Nuclear Research Center Negev, 84190, Beer-Sheba, Israel.
Ilse Katz Institute for Nanoscale Science and Technology, Ben Gurion University, Beer Sheba, Israel.
Cell Biochem Biophys. 2022 Dec;80(4):647-656. doi: 10.1007/s12013-022-01106-z. Epub 2022 Oct 11.
The dicentric chromosome assay (DCA), is considered the 'gold standard' for radiation biodosimetry. Yet, DCA, as currently implemented, may be impractical for emergency response applications, especially when time is of the essence, owing to its labor-intensive and time-consuming nature. The growth of a primary lymphocyte culture for 48 h in vitro is required for DCA, and manual scoring of dicentric chromosomes (DCs) requires an additional 24-48 h, resulting in an overall processing time of 72-96 h for dose estimation. In order to improve this timing. we introduce a protocol that will detect the metaphase cells in a population of cells, and then will harvest only those metaphase cells. Our metaphase enrichment approach is based on fixed human lymphocytes incubated with monoclonal, anti-phosphorylated H3 histone (ser 10). Antibodies against this histone have been shown to be specific for mitotic cells. Colcemid is used to arrest the mitotic cells in metaphase. Following that, a flow-cytometric sorting apparatus isolates the mitotic fraction from a large population of cells, in a few minutes. These mitotic cells are then spread onto a slide and treated with our C-Banding procedure [Gonen et al. 2022], to visualize the centromeres with DAPI. This reduces the chemical processing time to ~2 h. This reduces the time required for the DCA and makes it practical for a much wider set of applications, such as emergency response following exposure of a large population to ionizing radiation.
双着丝粒染色体分析(DCA)被认为是辐射生物剂量测定的“金标准”。然而,由于其劳动强度大且耗时的性质,目前实施的 DCA 可能不适用于应急响应应用,尤其是在时间紧迫的情况下。DCA 需要在体外培养原代淋巴细胞 48 小时,手动评分双着丝粒染色体(DC)需要另外 24-48 小时,因此剂量估计的总处理时间为 72-96 小时。为了改善这种情况,我们引入了一种方案,该方案可以检测细胞群体中的中期细胞,然后仅收获那些中期细胞。我们的中期富集方法基于与人淋巴细胞孵育的单克隆抗磷酸化 H3 组蛋白(丝氨酸 10)。已证明针对这种组蛋白的抗体特异性针对有丝分裂细胞。秋水仙素用于将有丝分裂细胞阻滞在中期。之后,流式细胞分选装置在几分钟内从大量细胞中分离出有丝分裂部分。然后将这些有丝分裂细胞铺在载玻片上,并使用我们的 C-带处理程序[Gonen 等人,2022 年]进行处理,用 DAPI 可视化着丝粒。这将化学处理时间缩短至~2 小时。这减少了 DCA 所需的时间,并使其更适用于更广泛的应用,例如大量人群暴露于电离辐射后的应急响应。