TY - JOUR
T1 - Monomethylarsonous acid
T2 - Induction of DNA damage and oxidative stress in mouse natural killer cells at environmentally-relevant concentrations
AU - Xu, Huan
AU - Wang, Xiaolei
AU - Wang, Wei
N1 - Funding Information:
This work was funded by a National Nature Science Foundation of China (grant No. 21738002 ). This work was also funded by a research grant from East China University of Science and Technology (grant No. YC 0142125 ).
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/8
Y1 - 2018/8
N2 - The carcinogenicity of arsenic has been confirmed in many studies, but its mechanism of action is still unclear. A lymphocyte component of the innate immune system, natural killer (NK) cells are responsible for killing cancer cells. Although inorganic arsenical species are the prevalent forms of arsenic in the environment, monomethylarsonous acid (MMA +3 ) is the major arsenical species found in immune-system cells, in this 30 d drinking-water-exposure study in mice. Therefore, the effect of MMA +3 on NK cells should be studied as a possible contributor to arsenic-induced toxicity at environmental exposure levels. In the mouse drinking-water-exposure model, As +3 induces dose-dependent DNA damage in NK cells. In in vitro studies, MMA +3 inhibited cell growth and induced DNA damage and oxidative stress at low concentration (20 and 50 nM) in isolated mouse NK cells. Strong correlations were found between DNA damage and oxidative stress in MMA +3 -treated mouse NK cells. Even at low concentrations relevant to environmental arsenic exposures, MMA +3 is genotoxic to primary mouse NK cells.
AB - The carcinogenicity of arsenic has been confirmed in many studies, but its mechanism of action is still unclear. A lymphocyte component of the innate immune system, natural killer (NK) cells are responsible for killing cancer cells. Although inorganic arsenical species are the prevalent forms of arsenic in the environment, monomethylarsonous acid (MMA +3 ) is the major arsenical species found in immune-system cells, in this 30 d drinking-water-exposure study in mice. Therefore, the effect of MMA +3 on NK cells should be studied as a possible contributor to arsenic-induced toxicity at environmental exposure levels. In the mouse drinking-water-exposure model, As +3 induces dose-dependent DNA damage in NK cells. In in vitro studies, MMA +3 inhibited cell growth and induced DNA damage and oxidative stress at low concentration (20 and 50 nM) in isolated mouse NK cells. Strong correlations were found between DNA damage and oxidative stress in MMA +3 -treated mouse NK cells. Even at low concentrations relevant to environmental arsenic exposures, MMA +3 is genotoxic to primary mouse NK cells.
KW - Arsenic
KW - Carcinogenesis
KW - Genotoxicity
KW - Monomethylarsonous acid
KW - Nature killer cells
KW - Oxidative stress
UR - http://www.scopus.com/inward/record.url?scp=85047618559&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85047618559&partnerID=8YFLogxK
U2 - 10.1016/j.mrgentox.2018.05.017
DO - 10.1016/j.mrgentox.2018.05.017
M3 - Article
C2 - 30057016
AN - SCOPUS:85047618559
SN - 1383-5718
VL - 832-833
SP - 1
EP - 6
JO - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
JF - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
ER -