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转基因动物辐射防护中屏蔽材料影响的评估。

Evaluation of the impact of shielding materials in radiation protection in transgenic animals.

作者信息

Chang P Y, Doppalapudi Rupa, Bakke J, Puey A, Lin S

机构信息

SRI International, PN175, 333 Ravenswood Ave, Menlo Park, CA 94025, USA.

出版信息

Radiat Environ Biophys. 2007 Jun;46(2):113-8. doi: 10.1007/s00411-006-0074-z. Epub 2006 Nov 8.

DOI:10.1007/s00411-006-0074-z
PMID:17091306
Abstract

We are using a plasmid-based transgenic mouse mutation model system to evaluate the effectiveness of aluminum or low-density polyethylene (LDPE) shielding after 250 MeV/u protons or 1 GeV/u iron ion irradiation. Transgenic mice, with multiple copies of the plasmid pUR288 lacZ transgene integrated into the genome of every cell of the animal, were either irradiated or sham-treated. Multiple endpoints, including early cytogenetic damage in erythrocytes at 48 h after exposure, chromosome aberrations in bone marrow lymphocytes, and lacZ mutant frequencies (MF) in brain and spleen tissues were measured in the same animals. The frequency of total circulating reticulocytes (fRET) dropped precipitously at 48 h after 2 Gy of proton irradiation. The average level of micronucleated reticulocytes (fMN-RET) was fivefold higher in the irradiated samples relative to the controls at the same time point. There was an increase in total chromosome aberrations in bone marrow lymphocytes at 8 weeks after proton irradiation but this increase was not statistically significant relative to the controls. Evaluation of the lacZ MF in the brain and spleen tissues showed that proton irradiation induced a twofold increase in MF in each tissue. Similar samples were collected from animals that were shielded from the proton beam by aluminum. Compared to the unshielded treatment group, we noted no difference in fRET, fMN-RET, chromosome aberrations in lymphocytes and lacZ MF in brain and spleen tissues obtained from these animals. In a separate study, animals were exposed to high-energy iron ions with or without 10 or 15 cm LDPE. Using the same approach, we noted a precipitous drop in fRET, and an elevation in fMN-RET within 48 h after 1 Gy of iron ions. Total chromosome aberrations in bone marrow lymphocytes were slightly elevated but not significant at 8 weeks after iron ion exposure. Shielding animals with 10 or 15 cm of polyethylene appeared to have no effect on the level of RET, MN-RET or chromosome aberrations in these animals. LacZ MF in brain and spleen tissues increased 1.5-2-fold above control levels after 1 Gy iron ions at 8 weeks after treatment. On the other hand, MF in tissues harvested from shielded animals appeared to be lower than their unshielded litermates, suggesting the polyethylene shielding was effective in reducing the iron-induced genomic damage in tissues. Although shielding may be effective, in some cases, in reducing the physical dose of particle radiation, our cytogenetic results showed that the biological impact of the particle beam remain unchanged. On the other hand, reduction in transgene MF in tissues from LDPE-shielded animals but not in the aluminum-shielded animals strongly suggests that careful consideration of the biological endpoints used is necessary in the evaluation of the efficacy of the selected shielding material.

