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在体内,当树突状细胞与靶细胞被CD8(+) T细胞识别时,通过噬细胞作用摄取膜成分的过程就会发生。

Capture of membrane components via trogocytosis occurs in vivo during both dendritic cells and target cells encounter by CD8(+) T cells.

作者信息

Riond J, Elhmouzi J, Hudrisier D, Gairin J E

机构信息

CRPS, UMR2587 CNRS, Pierre Fabre, Toulouse, France.

出版信息

Scand J Immunol. 2007 Oct;66(4):441-50. doi: 10.1111/j.1365-3083.2007.01996.x.

DOI:10.1111/j.1365-3083.2007.01996.x
PMID:17850589
Abstract

Cytotoxic T lymphocytes recently stimulated by antigen-presenting cells (APC) display major histocompatibility class (MHC) I and II molecules inherited from APC. We have previously reported that, in vitro, transfer of MHC molecules and several other proteins occurs through trogocytosis, i.e. the active acquisition of target cell membrane fragments by T lymphocytes. Here, using the model of viral antigen LCMVgp33-41 recognition in transgenic P14 mice, we show that CD8(+) T cells perform trogocytosis in vivo, as detected by the capture of biotin- or fluorescence-labeled components of the APC surface. Trogocytosis occurs during interactions of CD8(+) T cells with at least two kinds of cells: target cells and dendritic cells (DC). In lymph nodes, CD8(+) T cells having performed trogocytosis with DC express the CD69 activation marker indicating that trogocytosis detects recently activated cells. Taken together, our findings suggest that trogocytosis may be a new in vivo marker of the recent interaction between a CD8(+) T cell and its cellular partners or targets.

摘要

最近被抗原呈递细胞(APC)激活的细胞毒性T淋巴细胞会展示从APC继承而来的主要组织相容性复合体(MHC)I类和II类分子。我们之前报道过,在体外,MHC分子和其他几种蛋白质的转移是通过胞啃作用发生的,即T淋巴细胞主动摄取靶细胞膜片段。在这里,我们利用转基因P14小鼠中病毒抗原LCMVgp33 - 41识别模型,发现CD8(+) T细胞在体内会进行胞啃作用,这可通过捕获APC表面生物素或荧光标记成分来检测。胞啃作用发生在CD8(+) T细胞与至少两种细胞的相互作用过程中:靶细胞和树突状细胞(DC)。在淋巴结中,与DC发生胞啃作用的CD8(+) T细胞表达CD69激活标志物,这表明胞啃作用可检测到最近被激活的细胞。综上所述,我们的研究结果表明,胞啃作用可能是CD8(+) T细胞与其细胞伙伴或靶标之间近期相互作用的一种新的体内标志物。

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