Suppr超能文献

一种用于检测人单核细胞细胞毒性因子/肿瘤坏死因子的高敏感性细胞系——WEHI 164克隆13。

A highly sensitive cell line, WEHI 164 clone 13, for measuring cytotoxic factor/tumor necrosis factor from human monocytes.

作者信息

Espevik T, Nissen-Meyer J

出版信息

J Immunol Methods. 1986 Dec 4;95(1):99-105. doi: 10.1016/0022-1759(86)90322-4.

Abstract

By limiting dilution of WEHI 164 mouse fibrosarcoma cells we have isolated a cell line, WEHI 164 clone 13, which is extremely sensitive to cytotoxic factor (CF) derived from human monocytes. By using WEHI 164 clone 13 in a MTT tetrazolium cytotoxicity assay it was found that CF supernatants from activated monocytes had to be diluted 10(5)-10(6) times to reach the dose which produced 50% dead cells (LD50). By comparing the LD50 of different target cells, WEHI 164 clone 13 cells were found to be approximately 10(3) times more sensitive for CF-induced cytotoxicity as compared to WEHI 164 parental cells and approximately 10(2) times more sensitive as compared to actinomycin D-treated L929 cells. Treatment of the WEHI 164 clone 13 cells with actinomycin D did not increase their sensitivity for CF-induced cytotoxicity. Recombinant tumor necrosis factor (rTNF) also mediated high cytotoxicity towards WEHI 164 clone 13 cells, with an LD50 of 2 X 10(-3) ng/ml. Neutralizing CF antiserum completely inhibited the toxic activity of rTNF. WEHI 164 clone 13 cells were highly sensitive to monocyte-mediated cytotoxicity in that 1-2 monocytes were able to kill at least 5000 of these target cells. Neutralizing TNF antiserum completely inhibited monocyte-mediated cytotoxicity. These results indicate that the high level of cytotoxicity mediated by CF supernatants and monocytes on WEHI 164 clone 13 cells is due to TNF as the effector molecule.

摘要

通过对WEHI 164小鼠纤维肉瘤细胞进行有限稀释,我们分离出了一个细胞系,即WEHI 164克隆13,它对源自人单核细胞的细胞毒性因子(CF)极为敏感。在MTT四唑盐细胞毒性试验中使用WEHI 164克隆13发现,活化单核细胞的CF上清液必须稀释10⁵ - 10⁶倍才能达到产生50%死亡细胞的剂量(LD50)。通过比较不同靶细胞的LD50,发现与WEHI 164亲代细胞相比,WEHI 164克隆13细胞对CF诱导的细胞毒性的敏感性大约高10³倍,与放线菌素D处理的L929细胞相比大约高10²倍。用放线菌素D处理WEHI 164克隆13细胞并没有增加它们对CF诱导的细胞毒性的敏感性。重组肿瘤坏死因子(rTNF)对WEHI 164克隆13细胞也介导了高细胞毒性,LD50为2×10⁻³ ng/ml。中和CF抗血清完全抑制了rTNF的毒性活性。WEHI 164克隆13细胞对单核细胞介导的细胞毒性高度敏感,1 - 2个单核细胞就能杀死至少5000个这些靶细胞。中和TNF抗血清完全抑制了单核细胞介导的细胞毒性。这些结果表明,CF上清液和单核细胞对WEHI 164克隆13细胞介导的高水平细胞毒性是由于TNF作为效应分子所致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验