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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Inducible nitric oxide synthase in chronic active multiple sclerosis plaques: distribution, cellular expression and association with myelin damage.
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Inducible nitric oxide synthase in chronic active multiple sclerosis plaques: distribution, cellular expression and association with myelin damage.

机译:慢性活动性多发性硬化斑块中的诱导型一氧化氮合酶:分布,细胞表达以及与髓磷脂损伤的相关性。

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Inducible nitric oxide synthase (iNOS) is an enzyme that produces nitric oxide (NO) and is thought to contribute to the pathogenesis of multiple sclerosis (MS). The extent of iNOS expression was examined using laser scanning confocal microscopy of 13 chronic active plaques from seven MS patients displaying both acute demyelination and active inflammation. iNOS expression in these plaques was substantial and diverse in cellular distribution. Expression of iNOS was observed in ependymal cells located in periventricular lesions, inflammatory cells, and occasionally in astrocytes. iNOS was found in microglial/macrophage cells that expressed CD64, the high affinity Fcgamma receptor associated with cells that have phagocytic function and participate in antibody-dependent cellular cytotoxicity (ADCC). Scavenger microglial/macrophage cells that expressed the marker CD14 were also present and may express iNOS. The markers for myelin damage, nitrotyrosine (an index of iNOS mediated damage via peroxynitrite formation), along with MBP fragments, were also observed associated with iNOS in MS plaques. Together, these findings support a central role for iNOS in the pathogenesis of multiple sclerosis.
机译:诱导型一氧化氮合酶(iNOS)是一种产生一氧化氮(NO)的酶,被认为与多发性硬化症(MS)的发病机理有关。 iNOS表达的程度使用激光扫描共聚焦显微镜检查了7名MS患者的13个慢性活动性斑块,这些斑块均显示了急性脱髓鞘和活动性炎症。这些斑块中的iNOS表达在细胞分布中是实质性的并且是多样的。在位于脑室周围病变的室管膜细胞,炎性细胞中,偶尔在星形胶质细胞中观察到iNOS的表达。 iNOS在表达CD64的小胶质细胞/巨噬细胞中发现,CD64是与具有吞噬功能并参与抗体依赖性细胞毒性(ADCC)的细胞相关的高亲和力Fcγ受体。还存在表达标记物CD14的清道夫小胶质细胞/巨噬细胞,并且可能表达iNOS。还观察到髓磷脂损伤的标志物,硝基酪氨酸(iNOS介导的过氧亚硝酸盐形成引起的损伤指数)以及MBP片段与MS斑块中的iNOS相关。总之,这些发现支持iNOS在多发性硬化症发病机制中的重要作用。

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