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Oxidized Phospholipids in Vascular Pathobiology

Oxidized Phospholipids in Vascular Pathobiology
血管病理学中的氧化磷脂
批准号:
8101061
负责人:
Thomas M McIntyre
金额:
$228.08万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-06 至 2013-04-30

项目摘要

项目成果

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this Program is to develop a mechanistic understanding of the link between lipid oxidation and vascular pathology. The senior research team is a highly interactive multidisciplinary group with a broad range of shared expertise, including cell biology, chemical biology, biochemistry, and immunology. The 4 interrelated projects will test the hypothesis that oxidation of phospholipids in lipoproteins and cell membranes creates specific ligands for vascular cell receptors, transporters, and enzymes that then drastically alter cellular function and contribute to the pathogenesis of inflammatory diseases, including atherosclerosis. Project 1 will combine biophysical and clinical studies to define the chemical structures, biophysical properties, and oxidative pathways that participate in the formation, decay, and receptor binding activities of a novel family of specific oxidized phospholipid ligands of the Class B scavenger receptor CD36. This project will also assess the clinical relevance of specific oxidized phospholipids in human athero-sclerosis. Project 2 will determine how vascular cells clear biologically active and toxic components of oxLDL by defining the fate of extracellular oxidized phospholipids, characterizing transporters and transport mechanisms of oxidized phospholipids, and determining signaling pathways connecting oxLDL and phospholipids to cell viability. Project 3 will define complex mechanisms that regulate expression and activity of monocyte/macrophage 15- lipoxygenase, the enzyme responsible for producing 13-HPODE, an oxidation product of linoleic acid and a prominent oxidized lipid found in atheroma. Project 4 will define vascular cell signaling pathways initiated by binding of specific oxidized phospholipids to CD36, focusing on how this signaling cascade modulates foam cell formation, inflammatory responses, and metabolic pathways. An Administrative Core and 2 scientific cores, "Analytic and Synthetic Chemistry" and "Monocyte/Macrophage Cell Biology" strengthen the Program by providing well characterized, uniform-quality cellular, animal, and chemical reagents.
期刊论文(29)
专著(0)
科研奖励(0)
会议论文
DOI: 10.14800/ics.161
发表时间: 2014-06
期刊: Inflammation and cell signaling
影响因子: --
作者: [M. Cathcart;A. Bhattacharjee]
通讯作者: M. Cathcart;A. Bhattacharjee
Hematopoietic cell-restricted deletion of CD36 reduces high-fat diet-induced macrophage infiltration and improves insulin signaling in adipose tissue.
造血细胞限制性删除 CD36 可减少高脂饮食诱导的巨噬细胞浸润,并改善脂肪组织中的胰岛素信号传导。
DOI: 10.2337/db10-1353
发表时间: 2011-04
期刊: Diabetes
影响因子: 7.7
作者: [Nicholls HT, Kowalski G, Kennedy DJ, Risis S, Zaffino LA, Watson N, Kanellakis P, Watt MJ, Bobik A, Bonen A, Febbraio M, Lancaster GI, Febbraio MA]
通讯作者: Febbraio MA
DOI: 10.1161/atvbaha.113.302116
发表时间: 2014-01
期刊: Arteriosclerosis, thrombosis, and vascular biology
影响因子: --
作者: [Gupta N, Li W, Willard B, Silverstein RL, McIntyre TM]
通讯作者: McIntyre TM
DOI: 10.4049/jimmunol.1002710
发表时间: 2011-03-01
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者: [Chen R, Brady E, McIntyre TM]
通讯作者: McIntyre TM
22
    Hypertension augmented COVID-19 through renin-induced internalization of platelet-ACE2 / SARS-Cov-2 complexes
    • 批准号:
      10490385
    • 项目类别:
    • 资助金额:
      $57.23万
    • 财政年份:
      2021
    • 负责人:
      Thomas M McIntyre
    • 依托单位:
    Hypertension augmented COVID-19 through renin-induced internalization of platelet-ACE2 / SARS-Cov-2 complexes
    • 批准号:
      10275251
    • 项目类别:
    • 资助金额:
      $57.23万
    • 财政年份:
      2021
    • 负责人:
      Thomas M McIntyre
    • 依托单位:
    Pilot Project Core
    • 批准号:
      10397511
    • 项目类别:
    • 资助金额:
      $8.96万
    • 财政年份:
      2016
    • 负责人:
      Thomas M McIntyre
    • 依托单位:
    Core D: Pilot Project Core
    • 批准号:
      8977737
    • 项目类别:
    • 资助金额:
      $18.78万
    • 财政年份:
      2016
    • 负责人:
      Thomas M McIntyre
    • 依托单位:
    海外基金