人粒细胞产生肿瘤坏死因子。

Y Mándi, V Endrész, L Krenács, K Régely, M Degré, I Béládi
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引用次数: 17

摘要

人多形核白细胞在18小时51Cr释放试验中杀死WEHI 164细胞。人肿瘤坏死因子(TNF)抗体阻断人粒细胞介导的靶细胞裂解。静止的粒细胞产生不可检测的TNF,如果有的话。金黄色葡萄球菌刺激的粒细胞释放250-500 U/ml TNF α。通过中和抗TNF α单克隆抗体,在WEHI 164细胞毒性试验中证实了释放的TNF的特异性。内皮细胞对胸腺嘧啶的摄取被粒细胞来源的TNF抑制。通过Sephacryl S-200凝胶过滤,分子量测定进一步证实了TNF α的身份,结果约为44,000。因此,粒细胞除了具有抗菌能力外,还可能通过释放TNF参与肿瘤排斥反应、炎症和脓毒性感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor necrosis factor production by human granulocytes.

Human polymorphonuclear leukocytes kill WEHI 164 cells in an 18-hour 51Cr release assay. Antibody to human tumor necrosis factor (TNF) blocks the lysis of targets mediated by human granulocytes. Resting granulocytes produce an undetectable amount of TNF, if any. Granulocytes stimulated with Staphylococcus aureus release 250-500 U/ml TNF alpha. The specificity of the released TNF in the WEHI 164 cytotoxicity assay was confirmed by using neutralizing anti-TNF alpha monoclonal antibodies. The thymidine uptake of endothelial cells was inhibited by granulocyte-derived TNF. The identity of TNF alpha was further confirmed by molecular weight determination, by gel filtration on Sephacryl S-200, with a result of approximately 44,000. Besides their antimicrobial capacity, therefore, granulocytes may contribute to tumor rejection, inflammation and septic infections by releasing TNF.

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