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α 发射体镭-223 对离体血液内照射后白细胞中的 DNA 损伤。

DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223.

机构信息

Department of Nuclear Medicine, University of Würzburg, Oberdürrbacher Str. 6, 97080, Würzburg, Germany.

Bundeswehr Institute of Radiobiology affiliated to the University of Ulm, Neuherbergstr. 11, 80937, Munich, Germany.

出版信息

Sci Rep. 2018 Feb 2;8(1):2286. doi: 10.1038/s41598-018-20364-7.

Abstract

Irradiation with high linear energy transfer α-emitters, like the clinically used Ra-223 dichloride, severely damages cells and induces complex DNA damage including closely spaced double-strand breaks (DSBs). As the hematopoietic system is an organ-at-risk for the treatment, knowledge about Ra-223-induced DNA damage in blood leukocytes is highly desirable. Therefore, 36 blood samples from six healthy volunteers were exposed ex-vivo (in solution) to different concentrations of Ra-223. Absorbed doses to the blood were calculated assuming local energy deposition of all α- and β-particles of the decay, ranging from 0 to 142 mGy. γ-H2AX + 53BP1 co-staining and analysis was performed in leukocytes isolated from the irradiated blood samples. For DNA damage quantification, leukocyte samples were screened for occurrence of α-induced DNA damage tracks and small γ-H2AX + 53BP1 DSB foci. This revealed a linear relationship between the frequency of α-induced γ-H2AX damage tracks and the absorbed dose to the blood, while the frequency of small γ-H2AX + 53BP1 DSB foci indicative of β-irradiation was similar to baseline values, being in agreement with a negligible β-contribution (3.7%) to the total absorbed dose to the blood. Our calibration curve will contribute to the biodosimetry of Ra-223-treated patients and early after incorporation of α-emitters.

摘要

用高线性能量转移的 α 放射源辐照,如临床使用的镭-223 二氯化物,会严重损伤细胞,并诱导复杂的 DNA 损伤,包括紧密间隔的双链断裂(DSB)。由于造血系统是治疗的靶器官,因此非常需要了解镭-223 在血液白细胞中引起的 DNA 损伤。因此,从 6 名健康志愿者中采集了 36 份血液样本,在体外(溶液中)暴露于不同浓度的镭-223 下。假设衰变的所有 α 和 β 粒子的局部能量沉积,计算血液的吸收剂量,范围从 0 到 142 mGy。对从辐照血液样本中分离出的白细胞进行 γ-H2AX+53BP1 共染色和分析。为了进行 DNA 损伤定量,对白细胞样本进行了 α 诱导的 DNA 损伤轨迹和小 γ-H2AX+53BP1 DSB 焦点的筛查。这揭示了α 诱导的 γ-H2AX 损伤轨迹的频率与血液吸收剂量之间的线性关系,而指示 β 辐照的小 γ-H2AX+53BP1 DSB 焦点的频率与基线值相似,这与β 对血液总吸收剂量的贡献可忽略(3.7%)一致。我们的校准曲线将有助于镭-223 治疗患者的生物剂量测定和 α 发射器掺入后的早期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/5797089/5dd7b86ebcd3/41598_2018_20364_Fig1_HTML.jpg

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