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首页> 外文期刊>Nutrients >A Novel Role for a Major Component of the Vitamin D Axis: Vitamin D Binding Protein-Derived Macrophage Activating Factor Induces Human Breast Cancer Cell Apoptosis through Stimulation of Macrophages
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A Novel Role for a Major Component of the Vitamin D Axis: Vitamin D Binding Protein-Derived Macrophage Activating Factor Induces Human Breast Cancer Cell Apoptosis through Stimulation of Macrophages

机译:维生素D轴主要成分的新型作用:维生素D结合蛋白衍生的巨噬细胞活化因子通过刺激巨噬细胞诱导人乳腺癌细胞凋亡。

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摘要

The role of vitamin D in maintaining health appears greater than originally thought, and the concept of the vitamin D axis underlines the complexity of the biological events controlled by biologically active vitamin D (1,25(OH)(2)D3), its two binding proteins that are the vitamin D receptor (VDR) and the vitamin D-binding protein-derived macrophage activating factor (GcMAF). In this study we demonstrate that GcMAF stimulates macrophages, which in turn attack human breast cancer cells, induce their apoptosis and eventually phagocytize them. These results are consistent with the observation that macrophages infiltrated implanted tumors in mice after GcMAF injections. In addition, we hypothesize that the last 23 hydrophobic amino acids of VDR, located at the inner part of the plasma membrane, interact with the first 23 hydrophobic amino acids of the GcMAF located at the external part of the plasma membrane. This al1ows 1,25(OH)(2)D3 and oleic acid to become sandwiched between the two vitamin D-binding proteins, thus postulating a novel molecular mode of interaction between GcMAF and VDR. Taken together, these results support and reinforce the hypothesis that GcMAF has multiple biological activities that could be responsible for its anti-cancer effects, possibly through molecular interaction with the VDR that in turn is responsible for a multitude of non-genomic as well as genomic effects.
机译:维生素D在维持健康方面的作用似乎比最初想像的要强,并且维生素D轴的概念强调了由具有生物活性的维生素D(1,25(OH)(2)D3),这两个维生素D控制的生物事件的复杂性维生素D受体(VDR)和维生素D结合蛋白衍生的巨噬细胞活化因子(GcMAF)的结合蛋白。在这项研究中,我们证明GcMAF刺激巨噬细胞,进而攻击人乳腺癌细胞,诱导其凋亡并最终吞噬它们。这些结果与在注射GcMAF后巨噬细胞浸润小鼠的植入肿瘤的观察结果一致。另外,我们假设位于质膜内部的VDR的最后23个疏水氨基酸与位于质膜外部的GcMAF的前23个疏水氨基酸相互作用。这允许1,25(OH)(2)D3和油酸夹在两个维生素D结合蛋白之间,从而推测了GcMAF和VDR之间相互作用的新型分子模式。综上所述,这些结果支持并加强了以下假设:GcMAF具有多种生物学活性,可能是其抗癌作用的原因,可能是通过与VDR的分子相互作用而引起的,VDR进而导致了许多非基因组和基因组效果。

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