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首页> 外文期刊>Acta histochemica et cytochemica. >Estrogen Regulates Mitochondrial Morphology through Phosphorylation of Dynamin-related Protein 1 in MCF7 Human Breast Cancer Cells
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Estrogen Regulates Mitochondrial Morphology through Phosphorylation of Dynamin-related Protein 1 in MCF7 Human Breast Cancer Cells

机译:雌激素通过磷酸化动力蛋白相关蛋白1在MCF7人乳腺癌细胞中调节线粒体形态。

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摘要

Estrogen affects mitochondrial function in various tissues, but the precise mechanism remains unclear. We, therefore investigated the effect on estrogen-regulated mitochondrial morphology by dynamin-related protein 1 (Drp1) and its Ser616-phosphorylated derivative (pDrp1Ser616) are involved in mitochondrial fission. MCF7 human breast cancer cells were treated with 17β-estradiol (E2), an estrogen receptor (ER) α and β antagonist (ICI 182, 780), an ERα antagonist (MPP), and an ERβ antagonist (PHTPP) for 24 hr. The expression of Drp1 and pDrp1Ser616 was analyzed by western blotting and immunohistochemistry. Mitochondrial morphology was analyzed by transmission electron microscopy (TEM). In control cells, Drp1 was detected in the cytoplasm of all cells while pDrp1 was observed in the cytoplasm of 3.4 ± 1.0% of the total population. After E2 treatment, pDrp1Ser616-positive cells comprised 30.6 ± 5.6% of the total population, 10.5 ± 1.7% after E2 + ICI treatment, 12.4 ± 4.2% after E2 + MPP treatment, and 24.0 ± 2.2% after E2 + PHTPP treatment. In ERα knockdown MCF7 cells, pDrp1 expression was decreased after E2 treatment compared to E2-treated wild type cells. Tubular pattern mitochondria were found in the control cells but the number of short and small pattern mitochondria (2) was significantly increased after E2 treatment (as observed by TEM). We, therefore concluded that the phosphorylation of Drp1 is important for E2-dependent mitochondrial morphological changes through ERα.
机译:雌激素影响各种组织中的线粒体功能,但确切机制尚不清楚。因此,我们研究了动力蛋白相关蛋白1(Drp1)及其Ser616磷酸化衍生物(pDrp1 Ser616 )参与线粒体裂变对雌激素调节的线粒体形态的影响。使用17β-雌二醇(E 2 ),雌激素受体(ER)α和β拮抗剂(ICI 182、780),ERα拮抗剂(MPP)和ERβ处理MCF7人乳腺癌细胞拮抗剂(PHTPP)24小时。 Western blotting和免疫组化分析Drp1和pDrp1 Ser616 的表达。通过透射电子显微镜(TEM)分析线粒体形态。在对照细胞中,在所有细胞的细胞质中检测到Drp1,而在细胞质中观察到pDrp1,占总群体的3.4±1.0%。经E 2 处理后,pDrp1 Ser616 阳性细胞占总种群的30.6±5.6%,经过E 2 + ICI后为10.5±1.7% E 2 + MPP治疗后为12.4±4.2%,E 2 + PHTPP治疗后为24.0±2.2%。在ERα敲低的MCF7细胞中,与E 2 处理后的野生型细胞相比,E 2 处理后pDrp1表达降低。对照细胞中发现管状模式的线粒体,但E 2 处理后短和小的模式线粒体(2 )的数量显着增加(通过TEM观察)。因此,我们得出结论,Drp1的磷酸化对于通过ERα依赖E 2 的线粒体形态变化非常重要。

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