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引用本文的文献

1
The multifaceted profile of activated microglia.活化小胶质细胞的多方面特征。
Mol Neurobiol. 2009 Oct;40(2):139-56. doi: 10.1007/s12035-009-8077-9. Epub 2009 Jul 23.

长期脱髓鞘后中枢神经系统中MHC II的表达。

MHC II expression in the CNS after long-term demyelination.

作者信息

Cannella B, Aquino D A, Raine C S

机构信息

Department of Pathology (Neuropathology), Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

J Neuropathol Exp Neurol. 1995 Jul;54(4):521-30. doi: 10.1097/00005072-199507000-00006.

DOI:10.1097/00005072-199507000-00006
PMID:7602325
Abstract

The ability of chronically demyelinated central nervous system (CNS) tissue to express major histocompatibility complex (MHC) class II molecules has been measured in mouse spinal cord cultures exposed for 1 and 3 weeks to demyelinating anti-white matter (WM) serum. From previous studies, it was known that after 3 weeks of demyelination in vitro, such cultures are incapable of remyelination. In the present report, MHC II levels were evaluated by immunocytochemistry and by Western and Northern blots. The results have shown that after both 1 and 3 weeks of exposure to myelinotoxic anti-WM serum, the cultures retained the ability to express MHC II and this could be further upregulated by incubation with interferon gamma (IFN gamma). Control groups showed increased expression of MHC II with age. By immunocytochemistry, all groups of cultures expressed high levels of MHC II and all groups showed upregulation after IFN gamma treatment. Anti-WM-treated cultures demonstrated slightly higher levels of MHC II than controls. Morphologically, the MHC II expression was associated with the surface of astrocytes. Semiquantitative analysis by Western blotting confirmed the increase in class II MHC expression in the long-term treated cultures after IFN gamma exposure, revealing no differences between anti-WM-treated and complement-treated cultures. This was also supported by Northern blotting which showed similar mRNA levels in both groups. These findings suggest that long-term demyelinated CNS tissue still possesses the ability to interact with CD4+ T cells, observations of significance to the expansion of the chronic multiple sclerosis lesion.

摘要

在暴露于脱髓鞘抗白质(WM)血清1周和3周的小鼠脊髓培养物中,已检测了慢性脱髓鞘中枢神经系统(CNS)组织表达主要组织相容性复合体(MHC)II类分子的能力。从先前的研究可知,体外脱髓鞘3周后,此类培养物无法进行髓鞘再生。在本报告中,通过免疫细胞化学、蛋白质免疫印迹法和RNA印迹法评估了MHC II水平。结果显示,在暴露于髓鞘毒性抗WM血清1周和3周后,培养物均保留了表达MHC II的能力,并且通过与γ干扰素(IFNγ)孵育可进一步上调其表达。对照组显示MHC II表达随年龄增加。通过免疫细胞化学,所有培养物组均表达高水平的MHC II,并且所有组在IFNγ处理后均出现上调。抗WM处理的培养物显示MHC II水平略高于对照组。形态学上,MHC II表达与星形胶质细胞表面相关。蛋白质免疫印迹法的半定量分析证实,IFNγ暴露后长期处理的培养物中II类MHC表达增加,显示抗WM处理的培养物与补体处理的培养物之间无差异。RNA印迹法也支持了这一点,其显示两组中的mRNA水平相似。这些发现表明,长期脱髓鞘的CNS组织仍具有与CD4 + T细胞相互作用的能力,这一观察结果对慢性多发性硬化症病变的扩展具有重要意义。