Stress defense in murine embryonic stem cells is superior to that of various differentiated murine cells

被引:221
作者
Saretzki, G
Armstrong, L
Leake, A
Lako, M
von Zglinicki, T [1 ]
机构
[1] Newcastle Univ, Newcastle Gen Hosp, Henry Wellcome Lab Biogerontol, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[2] Newcastle Univ, Newcastle Gen Hosp, Inst Human Genet, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[3] Univ Durham, Dept Biol Sci, Durham, NC USA
关键词
D O I
10.1634/stemcells.22-6-962
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A very small number of embryonic stem (ES) cells gives rise to all tissues of the embryo proper. This means that ES cells should be equipped with highly efficient mechanisms to defend themselves against various stresses and to prevent or repair DNA damage. One of these mechanisms is a high activity of a verapamil-sensitive multidrug efflux pump. Because reactive oxygen species are a major source of DNA damage, we further tested the idea that murine ES cells might differ from their more differentiated counterparts by high levels of antioxidant defense and good DNA strand break repair capacity. This was confirmed by comparing cellular peroxide levels, total antioxidant capacity, and activity of radiation-induced strand break repair between murine ES cells and embryoid bodies or embryonic fibroblasts. Using microarrays and confirmation by reverse transcription-polymerase chain reaction, we identified several candidate antioxidant and stress-resistance genes that become downregulated during differentiation of ES cells into embryoid bodies.
引用
收藏
页码:962 / 971
页数:10
相关论文
共 47 条
  • [1] ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage
    Aladjem, MI
    Spike, BT
    Rodewald, LW
    Hope, TJ
    Klemm, M
    Jaenisch, R
    Wahl, GM
    [J]. CURRENT BIOLOGY, 1998, 8 (03) : 145 - 155
  • [2] mTert expression correlates with telomerase activity during the differentiation of murine embryonic stem cells
    Armstrong, L
    Lako, M
    Lincoln, J
    Cairns, PM
    Hole, N
    [J]. MECHANISMS OF DEVELOPMENT, 2000, 97 (1-2) : 109 - 116
  • [3] STAGE-SPECIFIC REGULATION OF MURINE HSP68 GENE PROMOTER IN PREIMPLANTATION MOUSE EMBRYOS
    BEVILACQUA, A
    KINNUNEN, LH
    BEVILACQUA, S
    MANGIA, F
    [J]. DEVELOPMENTAL BIOLOGY, 1995, 170 (02) : 467 - 478
  • [4] BIRNBOIM HC, 1981, CANCER RES, V41, P1889
  • [5] L-selegiline potentiates the cellular poly(ADP-ribosyl)ation response to ionizing radiation
    Brabeck, C
    Pfeiffer, R
    Leake, A
    Beneke, S
    Meyer, R
    Bürkle, A
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 306 (03) : 973 - 979
  • [6] ABC transporters as phenotypic markers and functional regulators of stem cells
    Bunting, KD
    [J]. STEM CELLS, 2002, 20 (01) : 11 - 20
  • [7] Oxygen accelerates the accumulation of mutations during the senescence and immortalization of murine cells in culture
    Busuttil, RA
    Rubio, M
    Dollé, MET
    Campisi, J
    Vijg, J
    [J]. AGING CELL, 2003, 2 (06) : 287 - 294
  • [8] Implication of PBP74/mortalin/GRP75 in the radio-adaptive response
    Carette, J
    Lehnert, S
    Chow, TYK
    [J]. INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2002, 78 (03) : 183 - 190
  • [9] P53-dependent and -independent links between DNA-damage, apoptosis and mutation frequency in ES cells
    Corbet, SW
    Clarke, AR
    Gledhill, S
    Wyllie, AH
    [J]. ONCOGENE, 1999, 18 (08) : 1537 - 1544
  • [10] An imbalance in antioxidant defense affects cellular function: the pathophysiological consequences of a reduction in antioxidant defense in the glutathione peroxidase-1 (Gpx1) knockout mouse
    de Haan, JB
    Crack, PJ
    Flentjar, N
    Iannello, RC
    Hertzog, PJ
    Kola, I
    [J]. REDOX REPORT, 2003, 8 (02) : 69 - 79