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首页> 外文期刊>Brain pathology >Elevated activity and microglial expression of myeloperoxidase in demyelinated cerebral cortex in multiple sclerosis.
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Elevated activity and microglial expression of myeloperoxidase in demyelinated cerebral cortex in multiple sclerosis.

机译:多发性硬化症脱髓鞘性大脑皮层中髓过氧化物酶的活性和小胶质细胞表达增加。

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摘要

Recent studies have revealed extensive cortical demyelination in patients with progressive multiple sclerosis (MS). Demyelination in gray matter lesions is associated with activation of microglia. Macrophages and microglia are known to express myeloperoxidase (MPO) and generate reactive oxygen species during myelin phagocytosis in the white matter. In the present study we examined the extent of microglial activation in the cerebral cortex and the relationship of microglial activation and MPO activity to cortical demyelination. Twenty-one cases of neuropathologically confirmed multiple sclerosis, with 34 cortical lesions, were used to assess microglial activation. HLA-DR immunolabeling of activated microglia was significantly higher in demyelinated MS cortex than control cortex and, within the MS cohort, was significantly greater within cortical lesions than in matched non-demyelinated areas of cortex. In homogenates of MS cortex, cortical demyelination was associated with significantly elevated MPO activity. Immunohistochemistry revealed MPO in CD68-positive microglia within cortical plaques, particularly toward the edge of the plaques, but not in microglia in adjacent non-demyelinated cortex. Cortical demyelination in MS is associated with increased activity of MPO, which is expressed by a CD68-positive subset of activated microglia, suggesting that microglial production of reactive oxygen species is likely to be involved in cortical demyelination.
机译:最近的研究表明,进行性多发性硬化症(MS)患者广泛的皮质脱髓鞘。灰质病变中的脱髓鞘与小胶质细胞的激活有关。已知巨噬细胞和小胶质细胞表达髓过氧化物酶(MPO),并在白质的髓磷脂吞噬过程中产生活性氧。在本研究中,我们检查了大脑皮层中小胶质细胞活化的程度以及小胶质细胞活化和MPO活性与皮层脱髓鞘的关系。 21例经神经病理学证实为多发性硬化症的病例,其中有34个皮层病变,用于评估小胶质细胞的激活。在脱髓鞘的MS皮层中,活化小胶质细胞的HLA-DR免疫标记显着高于对照皮层,而在MS队列中,皮层病变内的皮层中,与匹配的非脱髓鞘区域相比,其显着更高。在MS皮层匀浆中,皮层脱髓鞘与MPO活性显着升高有关。免疫组化显示皮质斑块内CD68阳性小胶质细胞中的MPO,尤其是朝向斑块边缘的MPO,但在相邻的非脱髓鞘皮质的小胶质细胞中则没有。 MS中的皮质脱髓鞘与MPO活性增加有关,MPO活性由活化的小胶质细胞的CD68阳性子集表达,表明活性神经胶质的小胶质细胞产生可能与皮质脱髓鞘有关。

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