Prolonged expression of senescence markers in mice exposed to gamma-irradiation.
10.4142/jvs.2012.13.4.331
- Author:
Min A SEOL
1
;
Uhee JUNG
;
Hyeon Soo EOM
;
Seol Hwa KIM
;
Hae Ran PARK
;
Sung Kee JO
Author Information
1. Radiation Biotechnology Research Division, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup 580-185, Korea. uhjung@kaeri.re.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
mitochondrial DNA deletion;
p21;
radiation;
senescence;
senescence-associated beta-galactosidase
- MeSH:
Aging;
Animals;
Cell Aging;
DNA, Mitochondrial;
Female;
Humans;
Kidney;
Liver;
Lung;
Mice;
Radiation, Ionizing;
Radioactive Hazard Release;
Up-Regulation;
beta-Galactosidase
- From:Journal of Veterinary Science
2012;13(4):331-338
- CountryRepublic of Korea
- Language:English
-
Abstract:
Although ionizing radiation is known to induce cellular senescence in vitro and in vivo, its long-term in vivo effects are not well defined. In this study, we examined the prolonged expression of senescence markers in mice irradiated with single or fractionated doses. C57BL/6 female mice were exposed to 5 Gy of gamma-rays in single or 5, 10, 25 fractions. At 2, 4, and 6 months after irradiation, senescence markers including mitochondrial DNA (mtDNA) common deletion, p21, and senescence-associated beta-galactosidase (SA beta-gal) were monitored in the lung, liver, and kidney. Increases of mtDNA deletion were detected in the lung, liver, and kidney of irradiated groups. p21 expression and SA beta-gal staining were also increased in the irradiated groups compared to the non-irradiated control group. Increases of senescence markers persisted up to 6 months after irradiation. Additionally, the extent of mtDNA deletion and the numbers of SA beta-gal positive cells were greater as the number of radiation fractions increased. In conclusion, our results showed that ionizing radiation, especially that delivered in fractions, can cause the persistent upregulation of senescence marker expression in vivo. This should be considered when dealing with chronic normal tissue injuries caused by radiation therapy or radiation accidents.
