氯化锰增强小鼠细胞介导的细胞毒性:对自然杀伤细胞的影响。

R J Smialowicz, R R Rogers, M M Riddle, R W Luebke, D G Rowe, R J Garner
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引用次数: 19

摘要

在体外4小时51Cr释放实验中,单次注射氯化锰(MnCl2)可显著增强小鼠自然杀伤细胞(NK)活性。注射后活性增强持续数天。这种细胞毒活性与非粘附性脾细胞有关,并通过给mncl2处理的小鼠注射抗亚洲雪草GM1血清完全消除。在几种具有不同NK细胞反应性的小鼠品系(CBA/J、C57BL/6、A/J、C3H/HeJ和C57BL/6米色小鼠)和几种对NK细胞溶解具有不同敏感性的肿瘤靶细胞(YAC-1、RBL-5、EL-4和P815)中观察到锰增强的天然细胞毒性。在肿瘤攻击前一天注射MnCl2的小鼠,B16-F10黑色素瘤的生长受到抑制。氯化锰对NK细胞活性的增强似乎是由干扰素介导的。早在MnCl2注射后4小时,小鼠血清中就检测到低水平的IFN。兔抗小鼠IFN α、β而非抗小鼠IFN γ完全消除了mncl2增强的小鼠脾脏NK细胞活性。观察到的MnCl2对NK细胞活性的增强与报道的通过诱导IFN产生的更复杂的分子相似。
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Manganese chloride enhances murine cell-mediated cytotoxicity: effects on natural killer cells.

Natural killer (NK) cell activity of mice given a single injection of manganese chloride (MnCl2) was significantly enhanced as measured in a 4-hr in vitro 51Cr release assay. Enhanced activity persisted for several days after injection. This cytotoxic activity was associated with nonadherent spleen cells and was completely eliminated by injecting MnCl2-treated mice with anti-asialo GM1 serum. Manganese-enhanced natural cytotoxicity was observed in several mouse strains with differing NK cell reactivity (CBA/J, C57BL/6, A/J, C3H/HeJ, and C57BL/6 beige mice) and with several tumor target cells with differing sensitivity to NK cytolysis (YAC-1, RBL-5, EL-4, and P815). The growth of B16-F10 melanoma lung tumors was inhibited in mice injected with MnCl2 one day before tumor challenge. Manganese chloride enhancement of NK cell activity appeared to be mediated by interferon (IFN). Low levels of IFN were detected in the serum of mice as early as 4 hr after MnCl2 injection. Rabbit anti-mouse IFN alpha, beta but not anti-mouse IFN gamma completely eliminated the MnCl2-enhanced NK cell activity in the spleens of mice. The observed enhancement of NK cell activity by MnCl2 is similar to that reported for more complex molecules that act by inducing IFN production.

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