C离子辐照引起细胞分泌旁效应信号因子浓度随时间的变化

信号因子通常能介导旁效应的发生。 利用高LET C离子辐照体外培养的人肝癌QGY-7703细胞, 检测辐照后不同时刻培养基中信号因子TGF-β1和NO的浓度, 并通过转移培养基法检测照射后不同时刻转移培养基对人肝L02旁细胞存活率和代谢活力的影响, 发现受照射细胞在时间与空间上调控着周围信号因子的浓度, 并且通过信号因子浓度的变化影响旁细胞的各种效应发生。 实验为旁效应的解释提供了新的实验数据。 Signaling factors usually play an important role in bystander effect. In this work, human hepatoma QGY 7703 cells in vitro were irradiated with high LET carbon ions. Concentrations of signaling factors such as TGF-β1 and NO were measured in the media of the irradiated QGY-7703 cells at different time points after irradiation. The conditioned media harvested at various times post irradiation were transferred to human hepatocyte L02 cells as bystander cells and then the influence of the conditioned media on survival fraction and cell viability of the bystander cells were determined. The results show that the irradiated cells regulate the concentration of the signaling factors released nearby themselves temporally and spatially, and the bystander cells response to the signaling factors differentially according to the concentration change. This work provides new basic data for exploring the bystander effect, especially caused by high LET radiation.     

辐射诱发体内旁效应特征的研究进展

大量的细胞生物学研究显示, 辐射诱发旁效应的传输信号包括活性氧自由基（ROS）、 一氧化氮自由基（NO）以及一些细胞因子。 近年来,越来越多的文献报道关于体内旁效应特征的研究, 并已经证实在生物体内辐射诱导的旁效应不仅能发生在相邻组织, 还可发生在远源器官。这些体内旁效应包括DNA损伤、表观遗传学改变、miRNA及基因表达改变、 细胞增殖和凋亡等。 为了总结和分析辐射诱发体内旁效应的特征, 本文综述了辐射诱发体内旁效应的特点, 包括其与性别、 传播途径、辐射品质的关系以及相关机制的研究。 Radiation induced bystander effect is defined as the induction of damage in neighboring non hit cells by signals released from directly irradiated cells. ROS, NO and cytokines are involved in signaling pathways of bystander effects. Recently, the bystander effects in vivo have been reported more and more. It has been indicated that radiation induced bystander effect was localized not only in bystander tissues but also in distant organs. This effect includes many biological endpoints such as DNA damage, epigenetic, miRNA and gene expression changes, cell proliferation and apoptosis. In this review we described different aspects of ionizing radiation induced bystander effects such as its characteristics, sex specific, signaling transfer, dose and LET dependence, and related mechanisms.     

电离辐射诱导的旁观者效应研究

列举了一些具有代表性的研究结果， 概括介绍了一些产生旁观者效应的可能机制以及辐照引起的活性氧基团或分子、 细胞通讯和细胞因子在旁观者效应中的重要作用. 此外， 还讨论了旁观者效应的表达程度与辐照剂量和射线品质的关系. 旁观者效应的研究结果表明: 辐射产生的潜在危害可能要比以前估计的大， 这给如何评估辐射对人类造成的危害带来了新的冲击. Recent studies have indicated that biological effects, such as chromosomal aberration, gene mutation and cell death and so on, can be induced in cells that are not traversed by radiation directly. This phenomenon has been termed as bystander effects. In this paper, a few representative studies were reported and the possible mechanisms underlying the bystander effects were summarized. The reactive oxygen species (ROS) induced by ionizing radiation, cellular communication and some factors play important roles. Besides, the expression extent of bystander effects depended on radiation dose and quality were discussed. Bystander effects suggest that potential health risks associated with radiation exposure may be greater than those of original thought and this makes ultimate impact on human radiation risk assessment.     

