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

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 × 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.

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Publication Details

Journal
Radiation Protection Dosimetry
Published
2024-11-01
DOI
https://doi.org/10.1093/rpd/ncae048
Citations
2
Primary Topic
Molecular Biology Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.47
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article

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

Yohei Fujishima, Kai Takebayashi, Valerie Swee Ting Goh, R Nakayama et al.
2 citations
Radiation Protection Dosimetry
Molecular Biology Techniques and Applications
0.47
article

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

Yohei Fujishima, Kai Takebayashi, Valerie Swee Ting Goh, R Nakayama, Donovan Anderson, Tomisato Miura, Thi My Hien Tran
article en
2 citations

Abstract

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 × 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.

Radiation Protection DosimetryVol. 200(16-18)
Hirosaki University (JP), National University of Singapore (SG), Dalat University (VN)
Openalex Percentile: Top 34%
Molecular Biology Techniques and Applications
0.47
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