通过回收表面HLA-DR分子来介导抗原呈现
V Pinet1, M Vergelli, R Martin
1Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Nature
|June 15, 1995
概括
表面的HLA-DR分子通过细胞质尾巴回收,使某些抗原的呈现成为可能. 这揭示了一种替代的抗原呈现途径,与传统的不变链依赖路径不同.
科学领域:
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 第二类基因相容性分子从内细胞区向T细胞呈现.
- 抗原呈现通常涉及新合成的II类分子,不变链和HLA-DM.
- 常规抗原呈现规则的例外机制尚不清楚.
研究的目的:
- 调查替代抗原呈现途径背后的机制.
- 确定HLA-DR分子回收在抗原呈现中的作用.
- 阐明HLA-DR细胞质尾巴在抗原呈现中的功能.
主要方法:
- 研究了流感血氨酸和髓基本蛋白质表征的呈现.
- 截断的HLA-DR分子的α或β细胞质尾巴.
- 评估了HLA-DR分子的内部化和抗原呈现.
- 血凝素和矩阵抗原的比较表现.
主要成果:
- 与表面HLA-DR分子回收相关的特定表位的呈现.
- 切断HLA-DR细胞质尾巴取消了HLA-DR内部化和相关的抗原呈现.
- 不变的链依赖抗原呈现不受这些切断的影响.
- 细胞质尾巴的HLA-DR对另一个取决于内化的途径至关重要.
结论:
- HLA-DR细胞质尾巴介导一种涉及分子内部化的替代抗原呈现途径.
- 这种路径与传统的不变链依赖路径不同.
- 表面HLA-DR分子的回收对于呈现特定的免疫主导表位是必不可少的.
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