抗原处理突变细胞中的HLA-A2分子含有来自信号序列的
1Department of Microbiology and Immunology, Duke University Medical Center, Durham, North Carolina 27710.
Nature
|April 2, 1992
概括
突变的T2细胞显示出缺陷的抗原呈现,这是由于类运输到内 плазма网膜 (ER) 的问题. 令人惊的是,在T2细胞中表达的小鼠I类分子缺乏,表明缺乏.
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:
- 突变的T2细胞通过人类I类 (HLA) 分子表现出抗原的缺陷.
- 这些缺陷与抗原的输送到内细胞网膜 (ER) 的损害有关.
- 第I类主要基因相容性复合体 (MHC) 分子需要结合以获得稳定性和表面表达.
研究的目的:
- 研究T2细胞中小鼠 (H-2) 和人类 (HLA) I类分子的结能力.
- 为了确定"空"的I类分子是否不稳定或保留在ER中.
- 为了识别T2细胞中与HLA-A2分子结合的内源性.
主要方法:
- 在T2细胞中表达小鼠H-2和人类HLA-A2.
- 对I类分子的表面表达和结合的分析.
- 结合的序列. 结合的序列.
主要成果:
- 在T2细胞中表面表达的HLA-A2和H-2分子在很大程度上缺乏.
- "空"的H-2分子是稳定的,并在细胞表面表达.
- HLA-A2分子与有限的一组内源性结合,包括异常长度.
- 从IP-30的信号序列和未知来源获得的鉴定.
结论:
- "空"小鼠I类分子是稳定的,不会留在急诊室.
- HLA-A2分子结合特定的内源性,包括信号片段.
- 在ER运输之前,HLA-A2的基生成可能发生在细胞质中.
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