Monastra G, Cabrelle A, Zambon A, Rosato A, Macino B, Collavo D, Zanovello P
Institute of Oncology, Inter-University Center for Cancer Research, University of Padova, Italy.
Cell Immunol. 1996 Jul 10;171(1):102-10. doi: 10.1006/cimm.1996.0179.
Tumor necrosis factor alpha, in the secreted as well as membrane-associated (mTNF alpha) form, represents a cytotoxic effector mechanism of activated macrophages; in contrast, direct evidence of the mTNF alpha involvement in cytotoxic T lymphocyte (CTL)-mediated lysis has not yet been obtained. We observed that following activation with anti-CD3 monoclonal antibody (mAb), both cloned CTL and peritoneal exudate lymphocytes rapidly upregulated mTNF alpha; a similar effect was observed in the macrophage cell line J774 after stimulation with lipopolysaccharide endotoxin. Activated effector cells, which were fixed with paraformaldehyde before testing, exerted lytic activity against the TNF-sensitive WEHI 164 tumor cell line, but not against the TNF-resistant P-815 mastocytoma. This effect was completely inhibited in the presence of anti-mouse TNF alpha Ab. Moreover, both mTNF alpha-expressing macrophages and CTL induced nuclear DNA fragmentation in WEHI 164 cells, which was also blocked by anti-TNF alpha Ab and was accompanied by a morphologic degeneration characteristic of the apoptotic form of cell death. These data on the whole indicate a common mode of action for mTNF alpha expressed on different cell populations endowed with cytotoxic capability and also imply a role for this molecule in T-cell-mediated cytotoxicity.
肿瘤坏死因子α,以分泌形式以及膜相关形式(mTNFα)存在,代表活化巨噬细胞的一种细胞毒性效应机制;相比之下,尚未获得mTNFα参与细胞毒性T淋巴细胞(CTL)介导的细胞裂解的直接证据。我们观察到,在用抗CD3单克隆抗体(mAb)激活后,克隆的CTL和腹腔渗出淋巴细胞均迅速上调mTNFα;在用脂多糖内毒素刺激后,巨噬细胞系J774中也观察到类似的效应。在测试前用多聚甲醛固定的活化效应细胞,对TNF敏感的WEHI 164肿瘤细胞系具有裂解活性,但对TNF抗性的P - 815肥大细胞瘤则没有。在抗小鼠TNFα抗体存在的情况下,这种效应被完全抑制。此外,表达mTNFα的巨噬细胞和CTL均诱导WEHI 164细胞中的核DNA片段化,这也被抗TNFα抗体阻断,并伴有细胞凋亡形式的形态学退化特征。总体而言,这些数据表明在具有细胞毒性能力的不同细胞群体上表达的mTNFα具有共同的作用模式,也暗示该分子在T细胞介导的细胞毒性中发挥作用。