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Inhibition of ERK oscillations by ionizing radiation and reactive oxygen species.

机译:通过电离辐射和活性氧物质抑制ERK振荡。

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The shuttling of activated protein kinases between the cytoplasm and nucleus is an essential feature of normal growth factor signaling cascades. Here we demonstrate that transforming growth factor alpha (TGFalpha) induces oscillations in extracellular signal regulated kinase (ERK) cytoplasmic-nuclear translocations in human keratinocytes. TGFalpha-dependent ERK oscillations mediated through the epidermal growth factor receptor (EGFR) are inhibited by low dose X-irradiation (10 cGy) and low concentrations of hydrogen peroxide (0.32-3.26 microM H(2)O(2)) used as a model reactive oxygen species (ROS). A fluorescent indicator dye (H2-DCFDA) was used to measure cellular ROS levels following X-irradiation, 12-O-tetradecanoyl phorbol-13-acetate (TPA) and H(2)O(2). X-irradiation did not generate significant ROS production while 0.32 microM H(2)O(2) and TPA induced significant increases in ROS levels with H(2)O(2) > TPA. TPA alone induced transactivation of the EGFR but did not induce ERK oscillations. TPA as a cotreatment did not inhibit TGFalpha-stimulated ERK oscillations but qualitatively altered TGFalpha-dependent ERK oscillation characteristics (amplitude, time-period). Collectively, these observations demonstrate that TGFalpha-induced ERK oscillations are inhibited by ionizing radiation/ROS and perturbed by epigenetic carcinogen in human keratinocytes.
机译:活化蛋白激酶在细胞质和细胞核之间的穿梭是正常生长因子信号转导级联的基本特征。在这里,我们证明了转化生长因子α(TGFalpha)在人角质形成细胞中诱导细胞外信号调节激酶(ERK)细胞质-核易位的振荡。通过表皮生长因子受体(EGFR)介导的TGFalpha依赖性ERK振荡被低剂量X射线辐射(10 cGy)和低浓度的过氧化氢(0.32-3.26 microM H(2)O(2))抑制模拟活性氧(ROS)。荧光指示剂染料(H2-DCFDA)用于测量X射线,12-O-十四烷酰佛波醇13-乙酸盐(TPA)和H(2)O(2)后的细胞ROS水平。 X射线辐射不会产生明显的ROS产生,而0.32 microM H(2)O(2)和TPA会导致H(2)O(2)> TPA引起的ROS水平显着增加。单独的TPA诱导EGFR的反式激活,但不诱导ERK振荡。 TPA作为辅助治疗不会抑制TGFα刺激的ERK振荡,但会定性改变TGFα依赖性的ERK振荡特征(幅度,时间)。总而言之,这些观察结果表明,TGFalpha诱导的ERK振荡受到电离辐射/ ROS的抑制,并受到人角质形成细胞中表观遗传致癌物的干扰。

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