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MHC II类分子和CD44分子参与肿瘤细胞刺激的人单核细胞诱导肿瘤坏死因子(TNF)基因表达的过程。

The MHC class-II and CD44 molecules are involved in the induction of tumour necrosis factor (TNF) gene expression by human monocytes stimulated with tumour cells.

作者信息

Zembala M, Siedlar M, Ruggiero I, Wieckiewicz J, Mytar B, Mattei M, Colizzi V

机构信息

Department of Clinical Immunology, Jagiellonian University Medical School, Cracow, Poland.

出版信息

Int J Cancer. 1994 Jan 15;56(2):269-74. doi: 10.1002/ijc.2910560221.

Abstract

Tumour necrosis factor alpha (TNF) mRNA is detected in the macrophage infiltrate surrounding the tumour, but the cellular/molecular interactions leading to TNF gene expression in macrophages are unknown. The in vitro system in which human blood monocytes are stimulated with human cancer cells for TNF release was used to study such interactions. Monoclonal antibodies (MAbs) against various adhesion molecules (LFA-1, LFA-3, ICAM-1, VNR, VLA beta I chain) were unable to block TNF production in co-culture of monocytes with a human pancreatic carcinoma (HPC) cell line. However, anti-CD44 and anti-HLA-DR MAbs effectively blocked TNF release and TNF-mRNA induction in monocytes. Pre-incubation of monocytes with anti-HLA-DR and tumour cells with anti-CD44 MAbs had a similar effect. It was concluded that CD44 molecules are involved in tumour-monocyte interactions and that HLA-DR determinants of monocytes are engaged in signal transduction for TNF gene activation. These findings may suggest that certain surface determinants of tumour cells act as ligands for MHC class-II molecules and induce TNF production in monocytes.

摘要

在肿瘤周围的巨噬细胞浸润中可检测到肿瘤坏死因子α(TNF)信使核糖核酸(mRNA),但导致巨噬细胞中TNF基因表达的细胞/分子相互作用尚不清楚。利用人血单核细胞与人癌细胞共培养以释放TNF的体外系统来研究此类相互作用。针对各种黏附分子(淋巴细胞功能相关抗原-1(LFA-1)、淋巴细胞功能相关抗原-3(LFA-3)、细胞间黏附分子-1(ICAM-1)、玻连蛋白受体(VNR)、极迟抗原βⅠ链(VLA β I链))的单克隆抗体(MAbs)无法阻断单核细胞与人类胰腺癌细胞系(HPC)共培养时TNF的产生。然而,抗CD44和抗人白细胞抗原-DR(HLA-DR)单克隆抗体可有效阻断单核细胞中TNF的释放及TNF-mRNA的诱导。用抗HLA-DR预处理单核细胞以及用抗CD44单克隆抗体预处理肿瘤细胞也有类似效果。得出的结论是,CD44分子参与肿瘤-单核细胞相互作用,单核细胞的HLA-DR决定簇参与TNF基因激活的信号转导。这些发现可能表明肿瘤细胞的某些表面决定簇充当MHCⅡ类分子的配体并诱导单核细胞产生TNF。

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