摘要

我们正在使用基于质粒的转基因小鼠突变模型系统,来评估在250 MeV/u质子或1 GeV/u铁离子辐照后铝或低密度聚乙烯(LDPE)屏蔽的有效性。将含有多个质粒pUR288 lacZ转基因拷贝且整合到动物每个细胞基因组中的转基因小鼠,进行辐照或假处理。在同一批动物中测量了多个终点指标,包括暴露后48小时红细胞中的早期细胞遗传学损伤、骨髓淋巴细胞中的染色体畸变,以及脑和脾组织中的lacZ突变频率(MF)。质子辐照2 Gy后48小时,总循环网织红细胞频率(fRET)急剧下降。在同一时间点,辐照样本中微核网织红细胞的平均水平(fMN-RET)相对于对照组高出五倍。质子辐照8周后,骨髓淋巴细胞中的总染色体畸变有所增加,但相对于对照组,这种增加没有统计学意义。对脑和脾组织中lacZ MF的评估表明,质子辐照使每个组织中的MF增加了两倍。从被铝屏蔽免受质子束照射的动物身上收集了类似的样本。与未屏蔽的治疗组相比,我们注意到这些动物的fRET、fMN-RET、淋巴细胞中的染色体畸变以及脑和脾组织中的lacZ MF没有差异。在另一项研究中,动物暴露于有或没有10或15厘米LDPE屏蔽的高能铁离子下。使用相同的方法,我们注意到铁离子辐照1 Gy后48小时内fRET急剧下降,fMN-RET升高。铁离子暴露8周后,骨髓淋巴细胞中的总染色体畸变略有升高,但不显著。用10或15厘米聚乙烯屏蔽动物似乎对这些动物的RET、MN-RET水平或染色体畸变没有影响。治疗8周后,1 Gy铁离子辐照使脑和脾组织中的lacZ MF比对照水平增加了1.5至2倍。另一方面,从屏蔽动物身上采集的组织中的MF似乎低于未屏蔽的同窝动物,这表明聚乙烯屏蔽在减少铁诱导的组织基因组损伤方面是有效的。尽管屏蔽在某些情况下可能有效地降低了粒子辐射的物理剂量,但我们的细胞遗传学结果表明粒子束的生物学影响保持不变。另一方面,LDPE屏蔽动物组织中的转基因MF降低,而铝屏蔽动物组织中的转基因MF未降低,这强烈表明在评估所选屏蔽材料的功效时,必须仔细考虑所使用的生物学终点指标。

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本文引用的文献

1
Shielding of relativistic protons.相对论质子的屏蔽
Radiat Environ Biophys. 2007 Jun;46(2):107-11. doi: 10.1007/s00411-006-0088-6. Epub 2007 Jan 26.
2
Cancer risk from exposure to galactic cosmic rays: implications for space exploration by human beings.暴露于银河宇宙射线的癌症风险:对人类太空探索的启示。
Lancet Oncol. 2006 May;7(5):431-5. doi: 10.1016/S1470-2045(06)70695-7.
3
Shielding and fragmentation studies.屏蔽与碎片化研究。
Radiat Prot Dosimetry. 2005;116(1-4 Pt 2):123-4. doi: 10.1093/rpd/nci064.
4
Cytogenetic effects of high-energy iron ions: dependence on shielding thickness and material.高能铁离子的细胞遗传学效应:对屏蔽厚度和材料的依赖性。
Radiat Res. 2005 Oct;164(4 Pt 2):571-6. doi: 10.1667/rr3362.1.
5
Proton-induced genetic damage in lacZ transgenic mice.
Radiat Res. 2005 Oct;164(4 Pt 2):481-6. doi: 10.1667/rr3322.1.
6
Implementation of ALARA radiation protection on the ISS through polyethylene shielding augmentation of the Service Module Crew Quarters.通过增加服务舱乘员舱的聚乙烯屏蔽,在国际空间站上实施尽可能低的合理可达到的辐射防护(ALARA)。
Adv Space Res. 2004;34(6):1333-7. doi: 10.1016/j.asr.2003.10.051.
7
Persistence of chromosome aberrations in mice acutely exposed to 56Fe+26 ions.急性暴露于56Fe+26离子的小鼠中染色体畸变的持续性
Radiat Res. 2004 Jun;161(6):648-55. doi: 10.1667/rr3177.
8
Long-term effects of low-dose proton radiation on immunity in mice: shielded vs. unshielded.低剂量质子辐射对小鼠免疫力的长期影响:屏蔽与非屏蔽情况
Aviat Space Environ Med. 2003 Feb;74(2):115-24.
9
HZE particle radiation induces tissue-specific and p53-dependent mutagenesis in transgenic animals.高能重粒子辐射在转基因动物中诱导组织特异性和p53依赖性诱变。
Phys Med. 2001;17 Suppl 1:189-91.
10
Dose and dose rate effects of whole-body proton irradiation on leukocyte populations and lymphoid organs: part I.全身质子照射对白细胞群体和淋巴器官的剂量及剂量率效应:第一部分
Immunol Lett. 2002 Jan 1;80(1):55-66. doi: 10.1016/s0165-2478(01)00306-6.