首页> 外文期刊>American Journal of Pathology >The Low-Density Lipoprotein Receptor-Related Protein 1 Mediates Tissue-Type Plasminogen Activator-Induced Microglial Activation in the Ischemic Brain
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The Low-Density Lipoprotein Receptor-Related Protein 1 Mediates Tissue-Type Plasminogen Activator-Induced Microglial Activation in the Ischemic Brain

机译:低密度脂蛋白受体相关蛋白1介导缺血性脑组织型纤溶酶原激活物诱导的小胶质细胞活化。

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摘要

Microglia are the immune cells of the central nervous system (CNS) that become activated in response to pathological situations such as cerebral ischemia. Tissue-type plasminogen activator (tPA) is a serine proteinase that is found in the intravascular space and the CNS. The low-density lipoprotein receptor-related protein 1 (LRP1) is a member of the low-density lipoprotein receptor gene family found in neurons, astrocytes, and microglia. The present study investigated whether the interaction between tPA and microglial LRP1 plays a role in cerebral ischemia-induced microglial activation. We found that middle cerebral artery occlusion (MCAO) induces microglial activation in both wild-type and plasminogen-deficient (Plg–/–) mice. In contrast, MCAO-induced microglial activation is significantly decreased in tPA-deficient (tPA–/–) mice and in mice that lack LRP1 in microglial cells (macLRP–). We observed a significant increase in microglial activation when tPA–/– mice received treatment with murine tPA after MCAO. In contrast, treatment of macLRP– mice with tPA did not have an effect on the extent of microglial activation. Finally, both the volume of the ischemic lesion as well as inducible nitric oxide synthase production were significantly decreased in macLRP– mice and macLRP– microglia. In summary, our results indicate that the interaction between tPA and LRP1 induces microglial activation with the generation of an inflammatory response in the ischemic brain, suggesting a cytokine-like role for tPA in the CNS.
机译:小胶质细胞是中枢神经系统 (CNS)的免疫细胞,可响应诸如脑缺血等病理情况 而被激活。组织型纤溶酶原激活物 (tPA)是一种丝氨酸蛋白酶,存在于血管内 空间和CNS中。低密度脂蛋白受体相关蛋白 蛋白1(LRP1)是神经元,星形胶质细胞和小胶质细胞中发现的低密度脂蛋白受体基因家族的成员。 > 本研究调查了 tPA和小胶质LRP1之间的相互作用是否在脑缺血诱导的 小胶质细胞激活中起作用。我们发现大脑中动脉 闭塞(MCAO)在野生型 和纤溶酶原缺陷型(Plg – / – )小鼠中均诱导小胶质细胞活化。相反,在tPA缺陷(tPA – / – )小鼠和小鼠中, MCAO诱导的小胶质细胞活化显着降低了 小胶质细胞中缺少LRP1(macLRP – )。当tPA – / – 小鼠接受MCAO后接受鼠tPA治疗时,我们观察到小胶质细胞活化显着增加。相反,用tPA 处理macLRP – 小鼠对小胶质细胞活化程度没有影响。最后,在macLRP – 小鼠 中,缺血性病变的体积 以及诱导型一氧化氮合酶 的产生均显着降低。 sup>和macLRP – 小胶质细胞。总之,我们的结果表明 tPA和LRP1之间的相互作用诱导小胶质细胞 活化,并在缺血性脑中产生炎症反应,这表明tPA 在中枢神经系统中的细胞因子样作用。

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  • 来源
    《American Journal of Pathology》 |2009年第2期|586-594|共9页
  • 作者单位

    From the Department of Neurology and Center for Neurodegenerative Disease,Emory University School of Medicine, Atlanta, Georgia;

    From the Department of Neurology and Center for Neurodegenerative Disease,Emory University School of Medicine, Atlanta, Georgia|the Institute of Pharmacology,Shandong University School of Medicine, Jinan, China;

    and the Center for Vascular and Inflammatory Diseases,the University of Maryland School of Medicine, Baltimore, Maryland;

    From the Department of Neurology and Center for Neurodegenerative Disease,Emory University School of Medicine, Atlanta, Georgia;

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