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过氧化氢通过肝上皮 WB-F344 细胞中的溶血磷脂酸受体-3刺激细胞运动活性。

Hydrogen peroxide stimulates cell motile activity through LPA receptor-3 in liver epithelial WB-F344 cells.

机构信息

Division of Cancer Biology and Bioinformatics, Department of Life Science, Faculty of Science and Engineering, Kinki University, Higashiosaka, Osaka, Japan.

出版信息

Biochem Biophys Res Commun. 2013 Apr 12;433(3):317-21. doi: 10.1016/j.bbrc.2013.02.100. Epub 2013 Mar 16.

Abstract

Hydrogen peroxide which is one of reactive oxygen species (ROS) mediates a variety of biological responses, including cell proliferation and migration. In the present study, we investigated whether lysophosphatidic acid (LPA) signaling is involved in cell motile activity stimulated by hydrogen peroxide. The rat liver epithelial WB-F344 cells were treated with hydrogen peroxide at 0.1 or 1 μM for 48 h. In cell motility assays, hydrogen peroxide treated cells showed significantly high cell motile activity, compared with untreated cells. To measure the expression levels of LPA receptor genes, quantitative real time RT-PCR analysis was performed. The expressions of LPA receptor-3 (Lpar3) in hydrogen peroxide treated cells were significantly higher than those in control cells, but not Lpar1 and Lpar2 genes. Next, to assess the effect of LPA3 on cell motile activity, the Lpar3 knockdown cells from WB-F344 cells were also treated with hydrogen peroxide. The cell motile activity of the knockdown cells was not stimulated by hydrogen peroxide. Moreover, in liver cancer cells, hydrogen peroxide significantly activated cell motility of Lpar3-expressing cells, but not Lpar3-unexpressing cells. These results suggest that LPA signaling via LPA3 may be mainly involved in cell motile activity of WB-F344 cells stimulated by hydrogen peroxide.

摘要

过氧化氢是活性氧(ROS)的一种,介导多种生物学反应,包括细胞增殖和迁移。在本研究中,我们研究了溶血磷脂酸(LPA)信号是否参与过氧化氢刺激的细胞迁移活性。用 0.1 或 1 μM 过氧化氢处理大鼠肝上皮 WB-F344 细胞 48 h。在细胞迁移实验中,与未处理细胞相比,过氧化氢处理的细胞表现出明显更高的细胞迁移活性。为了测量 LPA 受体基因的表达水平,进行了定量实时 RT-PCR 分析。与对照细胞相比,过氧化氢处理的细胞中 LPA 受体-3(Lpar3)的表达显著升高,但 Lpar1 和 Lpar2 基因没有变化。接下来,为了评估 LPA3 对细胞迁移活性的影响,还从 WB-F344 细胞中敲低了 Lpar3 的细胞用过氧化氢处理。敲低细胞的细胞迁移活性不受过氧化氢刺激。此外,在肝癌细胞中,过氧化氢显著激活了 Lpar3 表达细胞的细胞迁移活性,但不激活 Lpar3 非表达细胞。这些结果表明,LPA 信号通过 LPA3 可能主要参与过氧化氢刺激的 WB-F344 细胞的细胞迁移活性。

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