TY - JOUR
T1 - Environmental radiation on large Japanese field mice in Fukushima reduced colony forming potential in hematopoietic progenitor cells without inducing genomic instability
AU - Ariyoshi, Kentaro
AU - Miura, Tomisato
AU - Kasai, Kosuke
AU - Goh, Valerie Swee Ting
AU - Fujishima, Yohei
AU - Nakata, Akifumi
AU - Takahashi, Atsushi
AU - Shimizu, Yoshinaka
AU - Shinoda, Hisashi
AU - Yamashiro, Hideaki
AU - Seymour, Colin
AU - Mothersill, Carmel
AU - Yoshida, Mitsuaki A.
N1 - Funding Information:
This work was supported in part by the Japan Society for the Promotion of Science Grant-in-Aid for Scientific Research (C) [19K12354]. The authors express their deep appreciation of Namie Town’s local government in Fukushima Prefecture, Japan. The authors thank the laboratory staff for technical and secretarial assistance. The authors would also like to thank Editage (www.editage.jp) for English language editing.
Publisher Copyright:
© Copyright © 2020 Taylor & Francis Group LLC.
PY - 2022
Y1 - 2022
N2 - Purpose: To study the environmental radiation effects of wild animals after the Fukushima Dai-ichi nuclear power plant accident, we assessed effects on hematopoietic progenitor cells (HPCs) in large Japanese field mice (Apodemus speciosus). Materials and methods: A. speciosus were collected from three contaminated sites and control area. The air dose-rates at the control and contaminated areas were 0.96 ± 0.05 μGy/d (Hirosaki), 14.4 ± 2.4 μGy/d (Tanashio), 208.8 ± 31.2 μGy/d (Ide), 470.4 ± 93.6 μGy/d (Omaru), respectively. We investigated possible DNA damage and pro-inflammatory markers in the bone marrow (BM) cells. The colony-forming potential of BM cells was estimated by the number of HPC colony-forming cells. Radiation-induced genomic instability (RIGI) in HPCs was also analyzed by quantifying delayed DNA damage in CFU-GM clones. Results: Although no significant differences in DNA damage and inflammation markers in BM cells from control and contaminated areas, the number of HPC colonies exhibited an inverse correlation with air dose-rate. With regard to RIGI, no significant differences in DNA damage of CFU-GM clones between the mice from the control and the three contaminated areas. Conclusions: Our study suggests that low dose-rate radiation of more than 200 Gy/d reduced HPCs, possibly eliminating genomically unstable HPCs.
AB - Purpose: To study the environmental radiation effects of wild animals after the Fukushima Dai-ichi nuclear power plant accident, we assessed effects on hematopoietic progenitor cells (HPCs) in large Japanese field mice (Apodemus speciosus). Materials and methods: A. speciosus were collected from three contaminated sites and control area. The air dose-rates at the control and contaminated areas were 0.96 ± 0.05 μGy/d (Hirosaki), 14.4 ± 2.4 μGy/d (Tanashio), 208.8 ± 31.2 μGy/d (Ide), 470.4 ± 93.6 μGy/d (Omaru), respectively. We investigated possible DNA damage and pro-inflammatory markers in the bone marrow (BM) cells. The colony-forming potential of BM cells was estimated by the number of HPC colony-forming cells. Radiation-induced genomic instability (RIGI) in HPCs was also analyzed by quantifying delayed DNA damage in CFU-GM clones. Results: Although no significant differences in DNA damage and inflammation markers in BM cells from control and contaminated areas, the number of HPC colonies exhibited an inverse correlation with air dose-rate. With regard to RIGI, no significant differences in DNA damage of CFU-GM clones between the mice from the control and the three contaminated areas. Conclusions: Our study suggests that low dose-rate radiation of more than 200 Gy/d reduced HPCs, possibly eliminating genomically unstable HPCs.
KW - Apodemus speciosus
KW - Radiation effect
KW - hematopoietic progenitor cells
KW - radiation-induced genomic instability
KW - wild animal
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U2 - 10.1080/09553002.2020.1807643
DO - 10.1080/09553002.2020.1807643
M3 - Article
C2 - 32791031
AN - SCOPUS:85089661791
SN - 0955-3002
VL - 98
SP - 1147
EP - 1158
JO - International Journal of Radiation Biology
JF - International Journal of Radiation Biology
IS - 6
ER -