An efficient and simple method for enriching metaphase cells for dicentric chromosome assay

被引:0
|
作者
Nakayama, Ryo [1 ]
Tran, Thanh-Mai [1 ,2 ]
Anderson, Donovan [1 ]
Takebayashi, Kai [1 ]
Goh, Valerie Swee Ting [3 ]
Fujishima, Yohei [1 ]
Miura, Tomisato [1 ]
机构
[1] Hirosaki Univ, Inst Radiat Emergency Med, Dept Risk Anal & Biodosimetry, 66-1 Hon Cho, Hirosaki 0368564, Japan
[2] Nucl Res Inst, Ctr Radiat Technol & Biotechnol, 1 Nguyen Tu Luc,Ward 8, Dalat City 67000, Lamdong, Vietnam
[3] Natl Univ Singapore, Dept Radiobiol, Singapore Nucl Res & Safety Initiat, 1 Create Way, Singapore 138602, Singapore
关键词
D O I
10.1093/rpd/ncae048
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
As compared to peripheral blood mononuclear cell (PBMC) culture, a lower mitotic index (MI) is seen in whole blood (WB) culture, but WB can be directly used for culture in dicentric chromosome assay (DCA). The purpose of this study is to develop a simple protocol for metaphase enrichment to improve the metaphase frequency of WB culture. Fixed cells were obtained after performing WB and PBMC cultures for DCA after conventional fixation. An additional low-speed centrifugation of 200 x g for 1 min was performed, separating the fixed cells of WB culture into a pellet and a supernatant fraction. The additional low-speed centrifugation enriched metaphase frequency and provided an MI comparable to the PBMC culture in the pellet fraction. Our study suggests that it is possible to increase the number of metaphase cells on slides using the slow centrifugation method, which could contribute to the efficiency of chromosome aberration analysis in biodosimetry.
引用
收藏
页码:1641 / 1646
页数:6
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