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Axonal damage induced by invading T cells in organotypic central nervous system tissue in vitro: involvement of microglial cells.

机译:在体外器官型中枢神经系统组织中入侵T细胞诱导的轴突损伤:小胶质细胞的参与。

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Neuroinflammation in the course of multiple sclerosis and experimental autoimmune encephalomyelitis results in demyelination and, recently demonstrated, axonal loss. Invading neuroantigen specific T cells are the crucial cellular elements in these processes. Here we demonstrate that invasion of activated T cells induces a massive microglial attack on myelinated axons in entorhinal-hippocampal slice cultures. Flow cytometry analysis of activation markers revealed that the activation state of invading MBP-specific T cells was significantly lower in comparison to PMA-activated T cells. Moreover, MBP-specific T cells showed a significantly lower secretion of IFN-gamma. Conversely, MBP-specific T cells displayed a significantly higher potential to trigger activation of microglial cells, i.e. upregulation of MHC class II and ICAM-1 expression, and, most importantly, microglial phagocytosis of pre-traced axons. Our data suggest that this was mediated via specific cellular interactions of T cells and microglial cells since IFN-gamma alone was not sufficient to induce axonal damage while such damage was apparent in response to TNF-alpha which is released by activated microglial cells. TNF-alpha secretion by both T cell populations was negligible. Thus, MBP-specific T cells which invade nervous tissue in the course of neuroinflammation are more effective in axon-damaging recruiting microglial cells than activated T cells of other specificities.
机译:在多发性硬化和实验性自身免疫性脑脊髓炎的过程中,神经炎症会导致脱髓鞘,并且最近证明是轴突丢失。侵袭性神经抗原特异性T细胞是这些过程中至关重要的细胞成分。在这里,我们证明了激活的T细胞的入侵在Ennerhinal-海马切片培养物中诱导对髓鞘轴突的大规模小胶质细胞攻击。激活标记的流式细胞仪分析表明,与PMA激活的T细胞相比,入侵的MBP特异性T细胞的激活状态明显更低。此外,MBP特异性T细胞显示出明显较低的IFN-γ分泌。相反,MBP特异性T细胞显示出显着更高的潜力来触发小胶质细胞的活化,即,MHC II类和ICAM-1表达的上调,最重要的是,预先追踪的轴突的小胶质细胞吞噬作用。我们的数据表明,这是通过T细胞和小胶质细胞的特异性细胞相互作用介导的,因为仅IFN-γ不足以诱导轴突损伤,而这种损伤是对活化小胶质细胞释放的TNF-α的反应明显的。两个T细胞群的TNF-α分泌微不足道。因此,在神经炎症过程中侵入神经组织的MBP特异性T细胞比其他活化的T细胞在轴突损伤募集的小胶质细胞中更有效。

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