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少突胶质细胞:生物学、免疫学及其与多发性硬化症的关系

The oligodendroglial cell: biology and immunology and relationship to multiple sclerosis.

作者信息

Bartlett P F, Mackay I R

出版信息

J Clin Lab Immunol. 1983 May;11(1):1-7.

PMID:6348293
Abstract

Myelin is elaborated and maintained in the central nervous system by the oligodendrocyte. The interaction between the oligodendrocyte and the neuron which initiates myelin formation is of major importance, and modern immunological technology using monoclonal antibodies and the fluorescence activated cell sorter have provided the means by which purified homogeneous populations of oligodendrocytes and neurons can be studied in vitro. The oligodendrocyte appears to have limited capacity to divide in situ which may contribute to the vulnerability of such cells in disease states; however it has been found that under certain culture conditions oligodendrocytes can proliferate in vitro. Multiple sclerosis (MS) is associated with loss of oligodendrocytes within the lesions and the intractability of the disease compared to other demyelinating conditions, both experimental and clinical, suggests, that the oligodendrocyte is the primary target of this disease. The cause of oligodendrocyte destruction is as yet uncertain although an immunological response may be in part responsible. The possible mechanism of immune recognition and cytolysis are discussed with regard to the unique nature of the nervous system.

摘要

少突胶质细胞在中枢神经系统中形成并维持髓鞘。少突胶质细胞与启动髓鞘形成的神经元之间的相互作用至关重要,而利用单克隆抗体和荧光激活细胞分选仪的现代免疫技术提供了在体外研究纯化的少突胶质细胞和神经元同质群体的方法。少突胶质细胞在原位似乎具有有限的分裂能力,这可能导致这些细胞在疾病状态下的易损性;然而,已经发现,在某些培养条件下,少突胶质细胞可以在体外增殖。多发性硬化症(MS)与病变内少突胶质细胞的丧失有关,与其他脱髓鞘疾病(包括实验性和临床性)相比,该疾病的难治性表明少突胶质细胞是这种疾病的主要靶点。少突胶质细胞破坏的原因尚不确定,尽管免疫反应可能部分起作用。关于神经系统的独特性质,讨论了免疫识别和细胞溶解的可能机制。

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