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Role of cholesteryl ester transfer protein in cellular lipid homeostasis

Role of cholesteryl ester transfer protein in cellular lipid homeostasis
胆固醇酯转移蛋白在细胞脂质稳态中的作用
批准号:
8585078
负责人:
RICHARD E MORTON
金额:
$38.47万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-02-25 至 2015-11-30

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PROJECT SUMMARY/ABSTRACT Cholesteryl ester transfer protein (CETP) exchanges cholesteryl ester (CE) and triglyceride (TG) between lipoproteins and is well recognized as a regulator of plasma lipoprotein metabolism. CETP also resides inside cells where two isoforms exist: full-length (FL) and exon 9 (E9)-deleted CETP. The function of CETP inside cells is not understood, but it is clearly essential since inhibiting CETP biosynthesis in adipocytes impairs lipid storage. We postulate this occurs because intracellular CETP is required for CE and TG transport from their site of synthesis to their site of storage. To test this general hypothesis, we propose three specific aims. Aim 1 - Determine the CETP isoform(s) that promote cellular lipid storage, and define the structural features of CETP that are essential to its intracellular function. This aim tests the hypothesis that E9-deleted CETP facilitates intracellular lipid transport directly or by interacting with FL CETP, and also examines how this cellular activity depends on CETP structure. Aim 2 - Define the role of CETP in cellular lipid metabolism. To unravel the mechanisms by which CETP deficiency disrupts cellular lipid metabolism, this aim quantifies metabolic alterations and defines changes in lipid droplet formation that occur when CETP isoform expression is altered. Aim 3 - Define the role of CETP in the formation and utilization of lipid storage droplets in lipoprotein- synthesizing cells. Consistent with preliminary studies, we propose that in lipoprotein-synthesizing cells CETP assists in both lipid droplet formation and the reverse transport of stored lipids to microsomes for lipoprotein assembly. Genetic and adenoviral approaches will alter expression of FL and/or E9-deleted CETPs in SW872 adipocytes, Caco-2 intestinal enterocytes, and in hamster. The consequences of these molecular manipulations on lipid synthesis, interorganelle lipid transport, lipid droplet formation and lipoprotein assembly will be studied through biochemical and microscopy techniques. These studies will describe a novel function for CETP and advance our understanding of cellular lipid transport and storage mechanisms. Lipid storage in adipocytes is linked to their secretion of hormones that regulate glucose and lipid metabolism, which directly affect processes such as inflammation and atherogenesis.
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Partial suppression of CETP activity beneficially modifies the lipid transfer profile of plasma.
部分抑制 CETP 活性有利于改变血浆的脂质转移曲线。
DOI: 10.1016/j.atherosclerosis.2006.06.030
发表时间: 2007
期刊: Atherosclerosis
影响因子: 5.3
作者: [Morton,RichardE, Greene,DianeJ]
通讯作者: Greene,DianeJ
DOI: 10.1194/jlr.m100431-jlr200
发表时间: 2002-08-01
期刊: JOURNAL OF LIPID RESEARCH
影响因子: 6.5
作者: [Skeggs, JW, Morton, RE]
通讯作者: Morton, RE
The capacity of various non-esterified fatty acids to suppress lipid transfer inhibitor protein activity is related to their perturbation of the lipoprotein surface.
各种非酯化脂肪酸抑制脂质转移抑制剂蛋白活性的能力与其对脂蛋白表面的扰动有关。
DOI: 10.1016/s1388-1981(00)00064-0
发表时间: 2000
期刊: Biochimica et biophysica acta
影响因子: --
作者: [Morton,RE, Greene,DJ]
通讯作者: Greene,DJ
CETP and lipid transfer inhibitor protein are uniquely affected by the negative charge density of the lipid and protein domains of LDL.
CETP 和脂质转移抑制蛋白独特地受到 LDL 脂质和蛋白质结构域负电荷密度的影响。
DOI: 10.1194/jlr.m300171-jlr200
发表时间: 2003
期刊: Journal of lipid research
影响因子: 6.5
作者: [Morton,RichardE, Greene,DianeJ]
通讯作者: Greene,DianeJ
Apolipoprotein F enhances HDL function
  • 批准号:
    9236396
  • 项目类别:
  • 资助金额:
    $39.63万
  • 财政年份:
    2016
  • 负责人:
    RICHARD E MORTON
  • 依托单位:
CORE C-- LIPOPROTEIN AND ATHEROSCLEROSIS
  • 批准号:
    6921890
  • 项目类别:
  • 资助金额:
    $8.97万
  • 财政年份:
    2004
  • 负责人:
    RICHARD E MORTON
  • 依托单位:
CORE -- LIPOPROTEIN AND ATHEROSCLEROSIS
  • 批准号:
    6770261
  • 项目类别:
  • 资助金额:
    $8.66万
  • 财政年份:
    2003
  • 负责人:
    RICHARD E MORTON
  • 依托单位:
CORE--LIPOPROTEIN
  • 批准号:
    6327702
  • 项目类别:
  • 资助金额:
    $19.21万
  • 财政年份:
    2000
  • 负责人:
    RICHARD E MORTON
  • 依托单位:
国内基金
海外基金
支链氨基酸代谢紊乱调控“Adipocytes - Macrophages Crosstalk”诱发2型糖尿病脂肪组织功能和结构障碍的作用及机制