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Nitric Oxide Is Important for Mouse Beta-Cell Line Killing by Peritoneal Exudate Cells Obtained from Cyclophosphamide Treated Non-Obese Diabetic Mice

机译:一氧化氮对于由环磷酰胺治疗的非肥胖糖尿病小鼠的腹膜分泌液杀死小鼠β细胞系很重要

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References(29) Cited-By(1) Macrophages from recent onset non-obese diabetic (NOD) mice showed cytotoxicity against the NOD mouse derived beta-cell line, MIN6N-9a. In this report, we examined whether nitric oxide is associated with beta-cell destruction. Peritoneal exudate cells (PEC), obtained from cyclophosphamide treated NOD mice showed higher cytotoxicity against MIN6N-9a compared to PECs from saline injected NOD mice (P0.01). This effect was suppressed in cells incubated with 0.5mmol/lNG-methyl-L-arginine, a nitric oxide synthase inhibitor (P0.001). In addition, the nitrite concentration of the co-culture medium, as an index of nitric oxide production, increased in MIN6N-9a cells co-cultured with peritoneal exudate cells from cyclophosphamide injected NOD mice but not in co-culture with saline injected NOD mice (P0.05). Thus, nitric oxide plays an important role in beta-cell line destruction of macrophages obtained from NOD mice.
机译:参考文献(29)来自最近发作的非肥胖糖尿病(NOD)小鼠的被引用的By(1)巨噬细胞显示出对NOD小鼠衍生的β细胞系MIN6N-9a的细胞毒性。在本报告中,我们检查了一氧化氮是否与β细胞破坏有关。与经盐水注射的NOD小鼠的PEC相比,从环磷酰胺处理的NOD小鼠获得的腹膜分泌液(PEC)对MIN6N-9a具有更高的细胞毒性(P <0.01)。在用一氧化氮合酶抑制剂0.5mmol / lNG-甲基-L-精氨酸孵育的细胞中抑制了这种作用(P <0.001)。此外,共培养培养基中亚硝酸盐的浓度(作为一氧化氮产生的指标)在与环磷酰胺注射的NOD小鼠腹膜渗出液共培养的MIN6N-9a细胞中增加,但在与盐水注射的NOD小鼠共培养中却没有增加(P <0.05)。因此,一氧化氮在从NOD小鼠获得的巨噬细胞的β细胞系破坏中起重要作用。

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