Role of PKCbeta in Diet-induced Hypercholesterolemia

PKCbeta 在饮食引起的高胆固醇血症中的作用

• 批准号: 7150032
• 负责人: KAMAL D MEHTA
• 金额: $ 28.35万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-12-06 至 2008-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7150032
• 关键词: Role; PKCbeta; Diet; induced; Hypercholesterolemia

DESCRIPTION (provided by applicant): Coronary artery disease (CAD) remains the leading cause of death and disability in our society. Of all known risk factors promoting CAD, a high serum level of low-density lipoprotein (LDL)-cholesterol is one of the most important risk factors. The plasma level of this lipoprotein is strongly influenced by genetic factors and the amount of dietary fat and cholesterol; dietary modification remains the cornerstone of CAD prevention. Our knowledge of the regulatory mechanism(s) controlling cholesterol homeostasis in response to dietary cholesterol is limited, as is the role of signaling pathways initiated by alterations in cholesterol levels. Also, the interrelationships between these signaling pathways and sterol response element-binding proteins (SREBPs), as well as the mechanism linking SREBP processing and cholesterol levels are not clear. The emerging picture from our work is that regulation of hepatic LDL receptors, crucial for cholesterol homeostasis, results from the activity of a few interlinked regulatory signaling pathways. We have previously shown, for the first-time, involvement of specific isoforms of protein kinase C (PKC) in the regulation of LDL receptor expression in cultured hepatic cells, possibly through direct modulation of activity by cholesterol. Based on our recent results, we propose a central role for B-isoform of PKC (PKCb) in regulating cholesterol homeostasis via modulating expression of selected genes crucial for this process. In Specific Aim 1, the role of PKCb in cholesterol homeostasis will be established by evaluating the effect of knockout of this ldnase on overall cholesterol homeostasis. Initial studies with PKC(-deficient mice strongly support a central role of this kinase in controlling the responsiveness of plasma cholesterol to the changes in the dietary cholesterol content. Cholesterol metabolism will be compared in detail between normal and PKCb mutants fed special diets. The Specific Aim 2 will compare expression of the hepatic genes critical for cholesterol homeostasis in the above animals. In Specific Aim 3, mechanisms by which PKCb affects SREBP-2 expression and its proteolytic processing, possibly by regulating INSIG- 1 phosphorylation will be examined. Finally, the nature of the isoform-specific interaction between cholesterol and PKCb will be examined in the Specific Aim 4. The photoactive cholesterol probe will be used to define at the molecular level structure(s) and amino acids that produce isoform-specific binding of PKCb to cholesterol. The proposed studies will not only establish the role of PKCb in diet-induced hypercholesterolemia, but will also identify genes regulated by this kinase, to correlate regulatory mechanisms to animal physiology. They will also help understand the complex interactions between environment and genetics leading to atherosclerosis. Accomplishment of the above aims will unravel a central signaling component that may act as a sensor to respond to dietary cholesterol; modulation of its activity may be the preferable mode for the treatment of lipid disorders in the 21st century.

描述(申请人提供)：冠状动脉疾病(CAD)仍然是我们社会中导致死亡和残疾的主要原因。在所有已知的促进冠心病的危险因素中，血清高水平的低密度脂蛋白-胆固醇是最重要的危险因素之一。这种脂蛋白的血浆水平受到遗传因素以及膳食脂肪和胆固醇含量的强烈影响；饮食调整仍然是预防冠心病的基石。我们对控制胆固醇稳态以响应饮食胆固醇的调节机制(S)的了解有限，胆固醇水平变化引发的信号通路的作用也是如此。此外，这些信号通路与固醇反应元件结合蛋白(SREBPs)之间的相互关系，以及SREBP加工与胆固醇水平之间的联系机制尚不清楚。从我们的工作中出现的情况是，对肝脏低密度脂蛋白受体的调节，对胆固醇稳态至关重要，是几个相互关联的调节信号通路活动的结果。我们以前首次发现，蛋白激酶C(PKC)的特定亚型参与调节培养的肝细胞中低密度脂蛋白受体的表达，可能是通过胆固醇直接调节活性。根据我们最近的研究结果，我们认为PKC的B-异构体(PKCb)在调节胆固醇动态平衡过程中的核心作用是通过调节在这一过程中至关重要的特定基因的表达。在具体目标1中，将通过评估敲除PKCb对总胆固醇稳态的影响来确定PKCb在胆固醇稳态中的作用。对PKC()缺陷小鼠的初步研究有力地支持了这种激酶在控制血浆胆固醇对饮食中胆固醇含量变化的反应性中的核心作用。胆固醇代谢将在正常和PKCb突变的特殊饮食中进行详细比较。特定的目标2将比较上述动物中对胆固醇稳态至关重要的肝脏基因的表达。在具体目标3中，将研究PKCb影响SREBP-2表达及其蛋白降解过程的机制，可能是通过调节INSIG-1的磷酸化。4.光活性胆固醇探针将被用来在分子结构(S)和产生同种异构体特异结合的氨基酸的分子水平上确定PKCb与胆固醇的结合。这项拟议的研究不仅将确定PKCb在饮食诱导的高胆固醇血症中的作用，还将确定由该激酶调控的基因，以将调控机制与动物生理联系起来。他们还将帮助理解导致动脉粥样硬化的环境和遗传之间的复杂相互作用。上述目标的实现将揭开一个可能作为对饮食胆固醇做出反应的传感器的中央信号成分；调节其活性可能是21世纪治疗血脂紊乱的首选模式。