责人:MATSUZAWA Yuji
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依托单位:
Development of Gene Therapy for Familial Hypercholesterolemia-in vivo gene transfer to hepatocytes by HVJ-liposome-retrovirus method-
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批准号:08557062
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$9.73万
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财政年份:1996
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负责人:MATSUZAWA Yuji
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依托单位:
International Study on Gene Abnormalities of GETP and LDL-Receptor
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批准号:08044280
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$4.03万
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财政年份:1996
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负责人:MATSUZAWA Yuji
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依托单位:
Development of Therapy for Refractory Hyperlipidemia with LDL Receptor Gene Introduction by Lipofection Method
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批准号:06557059
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项目类别:Grant-in-Aid for Developmental Scientific Research (B)
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资助金额:$7.23万
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财政年份:1994
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负责人:MATSUZAWA Yuji
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依托单位:
Cell-biological and molecular biological analyzes of reverse cholesterol transport as a protective system against atherosclerosis
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批准号:04404085
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项目类别:Grant-in-Aid for General Scientific Research (A)
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资助金额:$20.16万
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财政年份:1992
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负责人:MATSUZAWA Yuji
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依托单位:
Studies on the Preventive System Against Atherosclerosis Based on the Discovery of Cases With Choles-Terol Ester Transfer Protein Deficiency.
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批准号:01480289
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项目类别:Grant-in-Aid for General Scientific Research (B)
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资助金额:$4.29万
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财政年份:1989
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负责人:MATSUZAWA Yuji
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依托单位:
Studies on Pathogenesis and Pathophysiology of Visceral Fat Obesity, a New Criteria of Obesity based on fat Topography
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批准号:62480255
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项目类别:Grant-in-Aid for General Scientific Research (B)
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资助金额:$3.71万
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财政年份:1987
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负责人:MATSUZAWA Yuji
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依托单位:
海外基金