首页> 外文期刊>Scandinavian journal of immunology. >NKG2D ligands expression and NKG2D-mediated cytotoxicity in human laryngeal squamous carcinoma cells.
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NKG2D ligands expression and NKG2D-mediated cytotoxicity in human laryngeal squamous carcinoma cells.

机译:NKG2D配体表达和NKG2D介导的人喉鳞状细胞癌细胞毒性。

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摘要

The NKG2D is an activating immunoreceptor expressed by NK cells and CD8(+) T cells. Engagement of NKG2D by its ligands is critical for both innate and adoptive immunity. While the overexpression of NKG2D ligands on certain tumour cells has previously been demonstrated, little is known about NKG2D ligand expression on human laryngeal tumour cells. In this study, we first verified that the interaction between NKG2D and its ligands was critical for NK cell-based immune response to human laryngeal squamous carcinoma cells Hep-2. This NKG2D-mediated effect was observed by transfecting the recombinant eukaryotic expression vector pEGFP-N1/NKG2D as well as the NKG2D blockade. The mRNA and protein expression of NKG2D ligands, MHC class I-related chain molecules A (MICA) and UL16-binding proteins (ULBPs), in human laryngeal carcinoma cell line Hep-2 and fresh tumour tissues were evaluated. Compared with non-tumour tissues of vocal cords polyps, MICA and ULBP-3 were strongly overexpressed on both the human laryngeal carcinoma cell line Hep-2 and fresh human laryngeal carcinoma tissues. The mechanism and impact of NKG2D ligands overexpression on NK cell-mediated anti-laryngeal cancer immune response would require further investigation.
机译:NKG2D是由NK细胞和CD8(+)T细胞表达的一种活化免疫受体。 NKG2D与其配体的结合对于先天免疫和过继免疫均至关重要。尽管先前已经证明了NKG2D配体在某些肿瘤细胞上的过表达,但对NKG2D配体在人喉肿瘤细胞上的表达知之甚少。在这项研究中,我们首先验证了NKG2D及其配体之间的相互作用对于基于NK细胞对人喉鳞状细胞癌Hep-2的免疫反应至关重要。通过转染重组真核表达载体pEGFP-N1 / NKG2D以及NKG2D阻滞,可以观察到这种NKG2D介导的作用。评估了人喉癌细胞系Hep-2和新鲜肿瘤组织中NKG2D配体,MHC I类相关链分子A(MICA)和UL16结合蛋白(ULBPs)的mRNA和蛋白表达。与声带息肉的非肿瘤组织相比,MICA和ULBP-3在人喉癌细胞系Hep-2和新鲜的人喉癌组织中均强烈过表达。 NKG2D配体过表达对NK细胞介导的抗喉癌免疫应答的机制及其影响尚需进一步研究。

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