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Activation of pial and dural macrophages and dendritic cells by cortical spreading depression

机译:通过皮质扩散抑制激活小毛细血管和硬化巨噬细胞和树突细胞

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摘要

Objective Cortical spreading depression (CSD) has long been implicated in migraine attacks with aura. The process by which CSD, a cortical event that occurs within the blood–brain barrier (BBB), results in nociceptor activation outside the BBB is likely mediated by multiple molecules and cells. The objective of this study was to determine whether CSD activates immune cells inside the BBB (pia), outside the BBB (dura), or in both, and if so, when. Methods Investigating cellular events in the meninges shortly after CSD, we used in vivo two‐photon imaging to identify changes in macrophages and dendritic cells (DCs) that reside in the pia, arachnoid, and dura and their anatomical relationship to TRPV1 axons. Results We found that activated meningeal macrophages retract their processes and become circular, and that activated meningeal DCs stop migrating. We found that CSD activates pial macrophages instantaneously, pial, subarachnoid, and dural DCs 6‐12 minutes later, and dural macrophages 20 minutes later. Dural macrophages and DCs can appear in close proximity to TRPV1‐positive axons. Interpretation The findings suggest that activation of pial macrophages may be more relevant to cases where aura and migraine begin simultaneously, that activation of dural macrophages may be more relevant to cases where headache begins 20 to 30 minutes after aura, and that activation of dural macrophages may be mediated by activation of migratory DCs in the subarachnoid space and dura. The anatomical relationship between TRPV1‐positive meningeal nociceptors, and dural macrophages and DCs supports a role for these immune cells in the modulation of head pain. Ann Neurol 2018;83:508–521
机译:目的皮质蔓延抑郁症(CSD)长期以来一直涉及与光环的偏头痛攻击。 CSD,发生在血脑屏障(BBB)内发生的皮质事件的过程导致BBB外部的伤虫活化可能由多个分子和细胞介导。本研究的目的是确定CSD是否在BBB(PIA)外,在BBB(DURA)外,或两者,如果是的话,何时。方法在CSD后不久,在CSD后不久研究脑膜细胞事件,用于鉴定巨噬细胞和树突状细胞(DCS)的变化,其与TRPV1轴突中的巨噬细胞和树突状细胞(DCS)的变化及其解剖关系。结果我们发现激活的脑膜巨噬细胞缩回它们的过程并变得圆形,并且激活的脑病DCS停止迁移。我们发现CSD瞬间,小植物,蛛网膜下腔和多噬细胞6-12分钟后激活小植物,并且在后续20分钟后巨噬细胞。 Dural巨噬细胞和DCS可以靠近TRPV1阳性轴突。解释结果表明,小巨噬细胞的激活可能与Aura和偏头痛同时开始的病例更相关,这种情况可能与心疼后20至30分钟的病例更相关,并且激活多云巨噬细胞可能通过在蛛网膜下腔空间和硬脑膜瘤中的迁移DC激活来介导。 TRPV1阳性脑膜肌肌蛋白和多噬细胞和DC之间的解剖关系支持这些免疫细胞在头痛调节中的作用。 Ann Neurol 2018; 83:508-521

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  • 来源
    《Annals of neurology》 |2018年第3期|共14页
  • 作者单位

    Department of AnesthesiaCritical Care and Pain Medicine Beth Israel Deaconess Medical CenterBoston;

    Department of AnesthesiaCritical Care and Pain Medicine Beth Israel Deaconess Medical CenterBoston;

    Harvard Medical SchoolBoston MA;

    Department of Neurology Department of NeuroscienceYale School of MedicineNew Haven CT;

    Department of AnesthesiaCritical Care and Pain Medicine Beth Israel Deaconess Medical CenterBoston;

    Department of AnesthesiaCritical Care and Pain Medicine Beth Israel Deaconess Medical CenterBoston;

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  • 正文语种 eng
  • 中图分类 神经病学;
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