Suppr超能文献

肿瘤坏死因子可增强人类肿瘤细胞中HLA - A、B、C和HLA - DR基因的表达。

Tumor necrosis factor enhances HLA-A,B,C and HLA-DR gene expression in human tumor cells.

作者信息

Pfizenmaier K, Scheurich P, Schlüter C, Krönke M

出版信息

J Immunol. 1987 Feb 1;138(3):975-80.

PMID:2433337
Abstract

Tumor necrosis factor-alpha (TNF-alpha) exerts multiple biologic activities, which include such diverse effects as direct tumoricidal activity and stimulation of metabolic activities as well as expression of cell surface antigens on nonmalignant cells. We report here that in various human tumor cells TNF-alpha upregulates constitutively expressed HLA genes. Further, in a priori HLA-negative tumor cells, TNF-alpha enhances IFN-gamma-induced class I and class II HLA gene expression. In vitro transcription, Northern blot, and immunofluorescence analysis performed with the leukemic cell line K 562 reveal that TNF-alpha reversibly enhances IFN-gamma-induced HLA gene expression at the level of mRNA transcription. In addition, a posttranscriptional regulation of HLA gene expression by TNF-alpha is suggested from enhancement of HLA class I membrane expression in Colo 205 cells without measurable changes in steady state mRNA levels. Therefore, it is conceivable that TNF-alpha, similar to IFN-gamma, might provoke tumor rejection not only via direct tumoricidal action but also via enhancement of HLA antigens and induction of tumor-specific immune responses.

摘要

肿瘤坏死因子-α(TNF-α)具有多种生物学活性,包括直接杀肿瘤活性、刺激代谢活性以及非恶性细胞上细胞表面抗原的表达等多种不同作用。我们在此报告,在各种人类肿瘤细胞中,TNF-α上调组成性表达的HLA基因。此外,在预先HLA阴性的肿瘤细胞中,TNF-α增强干扰素-γ诱导的I类和II类HLA基因表达。用白血病细胞系K 562进行的体外转录、Northern印迹和免疫荧光分析表明,TNF-α在mRNA转录水平可逆地增强干扰素-γ诱导的HLA基因表达。此外,在Colo 205细胞中,TNF-α增强HLA I类膜表达,但稳态mRNA水平无明显变化,提示TNF-α对HLA基因表达有转录后调控作用。因此,可以想象,TNF-α与干扰素-γ类似,可能不仅通过直接杀肿瘤作用,还通过增强HLA抗原和诱导肿瘤特异性免疫反应来引发肿瘤排斥。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验