Strachan-Whaley Megan, Rivest Serge, Yong V Wee
1 Hotchkiss Brain Institute and Department of Clinical Neurosciences, University of Calgary , Alberta, Canada .
J Interferon Cytokine Res. 2014 Aug;34(8):615-22. doi: 10.1089/jir.2014.0019.
Brain-resident microglia and T lymphocytes recruited into the central nervous system both play important roles in the neuropathology of multiple sclerosis. The microglia and recruited T cells are in close proximity in lesions of multiple sclerosis and in animal models, suggesting their potential for interactions. In support, microglia and T cells express a number of molecules that permit their engagement. Here we describe the interactions between T cells and microglia and the myriad responses that can result. These interactions include antigen presentation by microglia to activate T cells, the T cell activation of microglia, their progressive stimulation of one another, and the production of injurious or neurotrophic outcomes in their vicinity. Important considerations for the future include the nature of the T helper cell subsets and the M1 and M2 polarized nature of microglia, as the interactions between different subsets likely result in particular functions and outcomes. That T cells and microglia are in proximity and that they interact in lesions in the central nervous system implicate them as modifiers of pathobiology in multiple sclerosis.
驻留在脑内的小胶质细胞和招募到中枢神经系统的T淋巴细胞在多发性硬化症的神经病理学中均发挥重要作用。在多发性硬化症的病变部位以及动物模型中,小胶质细胞和招募来的T细胞紧密相邻,这表明它们具有相互作用的可能性。作为佐证,小胶质细胞和T细胞表达多种能够使它们相互作用的分子。在此,我们描述T细胞与小胶质细胞之间的相互作用以及可能产生的众多反应。这些相互作用包括小胶质细胞呈递抗原来激活T细胞、T细胞激活小胶质细胞、它们彼此之间的逐步刺激以及在其附近产生有害或神经营养性结果。未来需要重点考虑的因素包括辅助性T细胞亚群的性质以及小胶质细胞的M1和M2极化性质,因为不同亚群之间的相互作用可能会导致特定的功能和结果。T细胞和小胶质细胞在中枢神经系统病变部位相邻且相互作用,这表明它们是多发性硬化症病理生物学的调节因子。