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I类主要组织相容性复合体转基因小鼠中的髓鞘形成异常

Dysmyelination in class I MHC transgenic mice.

作者信息

Turnley A M, Morahan G

机构信息

Walter and Eliza Hall Institute of Medical Research, P.O. Royal Melbourne Hospital, Parkville, Victoria, Australia.

出版信息

Microsc Res Tech. 1995 Nov 1;32(4):286-94. doi: 10.1002/jemt.1070320403.

Abstract

Why is it that oligodendrocytes do not normally express major histocompatibility complex (MHC) molecules? To examine the effect of aberrant MHC expression in oligodendrocytes, transgenic mice have been produced which expressed the class I MHC gene, H-2Kb, under direction of the MBP promoter [Turnley et al. (1991b) Nature, 353:566-569; Yoshioka et al. (1991) Mol. Cell. Biol., 11:5479-5486]. A proportion of these mice exhibited a shivering phenotype, with tonic seizures and early death. Oligodendrocyte function and viability was shown to be affected, resulting in severe dysmyelination of the CNS. Is this phenomenon of cell damage due to aberrant expression of MHC molecules restricted to oligodendrocytes, and could other, non-MHC molecules, when aberrantly expressed, result in similar cell damage? This paper discusses these questions and examines possible mechanisms for the oligodendrocyte damage and hypomyelination observed in these transgenic mice. Finally, the implications of aberrant MHC expression in oligodendrocytes for demyelinating diseases such as multiple sclerosis are discussed.

摘要

为什么少突胶质细胞通常不表达主要组织相容性复合体(MHC)分子?为了研究少突胶质细胞中异常MHC表达的影响,已培育出在髓鞘碱性蛋白(MBP)启动子的调控下表达I类MHC基因H-2Kb的转基因小鼠[特恩利等人(1991年b)《自然》,353:566 - 569;吉冈等人(1991年)《分子与细胞生物学》,11:5479 - 5486]。这些小鼠中有一部分表现出颤抖的表型,伴有强直性惊厥和早期死亡。已证明少突胶质细胞的功能和活力受到影响,导致中枢神经系统严重脱髓鞘。这种由于MHC分子异常表达导致的细胞损伤现象是否仅限于少突胶质细胞,以及其他非MHC分子异常表达时是否会导致类似的细胞损伤?本文讨论了这些问题,并研究了在这些转基因小鼠中观察到的少突胶质细胞损伤和髓鞘形成不足的可能机制。最后,讨论了少突胶质细胞中异常MHC表达对诸如多发性硬化症等脱髓鞘疾病的影响。

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