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HLA-DM在细胞表面表达,并与人朗格汉斯细胞中的HLA-DR和恒定链共定位。

HLA-DM is expressed on the cell surface and colocalizes with HLA-DR and invariant chain in human Langerhans cells.

作者信息

Andersson T, Patwardhan A, Emilson A, Carlsson K, Scheynius A

机构信息

Department of Biomedical Physics, Royal Institute of Technology, Stockholm, Sweden.

出版信息

Arch Dermatol Res. 1998 Dec;290(12):674-80. doi: 10.1007/s004030050372.

Abstract

The subcellular distribution patterns of molecules involved in the process of antigen loading [HLA-DR, HLA-DM, and the cytoplasmic and luminal parts of the invariant chain (Ii, CD74)] were investigated in Langerhans cells (LC), both qualitatively and quantitatively. The analysis was performed by immunofluorescence labelling of acetone-fixed vertical cryostat sections from normal human skin specimens and subsequent examination using confocal laser scanning microscopy (CSLM). The intensity-modulated multiple-wavelength scanning (IMS) technique was used to enhance channel separation when scanning dual-labelled specimens. The mean (n = 9) relative epidermal volumes of reactivity were: HLA-DR 8%+/-3%, HLA-DM 6%+/-2%, luminal Ii 6%+/-2%, and cytoplasmic Ii 4%+/-1%. The difference between HLA-DR and the other epitopes was significant at the P<0.001 level. All molecule combinations, except the combination of HLA-DM and luminal Ii (which was not studied), were to various extents colocalized. Experiments performed on unfixed epidermal sheets showed that HLA-DM is present on the cell surface of LC, suggesting that HLA-DM may interact with HLA-DR on the surface to induce peptide loading.

摘要

我们对参与抗原加载过程的分子[HLA-DR、HLA-DM以及恒定链(Ii,CD74)的胞质和腔部分]在朗格汉斯细胞(LC)中的亚细胞分布模式进行了定性和定量研究。分析通过对正常人皮肤标本的丙酮固定垂直冰冻切片进行免疫荧光标记,并随后使用共聚焦激光扫描显微镜(CSLM)进行检查来进行。在扫描双标记标本时,使用强度调制多波长扫描(IMS)技术来增强通道分离。平均(n = 9)相对表皮反应体积为:HLA-DR 8%±3%,HLA-DM 6%±2%,腔Ii 6%±2%,胞质Ii 4%±1%。HLA-DR与其他表位之间的差异在P<0.001水平上具有显著性。除了HLA-DM和腔Ii的组合(未进行研究)外,所有分子组合在不同程度上都有共定位。对未固定的表皮片进行的实验表明,HLA-DM存在于LC的细胞表面,这表明HLA-DM可能在表面与HLA-DR相互作用以诱导肽加载。

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