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基于 FISH 的 G2-PCC 检测在高辐射剂量暴露的细胞遗传学评估中的应用:对快速分类生物剂量学的潜在影响。

Application of FISH based G2-PCC assay for the cytogenetic assessment of high radiation dose exposures: Potential implications for rapid triage biodosimetry.

机构信息

Cytogenetic Biodosimetry Laboratory, Radiation Emergency Assistance Center/Training Site, Oak Ridge Institute for Science and Education, Oak Ridge Associated Universities, Oak Ridge, Tennessee, United States of America.

Center for Radiological Research, Department of Radiation Oncology, Columbia University Medical Center, New York, New York, United States of America.

出版信息

PLoS One. 2024 Oct 25;19(10):e0312564. doi: 10.1371/journal.pone.0312564. eCollection 2024.

Abstract

The main goal of this study is to test the utility of calyculin A induced G2-PCC assay as a biodosimetry triage tool for assessing a wide range of low and acute high radiation dose exposures of photons. Towards this initiative, chromosome aberrations induced by low and high doses of x-rays were evaluated and characterized in G2-prematurely condensed chromosomes (G2-PCCs) by fluorescence in situ hybridization (FISH) using human centromere and telomere specific PNA (peptide nucleic acid) probes. A dose dependent increase in the frequency of dicentric chromosomes was observed in the G2-PCCs up to 20 Gy of x-rays. The combined yields of dicentrics and rings in the G2-PCCs showed a clear dose dependency up to 20 Gy from 0.02/cell for 0.1 Gy to 14.98/cell for 20 Gy. Centric rings were observed more frequently than acentric ring chromosomes in the G2-PCCs at all the radiation doses from 1 Gy to 20 Gy. A head-to-head comparison was also performed by FISH on the yields of chromosome aberrations induced by different doses of x-rays (0 Gy -7.5 Gy) in colcemid arrested metaphase chromosomes and calyculin A induced G2-PCCs. In general, the frequencies of dicentrics, rings and acentric fragments were slightly higher in G2-PCCs than in colcemid arrested metaphase chromosomes at all the radiation doses, but the differences were not statistically significant. To reduce the turnaround time for absorbed radiation dose estimation, attempt was made to obtain G2-PCCs by reducing the culture time to 36 hrs. The absorbed doses estimated in x-rays irradiated (0,1,2 and 4 Gy) G2-PCCs after 36 hrs of culture were grossly like that of G2-PCCs and colcemid arrested metaphase chromosomes prepared after 48 hrs of culture. Our study indicates that the shortened version of calyculin A induced G2-PCC assay coupled with the FISH staining technique can serve as an effective triage biodosimetry tool for large-scale radiological/nuclear incidents.

摘要

本研究的主要目的是测试钙调神经磷酸酶诱导的 G2-PCC 检测作为评估光子低剂量和急性高剂量照射的生物剂量学筛选工具的效用。为此,我们通过荧光原位杂交(FISH)技术,用人类着丝粒和端粒特异性 PNA(肽核酸)探针,评估和分析了低剂量和高剂量 X 射线诱导的 G2-早熟凝聚染色体(G2-PCC)中的染色体畸变。在 G2-PCC 中,双着丝粒染色体的频率随着 X 射线剂量的增加而增加,最高可达 20Gy。在 G2-PCC 中,双着丝粒和环的联合产量在 0.02/cell(0.1Gy)至 14.98/cell(20Gy)之间呈现出明显的剂量依赖性。在所有 1Gy 至 20Gy 的辐射剂量下,G2-PCC 中的着丝粒环染色体比无着丝粒环染色体更为常见。我们还通过 FISH 对头对头比较了不同剂量 X 射线(0Gy-7.5Gy)在秋水仙素阻断中期染色体和钙调神经磷酸酶诱导的 G2-PCC 中诱导的染色体畸变产量。总的来说,在所有辐射剂量下,G2-PCC 中的双着丝粒、环和无着丝粒片段的频率略高于秋水仙素阻断中期染色体,但差异无统计学意义。为了减少吸收剂量估算的周转时间,我们尝试通过将培养时间缩短至 36 小时来获得 G2-PCC。在培养 36 小时后,用 X 射线照射(0、1、2 和 4Gy)的 G2-PCC 估算的吸收剂量与培养 48 小时后获得的 G2-PCC 和秋水仙素阻断中期染色体的吸收剂量大致相同。我们的研究表明,钙调神经磷酸酶诱导的 G2-PCC 检测的缩短版本与 FISH 染色技术相结合,可以作为大规模放射/核事件的有效筛选生物剂量学工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7f/11508073/509222223b7d/pone.0312564.g001.jpg

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