Deregulated lipid metabolism in stroke

中风中脂质代谢失调

• 批准号: 8072693
• 负责人: ROBERT J DEMPSEY
• 金额: $ 31.83万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8072693
• 关键词: 1,2-diacylglycerol; Abbreviations; Accounting; Address; Affect; Astrocytes; Attenuated; Brain Injuries; Cell Cycle; Cell Cycle Arrest; Cell Cycle Inhibition; Cell Cycle Proteins; Cell Cycle Regulation; Cell Proliferation; Cells; Ceramides; Cerebral Infarction; Cerebral Ischemia; Cessation of life; Clinical; Clinical Trials; Complement; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinases; Cyclins; Data; Development; Diglycerides; Enzymes; FDA approved; Fibroblast Growth Factor 2; Glucose; Health; Health Care Costs; Healthcare; Homeostasis; In Vitro; Inbred SHR Rats; Infarction; Interleukin-1; Knock-out; Lead; Lecithin; Lipids; Macrophage Activation; Mediating; Metabolism; Microglia; Middle Cerebral Artery Occlusion; Mitotic; Modeling; Neuroglia; Neurons; Oxygen; Palmitoyl Coenzyme A; Pathway interactions; Patients; Phase; Phospholipase C; Phosphorylation; Phosphorylcholine; Proliferating; Protein Dephosphorylation; Protein Phosphatase 2A Regulatory Subunit PR53; Protein phosphatase; Proteins; Rattus; Recovery; Recovery of Function; Regulation; Reperfusion Therapy; Research; Retinoblastoma; Scheme; Second Messenger Systems; Serine; Small Interfering RNA; Source; Sphingomyelinase; Sphingomyelins; Stroke; System; TNF gene; Testing; Therapeutic; Transient Cerebral Ischemia; Tumor Necrosis Factor-alpha; Up-Regulation; acidic sphingomyelinase; deprivation; disability; in vivo; inhibitor/antagonist; lipid metabolism; macrophage; neuronal survival; neuroprotection; oncoprotein p21; premature; prevent; protein kinase C zeta; public health relevance; research study; response; second messenger; serine palmitoyltransferase; sphingomyelin synthase; thermozymocidin; xanthate D609

DESCRIPTION (provided by applicant): Post-mitotic neurons can enter into the cell cycle after stroke but die instead of proliferating. Our data showed up- regulation of cyclin-dependent kinase 4 (Cdk4) after oxygen-glucose deprivation (OGD)/reoxygenation in near-pure primary cortical neuronal cultures, evidence of cell cycle entry. After cerebral ischemia, expressions of cell cycle proteins are altered. Inhibiting the cell cycle after stroke will provide benefit by attenuating neuronal death and proliferation of microglia/macrophages. Cell cycle regulation by lipid second messengers after stroke: Sphingomyelin (SM) synthase (SMS) transfers phosphocholine from phosphatidylcholine (PC) to ceramide to form SM and 1,2- diacylglycerol (DAG). Ceramide and DAG are key regulators of the cell cycle and altering their formation affects both neuronal and non-neuronal cell fate after stroke. Tricyclodecan-9-yl-xanthogenate (D609) inhibits SMS leading to ceramide accumulation. Ceramide can induce cell cycle arrest by (a) activating protein phosphatases 1 and 2A (PP1 and PP2A), (b) dephosphorylation of retinoblastoma (Rb) and Cdk2 and (c) up-regulation of Cdk inhibitors p21 and p27. Hypothesis: D609 may block the cell cycle, attenuating neuronal death and non-neuronal cell proliferation by increasing ceramide levels after stroke. The effect of D609 on ceramide de novo synthesis pathway will also be examined. In support of our hypothesis, D609 (a) significantly reduced cerebral infarction at reperfusion days 1 and 3, (b) up-regulated p21 and p27 through ceramide accumulation, and (c) attenuated Rb phosphorylation after transient middle cerebral artery occlusion (tMCAO) in rat. Our studies strongly support SMS inhibition by D609 leading to cell cycle arrest. To understand D609 mechanism, the following aims will test the hypothesis: Aim 1: Does D609 inhibit SMS, blocking the cell cycle and providing protection after OGD/reoxygenation in near-pure primary cortical neuronal cultures? Our studies showed that D609 up-regulated p27 in primary neuronal cultures after OGD/reoxygenation, suggesting increased ceramide due to SMS inhibition. Aim 2: How does SMS regulate cell cycle proteins and proliferation of RAW 264.7 macrophages? In vitro silencing of SMS (both in neuronal and macrophage cultures, Aims 1-2) will confirm the actions of D609 mediated through inhibition of SMS. Aim 3: How does D609 regulate SM metabolism, expression of cell cycle proteins, and microglia/macrophage proliferation in rat tMCAO? Our data suggest that D609 neuroprotection is due to increased ceramide levels, up-regulation of p21 and cell cycle arrest after tMCAO. Microglia/macrophages are the primary source of TNF-1 and IL-1 that are rapidly up-regulated after stroke and contribute to brain injury. We anticipate that D609 will reduce proliferation of microglia/macrophages as well as TNF-1 and IL-1ss expression after tMCAO, providing benefit. In vivo SMS silencing and SMS2 conditional (neuron-specific) knockout using cre/loxP system are proposed as alternatives. Translational potential: tPA has limited use in stroke patients. Although it is premature to predict, lipid metabolites that affect the cell cycle system in stroke have not been extensively studied and have not undergone stroke clinical trials. This proposal explores the therapeutic potential of D609 and how it affects lipid second messenger ceramide that regulates the cell cycle both in vitro and in vivo stroke models. PUBLIC HEALTH RELEVANCE: Stroke is a worldwide health care concern and a leading cause of disability. In the USA; healthcare costs are >$63 billion/year. Currently FDA approved tPA has a very limited use in stroke patients. The disappointing NXY-059 stroke clinical trials emphasized the need for new treatments. This research seeks to modulate a lipid metabolite by pharmacologically altering an enzyme system(s) that may offer benefit and may provide clues to develop lead molecules. The long-range thrust of this research is to develop strategies to minimize disabilities due to stroke.

