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少突胶质前体细胞向少突胶质细胞的分化与Ia抗原诱导性的丧失有关。

The differentiation of O-2A progenitor cells into oligodendrocytes is associated with a loss of inducibility of Ia antigens.

作者信息

Calder V L, Wolswijk G, Noble M

机构信息

Department of Neurochemistry, Institute of Neurology, London, GB.

出版信息

Eur J Immunol. 1988 Aug;18(8):1195-201. doi: 10.1002/eji.1830180808.

Abstract

Current data suggest that some astrocytes, one of the 3 main types of macroglia in the central nervous system (CNS), can be induced by interferon-gamma (IFN-gamma) to express major histocompatibility complex class II antigens (immune-associated or Ia) and present antigen to T lymphocytes. In contrast, oligodendrocytes, another type of macroglia, cannot be induced to express Ia. The astrocytes which have been shown to express Ia are from a particular glial lineage and are called type-1 astrocytes. The oligodendrocyte-type-2 astrocyte (O-2A) lineage, which gives rise to oligodendrocytes, also gives rise to a second class of astrocytes called type-2 astrocytes and the ability of type-2 astrocytes or the common O-2A progenitor cell to express Ia is not known. We have now found that both type-2 astrocytes and O-2A progenitor cells can be induced to express Ia by IFN-gamma but Ia expression is not induced in oligodendrocytes in parallel cultures. Thus, it appears that differentiation of O-2A progenitor cells into oligodendrocytes is specifically associated with a loss of inducibility of Ia. This apparent loss of the capacity for Ia expression, and presumably antigen presentation, in oligodendrocytes (the cells which produce myelin in the CNS) is of particular interest in view of the ability of immunization of myelin components to produce autoimmune-mediated paralytic disease.

摘要

目前的数据表明,星形胶质细胞作为中枢神经系统(CNS)中3种主要的大胶质细胞类型之一,可被γ干扰素(IFN-γ)诱导表达主要组织相容性复合体II类抗原(免疫相关或Ia),并将抗原呈递给T淋巴细胞。相比之下,少突胶质细胞作为另一种大胶质细胞类型,不能被诱导表达Ia。已被证明表达Ia的星形胶质细胞来自特定的神经胶质谱系,被称为1型星形胶质细胞。少突胶质细胞-2型星形胶质细胞(O-2A)谱系可产生少突胶质细胞,也可产生另一类被称为2型星形胶质细胞的星形胶质细胞,而2型星形胶质细胞或常见的O-2A祖细胞表达Ia的能力尚不清楚。我们现在发现,2型星形胶质细胞和O-2A祖细胞均可被IFN-γ诱导表达Ia,但在平行培养的少突胶质细胞中未诱导出Ia表达。因此,似乎O-2A祖细胞向少突胶质细胞的分化与Ia诱导性的丧失特别相关。鉴于免疫髓磷脂成分会产生自身免疫介导的麻痹性疾病,少突胶质细胞(中枢神经系统中产生髓磷脂的细胞)中Ia表达能力以及推测的抗原呈递能力的明显丧失尤其令人关注。

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