Mitochondrial DNA damage associated with lipid peroxidation of the mitochondrial membrane induced by Fe2+-citrate

被引:42
作者
Almeida, Andrea M.
机构
[1] Univ Estadual Campinas, Fac Ciencias Med, NCME, Dept Patol Clin, BR-13083970 Campinas, SP, Brazil
[2] Univ Fed Sao Paulo, CEDEME, Lab Controle Genet, BR-04023900 Sao Paulo, Brazil
[3] Univ Fed Vicosa, Dept Biol Vegetal, BR-36570000 Vicosa, MG, Brazil
[4] NIA, Lab Mol Gerontol, Baltimore, MD 21224 USA
来源
ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS | 2006年 / 78卷 / 03期
关键词
D O I
10.1590/S0001-37652006000300010
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Iron imbalance/accumulation has been implicated in oxidative injury associated with many degenerative diseases such as hereditary hemochromatosis, beta-thalassemia, and Friedreich's ataxia. Mitochondria are particularly sensitive to iron-induced oxidative stress - high loads of iron cause extensive lipid peroxidation and membrane permeabilization in isolated mitochondria. Here we detected and characterized mitochondrial DNA damage in isolated rat liver mitochondria exposed to a Fe2+-citrate complex, a small molecular weight complex. Intense DNA fragmentation was induced after the incubation of mitochondria with the iron complex. The detection of 3' phosphoglycolate ends at the mtDNA strand breaks by a P-32-postlabeling assay, suggested the involvement of hydroxyl radical in the DNA fragmentation induced by Fe2+-citrate. Increased levels of 8-oxo-7,8-dihydro-2'-deoxyguanosine also suggested that Fe2+-citrate-induced oxidative stress causes mitochondrial DNA damage. In conclusion, our results show that iron-mediated lipid peroxidation was associated with intense mtDNA damage derived from the direct attack of reactive oxygen species.
引用
收藏
页码:505 / 514
页数:10
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