Adipomics ; Analysis of the physiological and pathological function of adipocyte
脂肪组学;
基本信息
- 批准号:15081101
- 负责人:
- 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
- 起止时间:2003 至 2007
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
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
该研究领域的目的是阐明脂肪细胞和脂肪组织的功能,以建立一种有效的策略来对抗与Lyfe型相关的疾病,如糖尿病,动脉粥样硬化性血管疾病和某些类型的癌症与肥胖有关,从临床观察,许多生活方式相关的疾病是由内脏脂肪的积累和科学发现,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症中脂肪组织的分化中起着重要作用。在脂肪组织中观察到单核细胞的滚动和附着,类似于早期动脉粥样硬化血管变化。募集的巨噬细胞产生各种炎症细胞因子,并影响脂肪细胞因子的产生,这被认为是脂肪组织的一个概念。 ...更多信息 苏重塑。局部氧化应激和缺氧也被证明是脂肪细胞因子失调的潜在机制。脂肪体,脂肪细胞的大泡状结构被阐明为负责某种脂肪细胞因子分泌的机制。某些类型的体积感应通道被确定为脂肪细胞增大的传感器,并部分负责TNF α诱导的葡萄糖摄取障碍。水通道蛋白7(Aquaporin 7)是水通道家族的成员之一,是脂肪细胞中的甘油通道,其在机体中的重要性已被证明,缺乏该分子可导致饥饿时严重的低血糖;脂联素(Adiponectin)是脂肪细胞的防御性分子,大量研究揭示了脂联素缺乏、低脂联素血症、(这通常和临床上在内脏脂肪积聚中观察到)在代谢综合征中的病症的发展中起重要作用。AdipoR 1和R2是脂联素的可能受体,AdipoR 1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体内的重要性。我们相信,在本项目中进行的研究确实为一个名为“肥胖症”的新研究领域的基础性建立做出了贡献,该研究领域必须与Lyfe型相关疾病,特别是世界上爆炸性流行的心血管疾病作斗争。
项目成果
期刊论文数量(1399)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Role of Kruppel-like factor 15 in PEPCK gene expression in the liver
- DOI:10.1016/j.bbrc.2004.12.096
- 发表时间:2005-02-18
- 期刊:
- 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:0
- 作者:Keiichiro Susuki;et. al.;Maekawa F;小川 渉
- 通讯作者:小川 渉
SREBP1 is required for the induction by glucose of pancreatic beta-cell genes involved in glucose sensing.
- DOI:10.1194/jlr.m700533-jlr200
- 发表时间:2008-04
- 期刊:
- 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:0
- 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:
- 发表时间:
- 期刊:
- 影响因子:0
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MATSUZAWA Yuji其他文献
MATSUZAWA Yuji的其他文献
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{{ truncateString('MATSUZAWA Yuji', 18)}}的其他基金
Discovery of adipose specific glycerol channel and its application to obesity therapy
脂肪特异性甘油通道的发现及其在肥胖治疗中的应用
- 批准号:
12557090 - 财政年份:2000
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
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
新型脂肪细胞衍生因子的发现及其在人类中的病理和生理作用;
- 批准号:
12307022 - 财政年份:2000
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Molecular mechanism of visceral fat syndrome, common basis of atherosclerotic diseases
内脏脂肪综合征的分子机制,动脉粥样硬化疾病的共同基础
- 批准号:
10044281 - 财政年份:1998
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (B).
Identification of adipose-specific genes and teir clinical significance
脂肪特异性基因的鉴定及其临床意义
- 批准号:
10557101 - 财政年份:1998
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular pathogenesis and mechanism of vidseral obesity
内脏肥胖的分子发病机制及机制
- 批准号:
09307019 - 财政年份:1997
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Development of Gene Therapy for Familial Hypercholesterolemia-in vivo gene transfer to hepatocytes by HVJ-liposome-retrovirus method-
家族性高胆固醇血症基因疗法的开发-通过HVJ-脂质体-逆转录病毒方法将基因体内转移至肝细胞-
- 批准号:
08557062 - 财政年份:1996
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
International Study on Gene Abnormalities of GETP and LDL-Receptor
GETP 和 LDL 受体基因异常的国际研究
- 批准号:
08044280 - 财政年份:1996
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for international Scientific Research
Development of Therapy for Refractory Hyperlipidemia with LDL Receptor Gene Introduction by Lipofection Method
脂质转染法导入LDL受体基因治疗难治性高脂血症的进展
- 批准号:
06557059 - 财政年份:1994
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
Cell-biological and molecular biological analyzes of reverse cholesterol transport as a protective system against atherosclerosis
反向胆固醇转运作为动脉粥样硬化保护系统的细胞生物学和分子生物学分析
- 批准号:
04404085 - 财政年份:1992
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for General Scientific Research (A)
Studies on the Preventive System Against Atherosclerosis Based on the Discovery of Cases With Choles-Terol Ester Transfer Protein Deficiency.
基于发现胆固醇-三醇酯转移蛋白缺陷病例的动脉粥样硬化预防系统研究。
- 批准号:
01480289 - 财政年份:1989
- 资助金额:
$ 26.82万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
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Mechanisms of adipocytokine control of cardiovascular diseases through the regulation of multi organ network
脂肪细胞因子通过调节多器官网络控制心血管疾病的机制
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26893335 - 财政年份:2014
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