描述（由申请人提供）：中风后有丝分裂后神经元可以进入细胞周期，但死亡而不是增殖。我们的数据显示，在近纯的原代皮层神经元培养物中，细胞周期蛋白依赖性激酶4 （Cdk4）在氧-葡萄糖剥夺(OGD)/再氧化后的调节，是细胞周期进入的证据。脑缺血后，细胞周期蛋白的表达发生改变。抑制中风后的细胞周期将通过减轻神经元死亡和小胶质细胞/巨噬细胞的增殖而受益。脑卒中后脂质第二信使对细胞周期的调控：鞘磷脂（SM）合成酶（SMS）将磷脂酰胆碱（PC）转化为神经酰胺形成SM和1,2-二酰基甘油（DAG）。神经酰胺和DAG是细胞周期的关键调节因子，改变它们的形成影响中风后神经元和非神经元细胞的命运。三环癸烷-9-基黄原酸（D609）抑制SMS导致神经酰胺积累。神经酰胺可以通过(a)激活蛋白磷酸酶1和2A (PP1和PP2A), (b)视网膜母细胞瘤（Rb）和Cdk2的去磷酸化以及(c) Cdk抑制剂p21和p27的上调诱导细胞周期阻滞。假设：D609可能通过增加脑卒中后神经酰胺水平，阻断细胞周期，减轻神经元死亡和非神经元细胞增殖。研究D609对神经酰胺新生合成途径的影响。为了支持我们的假设，D609 (a)在再灌注第1天和第3天显著减少脑梗死，(b)通过神经酰胺积累上调p21和p27， (c)在大鼠短暂性大脑中动脉闭塞（tMCAO）后减弱Rb磷酸化。我们的研究强烈支持D609抑制SMS导致细胞周期阻滞。为了了解D609的机制，以下目标将验证这一假设：目标1：在近纯原代皮层神经元培养物中，D609是否抑制SMS，阻断细胞周期并在OGD/再氧化后提供保护？我们的研究表明，D609在OGD/再氧化后的原代神经元培养中上调p27，表明由于SMS抑制而增加神经酰胺。目的2:SMS如何调节RAW 264.7巨噬细胞的细胞周期蛋白和增殖？体外沉默SMS（在神经元和巨噬细胞培养中，Aims 1-2）将证实D609通过抑制SMS介导的作用。目的3:D609如何调节大鼠tMCAO中SM代谢、细胞周期蛋白表达和小胶质细胞/巨噬细胞增殖？我们的数据表明，D609的神经保护作用是由于tMCAO后神经酰胺水平升高、p21上调和细胞周期阻滞。小胶质细胞/巨噬细胞是脑卒中后迅速上调的TNF-1和IL-1的主要来源，并有助于脑损伤。我们预计D609将减少tMCAO后小胶质细胞/巨噬细胞的增殖以及TNF-1和IL-1ss的表达，从而提供益处。建议使用cre/loxP系统进行体内SMS沉默和SMS2条件（神经元特异性）敲除。转化潜力：tPA在脑卒中患者中的应用有限。虽然现在预测还为时过早，但脂质代谢物对脑卒中细胞周期系统的影响尚未得到广泛研究，也未进行脑卒中临床试验。本研究旨在探讨D609在体外和体内中风模型中的治疗潜力，以及D609如何影响调节细胞周期的脂质第二信使神经酰胺。