A reducing redox environment promotes C2C12 myogenesis: Implications for regeneration in aged muscle

被引:95
作者
Hansen, Jason M.
Klass, Markus
Harris, Craig
Csete, Marie
机构
[1] Emory Univ, Sch Med, Dept Anesthesiol, Atlanta, GA 30322 USA
[2] Univ Michigan, Sch Publ Hlth, Toxicol Program, Dept Environm Hlth Sci, Ann Arbor, MI 48109 USA
关键词
C2C12; myoblast; muscle aging; myogenin; redox potential;
D O I
10.1016/j.cellbi.2006.11.027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intracellular redox potential of skeletal muscle becomes progressively more oxidized with aging, negatively impacting regenerative ability. We examined the effects of oxidizing redox potential on terminal differentiation of cultured C2C12 myoblasts. Redox potentials were manipulated by changing the culture O-2 environment, by free radical scavenging, or addition of H2O2. Intracellular reactive oxygen species (ROS) production was higher in 20% environmental O-2 and in this condition, redox potential became progressively oxidized compared to cultures in 6% O-2. Treatment with a ROS trapping agent (phenyl-N-tert-butylnitrone, PBN) caused reducing redox potentials and enhanced C2C12 differentiation, while addition of 25 micromolar H2O2 to cells in 20% O-2 dramatically slowed differentiation. Under these most oxidative conditions, quantitative PCR showed a significant decrease in myogenic basic helix-loop-helix transcription factor expression compared to cultures treated with PBN or grown in 6% O-2. Thus, oxidative intracellular environments impair myoblast differentiation, while reducing environments favor myogenesis. (c) 2006 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:546 / 553
页数:8
相关论文
共 35 条
  • [1] Balin A K, 1989, Clin Geriatr Med, V5, P1
  • [2] Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells
    Beauchamp, JR
    Heslop, L
    Yu, DSW
    Tajbakhsh, S
    Kelly, RG
    Wernig, A
    Buckingham, ME
    Partridge, TA
    Zammit, PS
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 151 (06) : 1221 - 1233
  • [3] MyoD and the transcriptional control of myogenesis
    Berkes, CA
    Tapscott, SJ
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (4-5) : 585 - 595
  • [4] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [5] Culture in low levels of oxygen enhances in vitro proliferation potential of satellite cells from old skeletal muscles
    Chakravarthy, MV
    Spangenburg, EE
    Booth, FW
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (08) : 1150 - 1158
  • [6] Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells
    Cornelison, DDW
    Wold, BJ
    [J]. DEVELOPMENTAL BIOLOGY, 1997, 191 (02) : 270 - 283
  • [7] Recent trends in glutathione biochemistry - Glutathione-protein interactions: A molecular link between oxidative stress and cell proliferation?
    Cotgreave, IA
    Gerdes, RG
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 242 (01) : 1 - 9
  • [8] Oxygen-mediated regulation of skeletal muscle satellite cell proliferation and adipogenesis in culture
    Csete, M
    Walikonis, J
    Slawny, N
    Wei, YW
    Korsnes, S
    Doyle, JC
    Wold, B
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 189 (02) : 189 - 196
  • [9] Dedieu S, 2002, INT J DEV BIOL, V46, P235
  • [10] FAULKNER JA, 1995, J GERONTOL A-BIOL, V50, P124