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外周血淋巴细胞作为评估低剂量辐射所致基因组不稳定性的体外模型

Peripheral Blood Lymphocytes as In Vitro Model to Evaluate Genomic Instability Caused by Low Dose Radiation.

作者信息

Tewari Shikha, Khan Kainat, Husain Nuzhat, Rastogi Madhup, Mishra Surendra P, Srivastav Anoop K

机构信息

Pathology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India E-mail :

出版信息

Asian Pac J Cancer Prev. 2016;17(4):1773-7. doi: 10.7314/apjcp.2016.17.4.1773.

Abstract

Diagnostic and therapeutic radiation fields are planned so as to reduce side-effects while maximising the dose to site but effects on healthy tissues are inevitable. Radiation causes strand breaks in DNA of exposed cells which can lead to chromosomal aberrations and cause malfunction and cell death. Several researchers have highlighted the damaging effects of high dose radiation but still there is a lacuna in identifying damage due to low dose radiation used for diagnostic purposes. Blood is an easy resource to study genotoxicity and to estimate the effects of radiation. The micronucleus assay and chromosomal aberration can indicate genetic damage and our present aim was to establish these with lymphocytes in an in vitro model to predict the immediate effects low dose radiation. Blood was collected from healthy individuals and divided into 6 groups with increasing radiation dose i.e., 0Gy, 0.10Gy, 0.25Gy, 0.50Gy, 1Gy and 2Gy. The samples were irradiated in duplicates using a LINAC in the radiation oncology department. Standard protocols were applied for chromosomal aberration and micronucleus assays. Metaphases were stained in Giemsa and 200 were scored per sample for the detection of dicentric or acentric forms. For micronuclei detection, 200 metaphases. Giemsa stained binucleate cells per sample were analysed for any abnormality. The micronuclei (MN) frequency was increased in cells exposed to the entire range of doses (0.1- 2Gy) delivered. Controls showed minimal MN formation (2.0%±0.05) with triple MN (5.6%±2.0) frequency at the lowest dose. MN formation increased exponentially with the radiation dose thereafter with a maximum at 2Gy. Significantly elevated numbers of dicentric chromosomes were also observed, even at doses of 0.1- 0.5Gy, compared to controls, and acentric chromosomes were apparent at 2Gy. In conclusion we can state that lymphocytes can be effectively used to study direct effect of low dose radiation.

摘要

诊断和治疗性辐射野的规划旨在减少副作用,同时使靶部位的剂量最大化,但对健康组织的影响不可避免。辐射会导致受照射细胞的DNA链断裂,这可能导致染色体畸变,并引起功能异常和细胞死亡。几位研究人员强调了高剂量辐射的破坏作用,但在确定用于诊断目的的低剂量辐射造成的损害方面仍存在空白。血液是研究遗传毒性和评估辐射影响的便捷资源。微核试验和染色体畸变可以表明遗传损伤,我们目前的目标是在体外模型中用淋巴细胞建立这些指标,以预测低剂量辐射的即时影响。从健康个体采集血液,分为6组,辐射剂量递增,即0Gy、0.10Gy、0.25Gy、0.50Gy、1Gy和2Gy。样本在放射肿瘤学部门使用直线加速器进行一式两份照射。染色体畸变和微核试验采用标准方案。中期相用吉姆萨染色,每个样本计数200个中期相以检测双着丝粒或无着丝粒形式。对于微核检测,每个样本分析200个吉姆萨染色的双核细胞有无异常。在接受整个剂量范围(0.1 - 2Gy)照射的细胞中,微核(MN)频率增加。对照组在最低剂量时微核形成最少(2.0%±0.05),三微核频率为(5.6%±2.0)。此后,微核形成随辐射剂量呈指数增加,在2Gy时达到最大值。与对照组相比,即使在0.1 - 0.5Gy剂量下也观察到双着丝粒染色体数量显著增加,在2Gy时无着丝粒染色体明显可见。总之,我们可以说淋巴细胞可有效地用于研究低剂量辐射的直接影响。

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