内质网应激对碳离子辐照宫颈癌HeLa 细胞的影响

利用不同剂量的碳离子辐照二硫苏糖醇(2.5 mmol/L) 预处理的HeLa 细胞,探讨了内质网应激反应对碳离子辐照宫颈癌HeLa 细胞的影响。实验发现:与单独辐照组相比,二硫苏糖醇联合碳离子辐照后细胞的存活率下降,而凋亡率增加;二硫苏糖醇联合碳离子辐照加重了碳离子辐照引起的细胞周期阻滞;且联合辐照组的自噬被明显激活。结果表明,持续的内质网应激可改变宫颈癌HeLa 细胞对碳离子辐照反应,且二硫苏糖醇可能通过影响HeLa 细胞的自噬性细胞死亡通路发挥作用。To investigate the effect of endoplasmic reticulum stress on HeLa cells to 12C6+ ion irradiation,HeLa cells were pretreated with 2.5 mmol/L dithiothreitol and irradiated by 12C6+ ions with different doses.The results showed that, compared with IR alone, dithiothreitol combined with carbon ion irradiation caused HeLa cell survival decreased, and the apoptosis increased. Moreover, dithiothreitol and carbon ion radiation combination treatment led to a significant increase of G2/M phase, and autophagy was activated obviously in combination treatment group. The results imply that continuous endoplasmic reticulum stress can change the response of HeLa cells to 12C6+ irradiation, and dithiothreitol may affect HeLa cells through the autophagy cell death pathway.     

辐照诱导人正常肝细胞系HL-7702 细胞远后的微卫星不稳定性

采用高传能线密度(LET) 的12C6+离子束和低LET 的X 射线辐照人正常肝细胞系HL-7702 细胞,利用微卫星不稳定性(MSI) 检测来分析直接受照射细胞和通过转移培养基方式旁细胞传代八代子细胞以MSI 表征的远后效应。实验结果表明,12C6+离子束诱导的远后效应较X射线的低;旁细胞的远后效应较直接受照射细胞的高;辐射引起的MSI 与杂合性丢失(LOH) 的发生率具有位点特异性。结果提示,重离子放射治疗较X 射线放射治疗对正常组织引发的辐射风险要小,可通过对MSI 高发位点的筛选来评估放疗后患者长期生存状况和二次癌症发生风险。Human normal liver cell line HL-7702 cells were irradiated with high linear energy transfer (LET) 12C6+ ions and low-LET X-rays, respectively. Delayed effect in terms of microsatellite instability (MSI) in progenies of the directly irradiated cells and bystander cells, obtained in the way of medium transfer at the 8th passage postirradiation,were examined. The delayed effect induced by the high-LET 12C6+ ions was different from that induced by the low-LET X-rays, and a higher incidence of MSI was observed in the progenies of the cells after exposure to the X-rays than to the 12C6+ ions. We also found that the delayed effect in the progenies of the bystander cells was much more severe than thoseof directly irradiated cells. Furthermore, the events of MSI and loss of heterozygosity (LOH) induced by the ionizing radiations were not randomly distributed throughout the genome and specific loci existed indeed. These results imply that the radiation risk to normal tissues is lower in heavy ion therapy than in conventional X-ray radiotherapy, and the analysis of microsatellite loci with MSI high frequency occurrence can be applied to access long-term survival condition and second cancer risk for the patients after radiotherapy.     

