Roh M S, Wang L, Oyedeji C, LeRoux M E, Curley S A, Pollock R E, Klostergaard J
Department of General Surgery, University of Texas MD Anderson Cancer Center, Houston 77030.
Surgery. 1990 Aug;108(2):400-4; discussion 404-5. doi: 10.1002/bjs.1800770937.
Colorectal liver metastases are a common clinical problem and require more effective therapy. Kupffer cells (KC) perform many important homeostatic functions within the liver and may also possess the ability to mediate tumor cytotoxicity. We investigated the ability of human KC to mediate cytotoxicity against human colon adenocarcinoma targets (HT 29) in vitro. Unstimulated human KC were cytotoxic against the HT 29 targets at all effector/target ratios tested. This cytotoxicity was increased significantly (p less than 0.05) when the KC were stimulated with interferon-gamma and lipopolysaccharide. Human KC produced tumor necrosis factor (TNF), and KC stimulation significantly (p less than 0.05) increased secretion of this monokine. The addition of anti-TNF antibody to the KC-HT 29 cocultures completely neutralized all of the available TNF yet cytotoxicity was not affected, suggesting the participation of a membrane-bound form of TNF or other mechanisms.
结直肠癌肝转移是一个常见的临床问题,需要更有效的治疗方法。库普弗细胞(KC)在肝脏内执行许多重要的稳态功能,并且可能还具有介导肿瘤细胞毒性的能力。我们研究了人KC在体外介导针对人结肠腺癌靶细胞(HT 29)的细胞毒性的能力。在所有测试的效应细胞/靶细胞比例下,未受刺激的人KC对HT 29靶细胞具有细胞毒性。当KC用干扰素-γ和脂多糖刺激时,这种细胞毒性显著增加(p小于0.05)。人KC产生肿瘤坏死因子(TNF),并且KC刺激显著(p小于0.05)增加了这种单核因子的分泌。向KC-HT 29共培养物中添加抗TNF抗体完全中和了所有可用的TNF,但细胞毒性并未受到影响,这表明存在膜结合形式的TNF或其他机制参与其中。