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Multiple Sclerosis Is A Neurodegeneration Specifically Targeting Oligodendrocytes and Myelin Sheaths

机译:多发性硬化症是专门针对少突胶质细胞和髓鞘的神经变性。

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Considerations regarding pathogenesis of multiple sclerosis plaques would revolve around heterogeneous modes of involvement of a central venule in the ongoing progression of relapsing/remitting demyelination and of axonal loss. Neurodegeneration of the parent neuron appears pivotal as a demyelinating /remyelinating series of events borne out by the inflammatory nature of the lesions, the multiple sclerosis plaques. Implied involvement of inflammatory and immune cell elements might help account for modes of progression of an ischemic lesion that targets the oligodendrocyte with loss of its myelin sheath around multiple independent segments of an integral axon. Indeed, multiple sclerosis proves a neurodegenerative state that progresses as a demyelination of segmental axonal involvement and of individual oligodendrocytes around specific venules of supply.
机译:关于多发性硬化斑块的发病机理的考虑将围绕中央小静脉参与复发/缓解脱髓鞘和轴突丧失的进行中的异质参与模式。母体神经元的神经退行性变是关键性的,是一系列由病变的炎症性质,多发性硬化斑块证实的脱髓鞘/再髓鞘事件。暗示性的炎症和免疫细胞因子的参与可能有助于解释缺血性病变的发展模式,该病变以少突胶质细胞为靶点,其髓鞘的缺失围绕着完整轴突的多个独立部分。实际上,多发性硬化症证明是神经退行性状态,其随着节段性轴突受累以及特定供应小静脉周围的单个少突胶质细胞的脱髓鞘而发展。

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