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Neurotoxic reactive astrocytes are induced by activated microglia

机译:活化的小胶质细胞诱导神经毒性反应性星形胶质细胞

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摘要

Reactive astrocytes are strongly induced by central nervous system (CNS) injury and disease, but their role is poorly understood. Here we show that a subtype of reactive astrocytes, which we termed A1, is induced by classically activated neuroinflammatory microglia. We show that activated microglia induce A1 astrocytes by secreting Il-1 alpha, TNF and C1q, and that these cytokines together are necessary and sufficient to induce A1 astrocytes. A1 astrocytes lose the ability to promote neuronal survival, outgrowth, synaptogenesis and phagocytosis, and induce the death of neurons and oligodendrocytes. Death of axotomized CNS neurons in vivo is prevented when the formation of A1 astrocytes is blocked. Finally, we show that A1 astrocytes are abundant in various human neurodegenerative diseases including Alzheimer's, Huntington's and Parkinson's disease, amyotrophic lateral sclerosis and multiple sclerosis. Taken together these findings help to explain why CNS neurons die after axotomy, strongly suggest that A1 astrocytes contribute to the death of neurons and oligodendrocytes in neurodegenerative disorders, and provide opportunities for the development of new treatments for these diseases.
机译:反应性星形胶质细胞是由中枢神经系统(CNS)损伤和疾病强烈诱导的,但对其作用了解甚少。在这里,我们显示了经典激活的神经炎症小胶质细胞诱导的一种反应性星形胶质细胞亚型,我们称为A1。我们显示激活的小胶质细胞通过分泌Il-1 a​​lpha,TNF和C1q诱导A1星形胶质细胞,并且这些细胞因子在一起是诱导A1星形胶质细胞的必要和充分条件。 A1星形胶质细胞丧失了促进神经元存活,生长,突触形成和吞噬作用的能力,并诱导神经元和少突胶质细胞的死亡。当A1星形胶质细胞的形成被阻止时,可以防止体内被轴突切除的CNS神经元的死亡。最后,我们显示A1星形胶质细胞在各种人类神经退行性疾病中丰富,包括阿尔茨海默氏病,亨廷顿氏病和帕金森氏病,肌萎缩性侧索硬化症和多发性硬化症。综合这些发现,有助于解释为什么中枢神经系统神经元在轴突切开术后死亡,强烈暗示A1星形胶质细胞有助于神经退行性疾病中神经元和少突胶质细胞的死亡,并为开发针对这些疾病的新疗法提供了机会。

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  • 来源
    《Nature》 |2017年第7638期|481-487|共7页
  • 作者单位

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA|Univ Melbourne, Dept Pharmacol & Therapeut, Parkville, Vic 3010, Australia;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA|Stanford Univ, Dept Psychiat & Behav Sci, Sch Med, Stanford, CA 94305 USA;

    Univ Melbourne, Dept Pharmacol & Therapeut, Parkville, Vic 3010, Australia;

    Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA|Tech Univ Munich, Dept Neurol, Klinikum Rechts Isar, D-81675 Munich, Germany;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA;

    Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 34141, South Korea;

    Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA;

    Boston Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA;

    Boston Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA;

    Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA;

    Johns Hopkins Univ, Sch Med, Neuroregenerat Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Stem Cell Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA|Adrienne Helis Malvin Med Res Fdn, New Orleans, LA 70130 USA;

    Johns Hopkins Univ, Sch Med, Neuroregenerat Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Stem Cell Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA|Adrienne Helis Malvin Med Res Fdn, New Orleans, LA 70130 USA;

    Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA;

    Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA|Univ Calif San Francisco, Dept Neurosurg, San Francisco, CA 94143 USA|Univ Cambridge, Dept Paediat, Cambridge CB2, England;

    Johns Hopkins Univ, Sch Med, Neuroregenerat Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Stem Cell Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA|Adrienne Helis Malvin Med Res Fdn, New Orleans, LA 70130 USA|Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA;

    Johns Hopkins Univ, Sch Med, Neuroregenerat Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Stem Cell Program, Inst Cell Engn, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA|Adrienne Helis Malvin Med Res Fdn, New Orleans, LA 70130 USA|Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA|Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA;

    Boston Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA;

    Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA;

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