Hypomethylation of mitochondrial D-loop and ND6 with increased mitochondrial DNA copy number in the arsenic-exposed population

被引:55
作者
Sanyal, Tamalika [1 ,3 ]
Bhattacharjee, Pritha [1 ,3 ]
Bhattacharjee, Sandip [2 ]
Bhattacharjee, Pritha [1 ,3 ]
机构
[1] Univ Calcutta, Dept Zool, Kolkata 700019, India
[2] Siemens, Hlth Management Occupat Hlth, Bombay, Maharashtra, India
[3] Univ Calcutta, Dept Environm Sci, Kolkata 700019, India
关键词
Arsenic toxicity; Mitochondrial DNA methylation; D-loop; ND6; Mitochondrial DNA copy number; INDUCED SKIN-LESIONS; OXIDATIVE STRESS; METHYLATION PATTERN; DAMAGE; CELLS; INDIVIDUALS; EXPRESSION; DISEASE; REGION; REVERSIBILITY;
D O I
10.1016/j.tox.2018.06.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Groundwater arsenic contamination has become a serious global concern due to its adverse effects on human health. Arsenic-induced reactive oxygen species trigger oxidative stress inside mitochondria, which initiate a cascade of events including altered mitochondrial (mt) membrane potential, uncoupling of electron transport chain, and mtDNA damage. A case-control study was conducted to examine the association between arsenic exposure and differences in mtDNA methylation and to assess the downstream consequences. We recruited 221 arsenic-exposed individuals, including 106 individuals with skin lesions (WSL) and 115 subjects without any skin lesions (WOSL) from the Murshidabad district, West Bengal, India. The unexposed group included 101 individuals from the arsenic unexposed area in East Midnapore. We analyzed the status of mtDNA methylation in D-loop region and ND6 gene by methylation-specific PCR. Gene expression was studied by quantitative real-time PCR. Significant hypomethylation in both D-loop and ND6 was observed with a consequent increase in their target gene expression and higher mtDNA copy number in arsenic-exposed populations compared to controls. Further mechanistic insights regarding mitochondrial epigenetic alteration in arsenic exposure will be of critical importance for the prevention of adverse health effects.
引用
收藏
页码:54 / 61
页数:8
相关论文
共 50 条
[21]   Epigenetic modification of liver mitochondrial DNA is associated with histological severity of nonalcoholic fatty liver disease [J].
Jose Pirola, Carlos ;
Fernandez Gianotti, Tomas ;
Laura Burgueno, Adriana ;
Rey-Funes, Manuel ;
Fabian Loidl, Cesar ;
Mallardi, Pablo ;
San Martino, Julio ;
Osvaldo Castano, Gustavo ;
Sookoian, S. .
GUT, 2013, 62 (09) :1356-1363
[22]   Mitochondrial dysfunction, oxidative stress and apoptotic induction in microglial BV-2 cells treated with sodium arsenate [J].
Kharroubi, Wafa ;
Ahmed, Samia Haj ;
Nury, Thomas ;
Andreoletti, Pierre ;
Sakly, Rachid ;
Hammami, Mohamed ;
Lizard, Gerard .
JOURNAL OF ENVIRONMENTAL SCIENCES, 2017, 51 :44-51
[23]   Involvement of mtDNA Damage Elicited by Oxidative Stress in the Arsenical Skin Cancers [J].
Lee, Chih-Hung ;
Wu, Shi-Bei ;
Hong, Chien-Hui ;
Chen, Gwo-Shin ;
Wei, Yau-Huei ;
Yu, Hsin-Su .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2013, 133 (07) :1890-1900
[24]   Aberrant Cell Proliferation by Enhanced Mitochondrial Biogenesis via mtTFA in Arsenical Skin Cancers [J].
Lee, Chih-Hung ;
Wu, Shi-Bei ;
Hong, Chien-Hui ;
Liao, Wei-Ting ;
Wu, Ching-Ying ;
Chen, Gwo-Shing ;
Wei, Yau-Huei ;
Yu, Hsin-Su .
AMERICAN JOURNAL OF PATHOLOGY, 2011, 178 (05) :2066-2076
[25]   LCICP-MS Determinations of Unexposed UK Urinary Arsenic Speciation Reference Values [J].
Leese, Elizabeth ;
Morton, Jackie ;
Tan, Emma ;
Gardiner, Philip H. E. ;
Carolan, Vikki A. .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2014, 38 (01) :24-30
[26]  
Li J, 2010, PLOS GENET, V6
[27]  
Liu S. X, 2005, CANCER RES, V65, P8
[28]   Electrophile and oxidant damage of mitochondrial DNA leading to rapid evolution of homoplasmic mutations [J].
Mambo, E ;
Gao, XQ ;
Cohen, Y ;
Guo, ZM ;
Talalay, P ;
Sidransky, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (04) :1838-1843
[29]  
Martinez-Outschoom U. E, 2011, AM J PATHOL, V178
[30]  
Mawlood S. K, 2016, AGING, V8