Besides their "classical" antigenic peptide-presenting activity, major histocompatibility complex (MHC) class II antigens can activate different cellular functions in immune and nonimmune cells. However, this "nonclassical" role and its functional consequences are still substantially overlooked. In
Expression of major histocompatibility complex class I antigens in the demyelinating twitcher CNS and PNS
β Scribed by Masako Taniike; Jill R. Marcus; Brian Popko; Kinuko Suzuki
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 247 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0360-4012
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β¦ Synopsis
The expression of the major histocompatibility complex Class I antigens (Class I) was investigated in the nervous system of twitcher (C57BL/6J-twi), a murine model of Krabbe disease in humans. Class I mRNA expression was low in wild type and in twitcher mice prior to the onset of demyelination. However, immunoreactivity for Class I antigens was demonstrated in the spindle-shaped cells in the sciatic nerve and in ramified microglia, endothelial cells and Bergmann glia. In twitcher, transcription of Class I mRNA increased significantly with the progression of demyelination and Mac-1 1 macrophages/microglia express Class I immunoreactivity. Class I immunoreactivity was also found in CD3 1 T-cells that were scattered in demyelinating lesions. CD8 1 or CD4 1 cells were also found in the demyelinating area. The results of this study indicate that immunoreactivity to Class I antigens is detected in certain cells even in the wild-type mice and that Class I expression is enhanced in the twitcher nervous system paralleling the progression of demyelination. Expression of MHC molecules in nonimmunological demyelinating disease such as twitcher may suggest a role of Class I molecules in the progression of demyelination. Alternatively, the expression may be a non-specific cellular response to the breakdown of myelin.
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