M'kacher Radhia, El Maalouf Elie, Terzoudi Georgia, Ricoul Michelle, Heidingsfelder Leonhard, Karachristou Ionna, Laplagne Eric, Hempel William M, Colicchio Bruno, Dieterlen Alain, Pantelias Gabriel, Sabatier Laure
Laboratoire de Radiobiologie et Oncologie, Commissariat à l'Energie Atomique, Fontenay-aux-Roses, France.
Laboratoire de Radiobiologie et Oncologie, Commissariat à l'Energie Atomique, Fontenay-aux-Roses, France; Laboratoire Modélisation Intelligence Processus Systèmes (MIPS)-Groupe TIIM3D, Université de Haute-Alsace, Mulhouse, France.
Int J Radiat Oncol Biol Phys. 2015 Mar 1;91(3):640-9. doi: 10.1016/j.ijrobp.2014.10.048. Epub 2015 Jan 14.
To combine telomere and centromere (TC) staining of premature chromosome condensation (PCC) fusions to identify dicentrics, centric rings, and acentric chromosomes, making possible the realization of a dose-response curve and automation of the process.
Blood samples from healthy donors were exposed to (60)Co irradiation at varying doses up to 8 Gy, followed by a repair period of 8 hours. Premature chromosome condensation fusions were carried out, and TC staining using peptide nucleic acid probes was performed. Chromosomal aberration (CA) scoring was carried out manually and automatically using PCC-TCScore software, developed in our laboratory.
We successfully optimized the hybridization conditions and image capture parameters, to increase the sensitivity and effectiveness of CA scoring. Dicentrics, centric rings, and acentric chromosomes were rapidly and accurately detected, leading to a linear-quadratic dose-response curve by manual scoring at up to 8 Gy. Using PCC-TCScore software for automatic scoring, we were able to detect 95% of dicentrics and centric rings.
The introduction of TC staining to the PCC fusion technique has made possible the rapid scoring of unstable CAs, including dicentrics, with a level of accuracy and ease not previously possible. This new approach can be used for biological dosimetry in radiation emergency medicine, where the rapid and accurate detection of dicentrics is a high priority using automated scoring. Because there is no culture time, this new approach can also be used for the follow-up of patients treated by genotoxic therapy, creating the possibility to perform the estimation of induced chromosomal aberrations immediately after the blood draw.
结合早前期染色体凝缩(PCC)融合的端粒和着丝粒(TC)染色来识别双着丝粒染色体、着丝粒环和无着丝粒染色体,从而实现剂量反应曲线的绘制以及该过程的自动化。
将来自健康供者的血样暴露于高达8 Gy的不同剂量的(60)Co辐射下,随后进行8小时的修复期。进行早前期染色体凝缩融合,并使用肽核酸探针进行TC染色。使用我们实验室开发的PCC-TCScore软件手动和自动进行染色体畸变(CA)评分。
我们成功优化了杂交条件和图像捕获参数,以提高CA评分的灵敏度和有效性。快速且准确地检测到了双着丝粒染色体、着丝粒环和无着丝粒染色体,通过手动评分在高达8 Gy时得到了线性二次剂量反应曲线。使用PCC-TCScore软件进行自动评分时,我们能够检测到95%的双着丝粒染色体和着丝粒环。
将TC染色引入PCC融合技术使得对包括双着丝粒染色体在内的不稳定染色体畸变进行快速评分成为可能,其准确性和便捷程度是以前无法达到的。这种新方法可用于放射应急医学中的生物剂量测定,在放射应急医学中,使用自动评分快速准确地检测双着丝粒染色体是高度优先事项。由于无需培养时间,这种新方法还可用于接受遗传毒性治疗患者的随访,使得在采血后立即进行诱导染色体畸变估计成为可能。