Aono K, Isobe K, Nakashima I, Kondo S, Miyachi M, Nimura Y
First Department of Surgery, Nagoya University, School of Medicine, Japan.
Biochem Biophys Res Commun. 1994 Jun 30;201(3):1175-81. doi: 10.1006/bbrc.1994.1829.
We have previously demonstrated that rat resting macrophages have cytotoxicity against tumor cells. In the current study we have performed an in vitro experiment to explore the mechanism of Kupffer cells-mediated cytotoxicity against hepatomas. The coculture of tumor cells with Kupffer cells (derived from rat livers) stimulated syngeneic and allogeneic Kupffer cells to produce nitric oxide. Kupffer cell-mediated cytotoxicity was paralleled to the amount of nitric oxide and was abolished by the addition of NG-monomethyl-L-arginine. The ability to stimulate Kupffer cells to produce nitric oxide resided on the membranous fragment of tumor cells.
我们之前已经证明,大鼠静止巨噬细胞对肿瘤细胞具有细胞毒性。在当前研究中,我们进行了一项体外实验,以探究库普弗细胞介导的对肝癌细胞毒性作用的机制。肿瘤细胞与(源自大鼠肝脏的)库普弗细胞共培养可刺激同基因和异基因库普弗细胞产生一氧化氮。库普弗细胞介导的细胞毒性与一氧化氮的量平行,并且通过添加NG-单甲基-L-精氨酸可消除这种毒性。刺激库普弗细胞产生一氧化氮的能力存在于肿瘤细胞的膜片段上。