Diesel exhaust particles cause increased levels of DNA deletions after transplacental exposure in mice

被引:33
|
作者
Reliene, R
Hlavacova, A
Mahadevan, B
Baird, WM
Schiestl, RH
机构
[1] Univ Calif Los Angeles, Geffen Sch Med, Dept Pathol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Geffen Sch Med, Dept Environm Hlth, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Geffen Sch Med, Dept Radiat Oncol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Sch Publ Hlth, Los Angeles, CA 90024 USA
[5] Oregon State Univ, Dept Environm & Mol Toxicol, Corvallis, OR 97331 USA
关键词
diesel exhaust particles; mouse; DNA adducts; DNA deletions; p(un) reversions;
D O I
10.1016/j.mrfmmm.2004.11.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Diesel exhaust particles (DEP) are a major source of air-borne pollution and are linked to increased risk of disease including lung cancer. Here we investigated effects of exposure to DEP on the frequency of DNA deletions, levels of oxidative DNA damage and DNA adduct formation during embryonic development in mice. Pregnant dams were orally exposed to various doses of DEP (500, 250, 125, 62.5, 31.25 mg/kg/day) at embryonic days 10.5-15.5. We determined the frequency of 70 kb DNA deletions spanning exons 6-18 at the p(un) allele that results in black-pigmented spots in the unpigmented retinal pigment epithelium in the eyes of p(un)/p(un) offspring mice. DEP caused a significant increase in the frequency of DNA deletions. Levels of 8-OH deoxyguanosine indicating oxidative DNA damage were within the limits of the unexposed mouse embryos. P-33 post-labeling analysis revealed very low levels of DNA adducts in the embryo tissue. Thus, transplacental exposure to DEP resulted in a significant increase in the frequency of DNA deletions in the mouse fetus and such genetic alterations in the offspring may have pathological consequences later in life. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 252
页数:8
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