羧甲基-β-1,3-葡聚糖对人肝癌HepG2细胞的放射增敏作用

本研究旨在探讨羧甲基-β-1,3葡聚糖（CMG）对人肝癌HepG2细胞X射线或12C6+离子束辐射敏感性的影响。首先用CCK-8法检测CMG对HepG2细胞的生长抑制情况,得到半数抑制浓度（IC50）为120.6μg/mL。用浓度为0.1×IC50的CMG预处理HepG2细胞24 h,再给予2 Gy X射线或12C6+离子束辐照（CMG+辐照组）;CMG未处理组直接接受2 Gy X射线或12C6+离子束辐照（辐照组）。对比分析辐照组和CMG+辐照组细胞的克隆存活、DNA损伤、凋亡与周期分布、细胞内活性氧（ROS）水平。发现:与X射线辐照组相比,相同剂量的12C6+离子辐照组克隆存活率更小,DNA损伤和周期阻滞更加严重,细胞凋亡率和细胞内ROS水平也更高。与单独X射线或12C6+离子束辐照组相比,CMG+辐照组克隆存活率明显降低,细胞凋亡率随辐照后CMG作用时间的延长而明显增加,CMG使辐照后细胞内ROS维持在一个较高的水平,同时CMG明显加重了单独辐照诱导的DNA损伤和周期阻滞。结果表明,与X射线相比,HepG2细胞对相同剂量的12C6+离子辐射更敏感;CMG可增加HepG2细胞对X射线或12C6+离子辐射的敏感性;CMG可能通过增加受照HepG2细胞内的ROS水平,加剧辐照诱导的DNA损伤,促进辐射诱导细胞凋亡而起到辐射增敏作用。This study aims to investigate the effect of carboxymethy-β-1, 3-glucan (CMG) on the sensitivity of human hepatoma HepG2 cells to X-rays or 12C6+ ions irradiation. First, the inhibitory effect of CMG on the growth of HepG2 cells was detected by CCK-8 assay, and the half maximal inhibitory concentration (IC50) was 120.6 μg/mL. HepG2 cells were pretreated with CMG at a concentration of 0.1×IC50 for 24 h and then irradiated with 2 Gy X-ray or 12C6+ ion beams (CMG + irradiation group). CMG untreated group was directly irradiated by 2 Gy X-rays or 12C6+ ions beam (irradiation group). The clone survival, DNA damage, cell apoptosis, cell cycle distribution, and intracellular reactive oxygen species (ROS) levels in irradiation group and CMG + irradiation group were comparatively analyzed. The results showed that the clone survival rate was lower, DNA damage and cycle arrest were more serious, and the rate of apoptosis and intracellular ROS levels were higher in 12C6+ ions irradiation group than those in the same dose of X-rays irradiation group. Compared with X-rays or 12C6+ ions irradiation group, the clone survival rate of CMG + irradiation group was significantly decreased, and the apoptosis rate significantly increased with the prolongation of CMG treatment post-irradiation; CMG maintained intracellular ROS at a higher level after irradiation, CMG also significantly aggravated radiation-induced DNA damage and cycle arrest. These results indicated that HepG2 cells were more sensitive to 12C6+ ions radiation than those at the same dose of X-rays. CMG increased the sensitivity of HepG2 cells to X-rays or 12C6+ ions irradiation by increasing intracellular ROS level, exacerbating radiation-induced DNA damage and promoting radiation-induced apoptosis in irradiated HepG2 cells.     

3D组织培养模型及其在辐射诱导旁效应研究中的应用

综述了3D细胞培养技术（TDCC）的发展, 3种主要的体外组织构建方法; 辐射诱导2D细胞产生旁效应的现象与机理; 人工构建的3D组织辐射后诱导的旁效应及其细胞间信号传导机理。 重离子（C离子）辐照作为一种重要的放疗工具, 对其辐射处理3D组织后诱导产生的旁效应进行了展望。 由于3D组织更接近人体细胞生长的真实环境, 因而以3D组织作为模型研究辐射诱导的旁效应, 对于辐射旁效应的防护和治疗可能具有重要的指导意义。 Compared with the cultured monolayer (2D) cells, three dimensional (3D) tissue could be more similar to the environment in vivo including the physical support, chemical factors, cell cell and cell matrix interaction and so on. With the development of three dimensional cell culture techniques (TDCC), 3D tissue is widely used in the areas of bystander effect research. This review focuses on introducing the TDCC method and its application in bystander effect research. First, the development process of 3D tissue culture method was introduced. Secondly, the induction of radiation induced bystander effects both in 2D cell and 3D tissue and its mechanisms were reviewed. Finally, because heavy ion (carbon ion beam) has been developed as a useful tool to cure solid cancer ,and the 3D tissue model is an ideal material to study the damages on body after being irradiated and to understand the underlying mechanisms, future study about heavy ion radiation inducing bystander effect in 3D tissue was discussed.     

