Cytotoxicity of iron (III), molybdenum (III), and their mixtures in BALB/3T3 and HepG2 cells

被引:20
作者
Terpilowska, Sylwia [1 ]
Siwicka-Gieroba, Dorota [2 ]
Siwicki, Andrzej Krzysztof [3 ]
机构
[1] John Paul II Catholic Univ Lublin, Inst Environm Engn, Lab Environm Biol, PL-20950 Lublin, Poland
[2] Med Univ Lublin, Fac Med, Dept Anaesthesiol & Intens Care, PL-20850 Lublin, Poland
[3] Univ Warmia & Mazury, Fac Vet Med, Dept Microbiol & Clin Immunol, PL-10957 Olsztyn, Poland
关键词
molybdenum (III); iron (III); cytotoxicity; interactions; IN-VITRO; OXIDATIVE STRESS; TOXICITY; NANOPARTICLES; GENOTOXICITY; METABOLISM; APOPTOSIS; ASSAYS; LINE; RED;
D O I
10.2478/jvetres-2018-0066
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Introduction: Iron and molybdenum are essential trace elements for cell metabolism. They are involved in maintaining proper functions of enzymes, cell proliferation, and metabolism of DNA. Material and Methods: BALB/3T3 and HepG2 cells were incubated with iron chloride or molybdenum trioxide at concentrations from 100 to 1,400 mu M. The cells were also incubated in mixtures of iron chloride at 200 mu M plus molybdenum trioxide at 1,000 mu M or iron chloride at 1,000 mu M plus molybdenum trioxide at 200 mu M. Cell viability was determined with MTT reduction, LHD release, and NRU tests. Results: A decrease in cell viability was observed after incubating both cell lines with iron chloride or molybdenum trioxide. In cells incubated with mixtures of these trace elements, a decrease in cell viability was observed, assessed by all the used assays. Conclusions: Iron (III) and molybdenum (III) decrease cell viability in normal and cancer cells. A synergistic effect of the mixture of these elements was observed.
引用
收藏
页码:527 / 533
页数:7
相关论文
共 21 条
  • [1] Cellular responses induced in vitro by iron (Fe) in a central nervous system cell line (U343MGa)
    Alcantara, D. D. F. A.
    Ribeiro, H. F.
    Matos, L. A.
    Sousa, J. M. C.
    Burbano, R. R.
    Bahia, M. O.
    [J]. GENETICS AND MOLECULAR RESEARCH, 2013, 12 (02) : 1554 - 1560
  • [2] In vitro cytotoxicity of nanoparticles in mammalian germline stem cells
    Braydich-Stolle, L
    Hussain, S
    Schlager, JJ
    Hofmann, MC
    [J]. TOXICOLOGICAL SCIENCES, 2005, 88 (02) : 412 - 419
  • [3] New studies on the in vitro genotoxicity of sodium molybdate and their impact on the overall assessment of the genotoxicity of molybdenum substances
    Burzlaff, Arne
    Beevers, Carol
    Pearce, Helen
    Lloyd, Melvyn
    Klipsch, Kevin
    [J]. REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2017, 86 : 279 - 291
  • [4] Simultaneous evaluation of cell viability by neutral red, MTT and crystal violet staining assays of the same cells
    Chiba, K
    Kawakami, K
    Tohyama, K
    [J]. TOXICOLOGY IN VITRO, 1998, 12 (03) : 251 - 258
  • [5] Iron mediated toxicity and programmed cell death: A review and a re-examination of existing paradigms
    Eid, Rawan
    Arab, Nagla T. T.
    Greenwood, Michael T.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2017, 1864 (02): : 399 - 430
  • [6] Long-Term Exposure to Zidovudine Delays Cell Cycle Progression, Induces Apoptosis, and Decreases Telomerase Activity in Human Hepatocytes
    Fang, Jia-Long
    Beland, Frederick A.
    [J]. TOXICOLOGICAL SCIENCES, 2009, 111 (01) : 120 - 130
  • [7] Availability and toxicity of Fe(II) and Fe(III) in Caco-2 cells
    He, Wan-ling
    Feng, Ying
    Li, Xiao-li
    Wei, Yan-yan
    Yang, Xiao-e
    [J]. JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2008, 9 (09): : 707 - 712
  • [8] In vitro toxicity of nanoparticles in BRL 3A rat liver cells
    Hussain, SM
    Hess, KL
    Gearhart, JM
    Geiss, KT
    Schlager, JJ
    [J]. TOXICOLOGY IN VITRO, 2005, 19 (07) : 975 - 983
  • [9] Body iron metabolism and pathophysiology of iron overload
    Kohgo, Yutaka
    Ikuta, Katsuya
    Ohtake, Takaaki
    Torimoto, Yoshihiro
    Kato, Junji
    [J]. INTERNATIONAL JOURNAL OF HEMATOLOGY, 2008, 88 (01) : 7 - 15
  • [10] In vitro setting of dose-effect relationships of 32 metal compounds in the Balb/3T3 cell line, as a basis for predicting their carcinogenic potential
    Mazzotti, F
    Sabbioni, E
    Ponti, J
    Ghiani, M
    Fortaner, S
    Rossi, GL
    [J]. ATLA-ALTERNATIVES TO LABORATORY ANIMALS, 2002, 30 (02): : 209 - 217