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The circumventricular organs participate in the immunopathogenesis of experimental autoimmune encephalomyelitis

机译:室脑器官参与实验性自身免疫性脑脊髓炎的免疫发病机制

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Background During inflammatory conditions of the central nervous system (CNS), such as in multiple sclerosis or in its animal model, experimental autoimmune encephalomyelitis (EAE), immune cells migrate from the blood stream into the CNS parenchyma and into the cerebrospinal fluid (CSF) spaces. The endothelial blood-brain barrier (BBB) has been considered the most obvious entry site for circulating immune cells. Recently, the choroid plexus has been considered as an alternative entry site for circulating lymphocytes into the CSF. The choroid plexus, belongs to the circumventricular organs (CVOs) localized in the walls of the ventricles. Other CVOs, which similar to the choroid plexus lack an endothelial BBB, have not been considered as possible entry sites for immune cells into the CNS parenchyma or the CSF. Here we asked, whether CVOs are involved in the recruitment of inflammatory cells into the brain during EAE. Methods We performed an extensive immunohistological study on the area postrema (AP), the subfornical organ (SFO), the organum vasculosum of the lamina terminalis (OVLT) and the median eminence (ME) in frozen brain sections from healthy SJL mice and mice suffering from EAE. Expression of cell adhesion molecules, the presence of leukocyte subpopulations and the detection of major histocompatibility complex antigen expression was compared. Results Similar changes were observed for all four CVOs included in this study. During EAE significantly increased numbers of CD45+ leukocytes were detected within the four CVOs investigated, the majority of which stained positive for the macrophage markers F4/80 and Mac-1. The adhesion molecules ICAM-1 and VCAM-1 were upregulated on the fenestrated capillaries within the CVOs. A considerable upregulation of MHC class I throughout the CVOs and positive immunostaining for MHC class II on perivascular cells additionally documented the immune activation of the CVOs during EAE. A significant enrichment of inflammatory infiltrates was observed in close vicinity to the CVOs. Conclusion Our data indicate that the CVOs are a site for the entry of immune cells into the CNS and CSF and consequently are involved in the inflammatory process in the CNS during EAE.
机译:背景技术在中枢神经系统(CNS)的炎症状态下,例如多发性硬化症或其动物模型,实验性自身免疫性脑脊髓炎(EAE)中,免疫细胞从血流迁移到CNS实质和脑脊液(CSF)中空格。内皮血脑屏障(BBB)被认为是循环免疫细胞最明显的进入位点。最近,脉络丛被认为是使淋巴细胞循环进入脑脊液的另一种进入部位。脉络丛属于局部位于心室壁的室间隔器官(CVO)。类似于脉络丛的其他CVO缺乏内皮BBB,尚未被认为是免疫细胞进入中枢神经实质或CSF的可能进入位点。在这里,我们问,EAE期间CVO是否参与炎症细胞向大脑的募集。方法我们对来自健康SJL小鼠和患有SJL小鼠的冰冻脑切片中的区域后部区域(AP),分支下器官(SFO),椎板终末器官血管(OVLT)​​和中位隆起(ME)进行了广泛的免疫组织学研究。来自EAE。比较了细胞粘附分子的表达,白细胞亚群的存在和主要组织相容性复合物抗原表达的检测。结果本研究中包括的所有四个CVO均观察到类似的变化。在EAE期间,在所研究的四个CVO中检测到CD45 +白细胞的数量显着增加,其中大多数对巨噬细胞标记F4 / 80和Mac-1染色呈阳性。粘附分子ICAM-1和VCAM-1在CVO内的有孔毛细管上调。整个CVO中I类MHC的显着上调以及血管周细胞上MHC II类的阳性免疫染色还证明了EAE期间CVO的免疫激活。在靠近CVO的地方观察到大量炎性浸润。结论我们的数据表明CVOs是免疫细胞进入CNS和CSF的部位,因此参与了EAE期间CNS的炎症过程。

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