辐照诱导的人正常肝细胞系HL-7702细胞延迟效应

利用X射线辐照人正常肝细胞系HL-7702细胞, 运用胞质分离阻滞微核法实验检测细胞微核率,AnnexinV FITC细胞凋亡检测试剂盒检测细胞凋亡率, 细胞微核率和凋亡率随着辐照剂量的增加而显著增加。X射线照射后细胞传代培养, 第7代时不同剂量辐照后子代细胞微核率和凋亡率同未辐照细胞相比已无明显区别。 对不同剂量辐照后传代7代的细胞再次照射2.5 Gy的相同剂量,发现它们细胞微核率和凋亡率存在明显差异,即初次受辐照剂量高的细胞, 再次以相同剂量辐照后的微核率和凋亡率也高. 这些结果表明,X射线辐照导致了HL-7702细胞基因组不稳定性这一辐射延迟效应,再次辐照使得辐射的延迟效应得以明显的表现。 Human normal liver cell line HL-7702 cells were irradiated with different doses of X rays. Micronucleus and apoptosis rates in the irradiated cells were measured with cytokinesis block micronucleus method and Annexin V FITC apoptosis detection kit, respectively. Experimental data showed that the micronucleus and apoptosis rates increased obviously with increasing irradiation dose. After seven population doublings, the micronucleus and apoptosis rates of the cells surviving exposure to the X rays reduced to the same levels as non irradiated control cells; the progenies of the cells were secondly exposed to X rays at the same dose of 2.5 Gy. We found that the progenies of the cells surviving the first irradiations of the various doses showed markedly differential micronucleus frequencies and apoptotic rates. Although the same dose of 2.5 Gy was applied in the second irradiations, the micronucleus frequencies and apoptotic rates of the progenies of the cells initially exposed at higher doses were significantly higher than the others. These results indicate that X rays lead to genomic instability in HL 7702 cells, which is an important manifestation of radiation induced delayed effect, and a second radiation stimulus makes the delayed effect in the progeny of the previously irradiated cells be expressed obviously.     

X射线致HeLa细胞损伤过程中NADPH氧化酶的作用

以HeLa细胞为实验材料, 探讨了NADPH氧化酶在X射线诱导细胞损伤过程中的作用。 结果显示, 12 Gy X射线辐照后细胞内活性氧(ROS)明显增加, 在用NADPH氧化酶抑制剂处理后再辐照, 则细胞内ROS降低到未辐照水平; 同时辐照后NADPH 氧化酶细胞质亚基p47phox 在细胞质积聚并和细胞膜亚基 gp91phox 结合; Western blotting检测结果显示, NADPH 氧化酶的关键亚基 gp91phox 的表达量明显增加。 以上结果说明, NADPH氧化酶可以被X射线激活, 由其介导产生的ROS在X射线诱导HeLa细胞损伤过程中扮演重要角色。 To investigate the role of NADPH oxidase in HeLa cell lesion induced by X ray irradiation, the change of cell survival was detected with MTT assay, reactive oxygen species (ROS) was measured by fluorospectrophotometer. Immunostaining and confocal laser scanning microscopy was employed to detect the co localization of two subunit of NADPH oxidase, p47phox and gp91phox in the cell. Western blotting was used to detect the expression of gp91phox before and after X ray irradiation. After X ray irradiation, intra cellular level of ROS increased obviously. But the increase could be blocked by diphenyleneiodonium (DPI), an inhibitor of NADPH oxidase. Meanwhile, cytosolic subunit p47phox moved to membrane and co localizated with gp91phox after irradiation. Moreover, the results also show that gp91phox increased sharply after 12 Gy X ray irradiation. Therefore, NADPH oxidase mediated production of ROS plays an important role in HeLa cell lesion induced by X ray.     

微束技术在放射生物学中的应用

微束装置可以为生命科学研究提供微米定位、剂量特定的电离辐射,在生物体内的电离辐射靶物质及其敏感度、靶物质的损伤及修复机制研究中具有独特的作用。概述了生物微束装置和实验技术的发展及其在低剂量辐射效应、旁观者效应、信号传导研究中的主要应用;介绍了中国科学院近代物理研究所（IMP）重离子微束装置,该装置可以提供能量7~ 80 MeV/u、传能线密度为30~ 3000 keV/μm的重离子微束,实现了活细胞辐照和在线观察、小鼠定位辐照的实验技术;利用IMP微束装置在重离子诱导旁效应实验、小鼠下丘脑重离子辐照效应和DNA损伤快速修复动态等方面取得了一些实验成果。The microbeam facility can provide micrometer scale localized and predefined ionizing radiation in the life science study, and the microbeam techniques play a unique role in determining the target substances of ionizing radiation, as well as in the study of radiation sensitivity, mechanisms of radiation damage response and repair. This paper summarizes the technical developments of biological microbeam facilities and their applications in the studies of low-dose radiation effect, bystander effect and cellular signaling. This paper also introduces the recent developments at the heavy-ion microbeam facility in the Institute of Modern Physics (IMP), which can provide heavy ion microbeam irradiation with energy of 7~80 MeV/u and LET of 30~3000 keV/μm. The facility can perform radiobiological irradiation and online investigation in living cells and mice, including bystander effect study, sleeping system influence after irradiation to mice hypothalamus and the recruitment dynamics of XRCC1 protein.     

