Mitochondrial DNA depletion causes decreased ROS production and resistance to apoptosis

被引:21
作者
Chen, Hulin [1 ]
Wang, Junling [2 ]
Liu, Zhongrong [1 ]
Yang, Huilan [1 ]
Zhu, Yingjie [1 ]
Zhao, Minling [1 ]
Liu, Yan [1 ]
Yan, Miaomiao [1 ]
机构
[1] Liuhuaqiao Hosp, Guangzhou Mil Command, Guangzhou Gen Hosp, Dept Dermatol, 111 Liuhua Rd, Guangzhou 510010, Guangdong, Peoples R China
[2] Guangzhou Hosp Integrated Tradit & West Med, Gynecol Dept, Guangzhou 510800, Guangdong, Peoples R China
关键词
DNA depletion; mitochondrial; ultraviolet; apoptosis; reactive oxygen species; MUTATOR PHENOTYPE; OXIDATIVE STRESS; FREE-RADICALS; CYTOCHROME-C; ACTIVATION; MUTATIONS; TUMORS; CELLS; MOUSE; PROGRESSION;
D O I
10.3892/ijmm.2016.2697
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mitochondrial DNA (mtDNA) depletion occurs frequently in many diseases including cancer. The present study was designed in order to examine the hypothesis that mtDNA-depleted cells are resistant to apoptosis and to explore the possible mechanisms responsible for this effect. Parental human osteosarcoma 143B cells and mtDNA-deficient (Rho degrees or ?degrees) 206 cells (derived from 143B cells) were exposed to different doses of solar-simulated ultraviolet (UV) radiation. The effects of solar irradiation on cell morphology were observed under both light and fluorescence microscopes. Furthermore, apoptosis, mitochondrial membrane potential (MMP) disruption and reactive oxygen species (ROS) production were detected and measured by flow cytometry. In both cell lines, apoptosis and ROS production were clearly increased, whereas MMP was slightly decreased. However, apoptosis and ROS production were reduced in the Rho degrees 206 cells compared with the 143B cells. We also performed western blot analysis and demonstrated the increased release of cytosolic Cyt c from mitochondria in the 143B cells compared with that in the Rho degrees 206 cells. Thus, we concluded that Rho degrees 206 cells exhibit more resistance to solar-simulated UV radiation-induced apoptosis at certain doses than 143B cells and this is possibly due to decreased ROS production.
引用
收藏
页码:1039 / 1046
页数:8
相关论文
共 38 条
  • [31] Efficient repair of abasic sites in DNA by mitochondrial enzymes
    Pinz, KG
    Bogenhagen, DF
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) : 1257 - 1265
  • [32] Somatic mutations of the mitochondrial genome in human colorectal tumours
    Polyak, K
    Li, YB
    Zhu, H
    Lengauer, C
    Willson, JKV
    Markowitz, SD
    Trush, MA
    Kinzler, KW
    Vogelstein, B
    [J]. NATURE GENETICS, 1998, 20 (03) : 291 - 293
  • [33] Mitochondria-mediated nuclear mutator phenotype in Saccharomyces cerevisiae
    Rasmussen, AK
    Chatterjee, A
    Rasmussen, LJ
    Singh, KK
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (14) : 3909 - 3917
  • [34] Apoptosis-inducing effects of two anthraquinones from Hedyotis diffusa WILLD.
    Shi, Ying
    Wang, Chen-Hui
    Gong, Xing-Guo
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2008, 31 (06) : 1075 - 1078
  • [35] Attenuation of doxorubicin-induced contractile and mitochondrial dysfunction in mouse heart by cellular glutathione peroxidase
    Xiong, Ye
    Liu, Xuwan
    Lee, Chuan-Pu
    Chua, Balvin H. L.
    Ho, Ye-Shih
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2006, 41 (01) : 46 - 55
  • [36] Yamamoto Y, 2001, J DERMATOL SCI, V27, pS1
  • [37] Chemiluminescent detection and imaging of reactive oxygen species in live mouse skin exposed to UVA
    Yasui, H
    Sakurai, H
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 269 (01) : 131 - 136
  • [38] Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours
    Yeh, JJ
    Lunetta, KL
    van Orsouw, NJ
    Moore, FD
    Mutter, GL
    Vijg, J
    Dahia, PLM
    Eng, C
    [J]. ONCOGENE, 2000, 19 (16) : 2060 - 2066