Oo Phyu Synn, Yamaguchi Yuya, Sawaguchi Akira, Tin Htwe Kyaw Myat, Choijookhuu Narantsog, Noor Ali Mohmand, Srisowanna Naparee, Hino Shin-Ichiro, Hishikawa Yoshitaka
Department of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan.
Department of Anatomy, Ultrastructural Cell Biology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan.
Acta Histochem Cytochem. 2018 Feb 27;51(1):21-31. doi: 10.1267/ahc.17034. Epub 2018 Feb 21.
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 (pDrp1) are involved in mitochondrial fission. MCF7 human breast cancer cells were treated with 17β-estradiol (E), 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 pDrp1 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 E treatment, pDrp1-positive cells comprised 30.6 ± 5.6% of the total population, 10.5 ± 1.7% after E + ICI treatment, 12.4 ± 4.2% after E + MPP treatment, and 24.0 ± 2.2% after E + PHTPP treatment. In ERα knockdown MCF7 cells, pDrp1 expression was decreased after E treatment compared to E-treated wild type cells. Tubular pattern mitochondria were found in the control cells but the number of short and small pattern mitochondria (< 0.5 μm) was significantly increased after E treatment (as observed by TEM). We, therefore concluded that the phosphorylation of Drp1 is important for E-dependent mitochondrial morphological changes through ERα.
雌激素会影响多种组织中的线粒体功能,但其确切机制仍不清楚。因此,我们研究了与发动蛋白相关蛋白1(Drp1)及其丝氨酸616磷酸化衍生物(pDrp1)对雌激素调节的线粒体形态的影响,它们参与线粒体分裂。MCF7人乳腺癌细胞用17β-雌二醇(E)、雌激素受体(ER)α和β拮抗剂(ICI 182,780)、ERα拮抗剂(MPP)和ERβ拮抗剂(PHTPP)处理24小时。通过蛋白质印迹法和免疫组织化学分析Drp1和pDrp1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均检测到Drp1,而在总细胞群体的3.4±1.0%的细胞质中观察到pDrp1。E处理后,pDrp1阳性细胞占总细胞群体的30.6±5.6%,E+ICI处理后为10.5±1.7%,E+MPP处理后为12.4±4.2%,E+PHTPP处理后为24.0±2.2%。在ERα敲低的MCF7细胞中,与E处理的野生型细胞相比,E处理后pDrp1表达降低。在对照细胞中发现了管状模式的线粒体,但E处理后短而小的模式线粒体(<0.5μm)的数量显著增加(通过TEM观察)。因此,我们得出结论,Drp1的磷酸化对于通过ERα的E依赖性线粒体形态变化很重要。