TFAM-dependent and independent dynamics of mtDNA levels in C2C12 myoblasts caused by redox stress

被引:28
作者
Noack, H [1 ]
Bednarek, T [1 ]
Heidler, J [1 ]
Ladig, R [1 ]
Holtz, J [1 ]
Szibor, M [1 ]
机构
[1] Univ Halle Wittenberg, Inst Pathophysiol, ZAMED, D-06097 Halle, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2006年 / 1760卷 / 02期
关键词
TFAM; mtTFA; mtDNA; regeneration; proliferation; redox stress;
D O I
10.1016/j.bbagen.2005.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TFAM is an essential protein factor for the initiation of transcription of the mtDNA. It also functions as a packaging factor, which stabilizes the mtDNA pool. To investigate the regulatory role of TFAM for regeneration and proliferation of the mtDNA pool, we exposed the muscle cell line C2C12 to a severe redox stress (H2O2) or to a moderate redox stress (GSH depletion), determined the dynamics of the mtDNA levels and correlated this with the TFAM protein levels. H2O2 caused a concentration-dependent loss of mtDNA molecules. The mtDNA levels recovered slowly within 3 days after H2O2 stress. The TFAM protein was less degraded than the mtDNA indicating an accumulation of TFAM protein per mtDNA after H2O2 stress. Overexpression of TFAM did not protect against the mtDNA loss after H2O2 stress but shortened the recovery time. GSH depletion led to a proliferation of the mtDNA pool. Although the mtDNA levels increased the TFAM protein levels were unaffected by the GSH depletion. We conclude that the accumulation of the TFAM protein after H2O2 stress contributes to the regeneration of the mtDNA pool but that other mechanisms, independent from the TFAM protein amount have to be postulated to explain the proliferation of the mtDNA pool after GSH depletion. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 150
页数:10
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