Uitendaal M P, Thijssen H H, Drittij-Reijnders M J, Hoeijmakers M J
Biochem Biophys Res Commun. 1986 Jun 30;137(3):1015-20. doi: 10.1016/0006-291x(86)90326-8.
Using an adapted assay that requires an enzyme aliquot that forms only 5 pmoles vitamin K, we were able to demonstrate vitamin K1 2,3 epoxide reductase activity in cultured B16 mouse melanoma cells. The enzyme uses dithiothreitol, but not NADH as a reducing cofactor and is sensitive to inhibition by warfarin (2% residual activity at 10 micrograms/ml warfarin). Incubation of B16 cells in culture with 30 micrograms/ml warfarin leads to an 45% residual reductase as compared to normally cultured B16 cells. Combined with the reported presence of vitamin K dependent carboxylase in B16 cells and the cytotoxicity of warfarin towards B16 cells this suggests an active vitamin K cycle in these melanoma cells that may be essential for survival.
使用一种经过改良的检测方法,该方法需要一份仅能形成5皮摩尔维生素K的酶等分试样,我们能够在培养的B16小鼠黑色素瘤细胞中证明维生素K1 2,3-环氧化物还原酶活性。该酶使用二硫苏糖醇而非NADH作为还原辅因子,并且对华法林的抑制作用敏感(在10微克/毫升华法林浓度下残留活性为2%)。与正常培养的B16细胞相比,将培养的B16细胞与30微克/毫升华法林一起孵育会导致残留还原酶为45%。结合报道中B16细胞中存在维生素K依赖性羧化酶以及华法林对B16细胞的细胞毒性,这表明这些黑色素瘤细胞中存在一个活跃的维生素K循环,这可能对细胞存活至关重要。