Deregulated lipid metabolism in stroke

中风中脂质代谢失调

• 批准号: 8477320
• 负责人: ROBERT J DEMPSEY
• 金额: $ 30.72万
• 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 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8477320
• 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.

描述(申请人提供)：卒中后有丝分裂后神经元可以进入细胞周期，但会死亡而不是增殖。我们的数据显示，在近纯的原代皮质神经元培养中，缺氧-葡萄糖剥夺(OGD)/复氧后细胞周期蛋白依赖性激酶4(CDK4)表达上调，这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。卒中后脂质第二信使对细胞周期的调节：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，改变它们的形成会影响中风后神经细胞和非神经细胞的命运。三环十二烷-9-基黄原酸酯(D609)可抑制SMS，导致神经酰胺蓄积。神经酰胺可通过(A)激活蛋白磷酸酶1和2A(PP1和PP2A)，(B)使视网膜母细胞瘤(Rb)和CDK2去磷酸化，以及(C)上调CDK抑制剂p21和p27来诱导细胞周期停滞。假设：D609可能通过增加卒中后神经酰胺水平而阻断细胞周期，减轻神经元死亡和非神经元细胞增殖。D609对神经酰胺从头合成途径的影响也将被检测。为了支持我们的假设，D609(A)显著减少再灌注第1天和第3天的脑梗塞，(B)通过神经酰胺堆积上调p21和p27的表达，以及(C)减弱短暂大脑中动脉闭塞(TMCAO)后Rb的磷酸化。我们的研究有力地支持了D609对短信的抑制作用，导致细胞周期停滞。为了理解D609的机制，以下目的将检验这一假设：目的1：在近纯的原代皮层神经元培养中，D609是否抑制SMS，阻断细胞周期，并在OGD/复氧后提供保护？我们的研究表明，D609在OGD/复氧后上调原代神经元培养中p27的表达，提示Sms抑制导致神经酰胺增加。目的2：丹参如何调节细胞周期蛋白和RAW 264.7巨噬细胞的增殖？Sms的体外沉默(在神经元和巨噬细胞培养中，AIMS 1-2)将证实D609通过抑制Sm介导的作用。目的3：D609是如何调节大鼠大脑中动脉阻塞时SM代谢、细胞周期蛋白表达及小胶质细胞/巨噬细胞增殖的？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上调和细胞周期停滞所致。小胶质细胞/巨噬细胞是肿瘤坏死因子-1和白介素1的主要来源，它们在中风后迅速上调，并导致脑损伤。我们预计D609将减少TMCAO后小胶质细胞/巨噬细胞的增殖以及肿瘤坏死因子-1和白介素1-SS的表达，从而提供有益的帮助。体内的短信沉默和使用cre/loxP系统的SMS2条件性(神经元特异性)基因敲除被提出作为替代方案。翻译潜力：TPA在中风患者中的使用有限。尽管预测还为时过早，但影响中风细胞循环系统的脂代谢产物尚未得到广泛研究，也未进行中风临床试验。这项建议探索了D609的治疗潜力以及它如何在体外和体内中风模型中影响调节细胞周期的脂质第二信使神经酰胺。

项目成果

Tricyclodecan-9-yl-xanthogenate (D609) mechanism of actions: a mini-review of literature.

• DOI: 10.1007/s11064-011-0659-z
• 发表时间: 2012-04
• 期刊: NEUROCHEMICAL RESEARCH
• 影响因子: 4.4
• 作者: Adibhatla, Rao Muralikrishna;Hatcher, J. F.;Gusain, A.
• 通讯作者: Gusain, A.

Distinction between phosphatidylcholine (PC)-specific phospholipase C (PC-PLC) and phosphatidylinositol (PI)-specific phospolipase C (PI-PLC) needs clarification.

磷脂酰胆碱 (PC) 特异性磷脂酶 C (PC-PLC) 和磷脂酰肌醇 (PI) 特异性磷脂酶 C (PI-PLC) 之间的区别需要澄清。

• DOI: 10.1016/j.bbrc.2012.02.010
• 发表时间: 2012
• 期刊: Biochemical and biophysical research communications
• 影响因子: 3.1
• 作者: Adibhatla,RaoMuralikrishna

Sphingomyelin Synthase 1 Regulates Neuro-2a Cell Proliferation and Cell Cycle Progression Through Modulation of p27 Expression and Akt Signaling.

• DOI: 10.1007/s12035-014-8829-z
• 发表时间: 2015
• 期刊: MOLECULAR NEUROBIOLOGY
• 影响因子: 5.1
• 作者: Wesley, Umadevi V.;Hatcher, James F.;Dempsey, Robert J.
• 通讯作者: Dempsey, Robert J.

Erratum to: Anti-proliferative Effects of Tricyclodecan-9-yl-xanthogenate (D609) Involve Ceramide and Cell Cycle Inhibition.

勘误表：Tricyclodecan-9-yl-xantogenate (D609) 的抗增殖作用涉及神经酰胺和细胞周期抑制。

• 发表时间: 2012
• 期刊: Molecular neurobiology
• 影响因子: 5.1
• 作者: Gusain,Anchal;Hatcher,JamesF;Adibhatla,RaoMuralikrishna;Wesley,UmadeviV;Dempsey,RobertJ
• 通讯作者: Dempsey,RobertJ

Anti-proliferative effects of tricyclodecan-9-yl-xanthogenate (D609) involve ceramide and cell cycle inhibition.

• DOI: 10.1007/s12035-012-8254-0
• 发表时间: 2012-06
• 期刊: MOLECULAR NEUROBIOLOGY
• 影响因子: 5.1
• 作者: Gusain, Anchal;Hatcher, James F.;Adibhatla, Rao Muralikrishna;Wesley, Umadevi V.;Dempsey, Robert J.
• 通讯作者: Dempsey, Robert J.