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小胶质细胞在吞噬少突胶质细胞后将髓鞘抗原呈递给T细胞。

Microglia present myelin antigens to T cells after phagocytosis of oligodendrocytes.

作者信息

Cash E, Zhang Y, Rott O

机构信息

Department of Neuroimmunology, Max-Planck Institute for Psychiatry, Martinsried-Munich, Germany.

出版信息

Cell Immunol. 1993 Mar;147(1):129-38. doi: 10.1006/cimm.1993.1053.

Abstract

Cells that are capable of initiating immune reactions in the central nervous system (CNS) seem to be microglia, since they are the predominant CNS cell type expressing major histocompatibility complex (MHC) class II molecules. However, the capacity of microglia to induce myelin antigen-specific T lymphocyte activation is not yet well defined. With a coculture system allowing phagocytosis by microglia of progenitor or mature oligodendrocytes (synthesizing myelin basic protein, MBP), we show the ability of phagocytosis-activated microglia to express MHC class II antigen and to strongly induce T cell proliferation. The T cell proliferation was either mitogen mediated or antigen specific (MBP). Activation of microglia by phagocytosis may represent a major step in initializing immune responses in the CNS.

摘要

能够在中枢神经系统(CNS)引发免疫反应的细胞似乎是小胶质细胞,因为它们是中枢神经系统中表达主要组织相容性复合体(MHC)II类分子的主要细胞类型。然而,小胶质细胞诱导髓鞘抗原特异性T淋巴细胞激活的能力尚未明确界定。通过一种共培养系统,该系统允许小胶质细胞吞噬祖细胞或成熟少突胶质细胞(合成髓鞘碱性蛋白,MBP),我们展示了吞噬激活的小胶质细胞表达MHC II类抗原并强烈诱导T细胞增殖的能力。T细胞增殖要么是有丝分裂原介导的,要么是抗原特异性的(MBP)。吞噬作用激活小胶质细胞可能是启动中枢神经系统免疫反应的一个主要步骤。

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