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首页> 外文期刊>Journal of pharmacological sciences. >Dictyostelium Differentiation-Inducing Factor-1 Binds to Mitochondrial Malate Dehydrogenase and Inhibits Its Activity
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Dictyostelium Differentiation-Inducing Factor-1 Binds to Mitochondrial Malate Dehydrogenase and Inhibits Its Activity

机译:Dictyostelium分化诱导因子1绑定到线粒体苹果酸脱氢酶并抑制其活性。

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摘要

References(26) Cited-By(5) We have reported that the differentiation-inducing factors (DIFs) DIF-1 and DIF-3, morphogens secreted from Dictyostelium discoideum, inhibit proliferation of several cancer cells via suppression of the Wnt/β-catenin signaling pathway. However, the target molecules of DIFs involved in the anti-proliferative effects are still unknown. In the present study, DIF-1–tethered resins were synthesized to explore the target molecules of DIFs, and mitochondrial malate dehydrogenase (mMDH) was identified as one of the target molecules. In the in vitro assay, DIF-1 and other analogs including 2-MIDIF-1, DIF-3, and 6-MIDIF-3 were found to be capable of binding to mMDH but not to cytoplasmic MDH. However, only DIF-1 and 2-MIDIF-1 inhibited the enzymatic activity of mMDH. The effects of DIF analogs on ATP content and cell proliferation were then analyzed using HeLa cells. DIF-1 and 2-MIDIF-1 were found to lower the ATP content and both chemicals inhibited HeLa cell proliferation, suggesting that inhibition of mMDH activity affected cell energy production, probably leading to the inhibition of proliferation. These results suggest that the inhibition of mMDH activity by DIF-1 and 2-MIDIF-1 could be one of the mechanisms to induce anti-proliferative effects, independent of the inhibition of the Wnt/β-catenin signaling pathway.
机译:参考文献(26)Cited-By(5)我们已经报道了Discoyostelium discoideum分泌的形态发生因子分化诱导因子(DIFs)DIF-1和DIF-3通过抑制Wnt /β-来抑制几种癌细胞的增殖。连环蛋白信号通路。但是,参与抗增殖作用的DIF的靶分子仍然是未知的。在本研究中,合成了DIF-1束缚树脂以探索DIF的目标分子,并且线粒体苹果酸脱氢酶(mMDH)被确定为目标分子之一。在体外测定中,发现DIF-1和其他类似物(包括2-MIDIF-1,DIF-3和6-MIDIF-3)能够与mMDH结合,但不与细胞质MDH结合。但是,只有DIF-1和2-MIDIF-1抑制mMDH的酶活性。然后使用HeLa细胞分析DIF类似物对ATP含量和细胞增殖的影响。发现DIF-1和2-MIDIF-1降低了ATP含量,并且两种化学物质均抑制HeLa细胞增殖,这表明抑制mMDH活性会影响细胞的能量产生,可能导致增殖抑制。这些结果表明,DIF-1和2-MIDIF-1对mMDH活性的抑制可能是诱导抗增殖作用的机制之一,而与Wnt /β-catenin信号通路的抑制无关。

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