Lampson L A
Department of Neurology, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Microsc Res Tech. 1995 Nov 1;32(4):267-85. doi: 10.1002/jemt.1070320402.
MHC-restricted T cells are thought to contribute to clinical demyelination in MS and other circumstances. The step-by-step mechanisms involved and ways of controlling them are still being defined. Identification of the MHC+ cells in the CNS in situ has been controversial. This chapter reviews MHC expression in neural tissue, including normal, pathological, experimental, and developing tissue in situ and isolated cells in vitro. A basic pattern is defined, in which MHC expression is limited to nonneural cells and strongest class I and II expression are on different cell types. Variations from the basic pattern are reviewed. Ways of reconciling divergent findings are discussed, including the use of "mock tissue" to help choose between technical and biological bases for divergent findings, the potential contribution of internal antigen to the in situ staining patterns, and the possibility that class I upregulation is actively suppressed in situ. Functional implications of the observed patterns of MHC expression and ways of confirming the function of each MHC+ cell type in situ are described. It is suggested that modulating MHC expression in different cell types at different times or in different directions might be desirable.
MHC 限制性 T 细胞被认为在多发性硬化症及其他情况下导致临床脱髓鞘。其中涉及的逐步机制以及控制这些机制的方法仍在确定之中。在中枢神经系统原位鉴定 MHC+细胞一直存在争议。本章回顾了神经组织中的 MHC 表达,包括正常、病理、实验和发育中的原位组织以及体外分离的细胞。定义了一种基本模式,其中 MHC 表达限于非神经细胞,且最强的 I 类和 II 类表达存在于不同细胞类型上。回顾了与基本模式的差异。讨论了调和不同研究结果的方法,包括使用“模拟组织”来帮助在不同研究结果的技术和生物学基础之间做出选择、内源性抗原对原位染色模式的潜在贡献,以及 I 类上调在原位被积极抑制的可能性。描述了观察到的 MHC 表达模式的功能意义以及原位确认每种 MHC+细胞类型功能的方法。有人提出,在不同时间或不同方向调节不同细胞类型中的 MHC 表达可能是可取的。