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首页> 外文期刊>Biochemical and Biophysical Research Communications >Different effects of G -protein -coupled receptor 120 (GPR120) and GPR40 on cell motile activity of highly migratory osteosarcoma cells
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Different effects of G -protein -coupled receptor 120 (GPR120) and GPR40 on cell motile activity of highly migratory osteosarcoma cells

机译:G-普选蛋白-coupled受体120(GPR120)和GPR40对高度迁移骨肉瘤细胞的细胞运动活性的不同效果

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G-protein-coupled receptor 120 (GPR120) and GPR40 are members of free fatty acid (FFA) receptors and mediate a variety of biological responses through binding of medium- and long -chain FFAs. Recently, it has been reported that GPR120 and GPR40 regulated cellular functions of cancer cells. In the present study, to assess whether GPR120 and GPR40 are involved in the enhancement of cell motile activity of osteosarcoma cells, we established highly migratory (MG63-R7) cells from osteosarcoma MG -63 cells. The expression level of GPR120 gene was significantly higher in MG63-R7 cells than in MG -63 cells, while no change of GPR40 expression was observed. In cell motility assay, the cell motile activity of MG63-R7 cells was approximately 200 times higher than that of MG-63 cells. The cell motile activity of MG63-R7 cells was stimulated by GW9508, which is an agonist of GPR120 and GPR40. Moreover, a GPR40 antagonist GW1100 elevated the cell motile activity of MG63-R7 cells in the presence of GW9508. To confirm the effects of GPR120 and GPR40 on the cell motile activity of MG63-R7 cells, GPR120 knockdown cells were generated from MG63-R7 cells. The cell motile activity of MG63-R7 cells was markedly suppressed by GPR120 knockdown. These results indicated that GPR120 enhanced and GPR40 inhibited the cell motile activity of highly migratory osteosarcoma cells. (C) 2017 Elsevier Inc. All rights reserved.
机译:G蛋白偶联受体120(GPR120)和GPR40是游离脂肪酸(FFA)受体的成员,并通过中等和长型FFA的结合介导各种生物反应。最近,据报道,GPR120和GPR40调节癌细胞的细胞功能。在本研究中,为了评估GPR120和GPR40是否参与骨肉瘤细胞的细胞运动活性的增强,我们从骨肉瘤MG -63细胞建立了高度迁移(Mg6-R7)细胞。 Mg63-R7细胞中GPR120基因的表达水平明显高于Mg -63细胞,而观察到GPR40表达的变化。在细胞运动测定中,Mg63-R7细胞的细胞运动活性约为比Mg-63细胞高的200倍。 Mg63-R7细胞的细胞运动活性由GW9508刺激,其是GPR120和GPR40的激动剂。此外,GPR40拮抗剂GW1100在GW9508的存在下升高了Mg63-R7细胞的细胞运动活性。为了确认GPR120和GPR40对Mg63-R7细胞的细胞运动活性的影响,从Mg63-R7细胞产生GPR120敲低细胞。通过GPR120敲低表示Mg63-R7细胞的细胞运动活性。这些结果表明,GPR120增强和GPR40抑制高度迁移骨肉瘤细胞的细胞运动活性。 (c)2017年Elsevier Inc.保留所有权利。

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