Raman spectroscopic study on Hela cells irradiated by X rays of different doses

Raman spectra are used for studying the structure and protein, nucleic acid, lipid, and carbohydrate contents, while cervical cancer cells irradiated by X rays of different doses are cultivated for 24 h. After irradiation by X rays, the following results are obtained. （1） Some 12-Gy groups move to the 1237-cm^-1 band in compared with the control group＇s 1240-cm^-1 band; after irradiation by 6-Gy X ray, the 1662-cm^-1 band of amide I has a blue shift of 10 cm^-1. The above two parts show that because of X ray irradiation, some proteins＇ random coil structures have transformed into β folding. （2） The 759-cm^-1 band disappear in the 6-Gy group; the 570-cm^-1 band of every group has a red shift, but the changes in intensity are different; the 1335-cm^-1 band in every group has a blue shift, and all their intensities increase. These show that although the 570-, 759-, and 1335-cm^-1 bands all belong to the tryptophan residue indole ring vibration, the molecular vibration energy structures which produce scattering lights are different. （3） The 786-cm^-1 band only has a blue shift of 3 cm^-1 in the 6-Gy group, and the non-hydrogen band of the phosphoric acid diester （O-P-O） increases. The frequency deviation of the 1089-cm^-1 band is erratic, and the bent symmetry stretch vibration conformation of phosphoric acid diester key （O=P=O） in the nucleic acid is complex. （4） The 1570-cm^-1 band has a blue shift, and its intensities all decrease, while the C=C conjugated duplet bond oxidizes, and the content of C=C decreases.     

茶多酚对6-OHDA诱导的SH-SY5Y细胞凋亡的保护作用

茶多酚在体内具有广泛的生物活性和药理作用,有助于预防与氧化应激相关的疾病,比如癌症,心血管疾病,神经退行性疾病和衰老. 氧化应激参与了帕金森病（PD）的病理进程. 活性氧在PD的发病机制中发挥了重要的作用,氧自由基直接损伤细胞膜引起脂质过氧化,损伤蛋白质和各种功能酶引起蛋白质沉淀,诱导促凋亡因子的表达,损伤DNA,最终导致了细胞的凋亡. 然而,关于茶多酚对PD的预防和治疗作用目前还不清楚. 本文应用氧化应激诱导的PD病理细胞模型,评价了茶多酚的神经保护作用. 结果表明茶多酚这类植物天然抗氧化剂对氧化应激诱导的细胞凋亡具有明确的抑制作用. 实验中我们选择了6-OHDA诱导的SH-SY5Y细胞作为细胞模型, 运用了MTT、流式细胞术、荧光显微成相, 竞争性ELISA和蛋白质杂交等方法研究了SH-SY5Y细胞的凋亡特性. 结果表明,6-OHDA对SH-SY5Y有时间-浓度依赖性细胞毒性,100 μmol/L 6-OHDA处理24 h,细胞活力减少50 %,同时伴随着活性氧增加（用ＥＳR）,线粒体膜电位降低,细胞内钙离子和一氧化氮增加,nNOS和iNOS表达量上升及蛋白结合的硝基酪氨酸水平升高. 单独茶多酚处理对细胞没有太大的影响,而茶多酚预处理可显著降低6-OHDA所产生的细胞毒性. 溶液实验证明,茶多酚对6-OHDA的自氧化有浓度-时间依赖性抑制作用（用ＥＳＲ）. 本研究表明茶多酚可能是通过活性氧-一氧化氮途径,减少过氧亚硝基的生成来对6-OHDA诱导的细胞凋亡表现保护作用的. 本文的实验结果提示茶多酚在治疗PD等慢性神经退行性疾病上可能是一种有着潜在疗效的药物.     

X射线和过氧化氢引起的Hela细胞染色质损伤的微区拉曼光谱研究

我们成功地用微区拉曼光谱探针技术获得了培养单个活体 Hela 细胞核中染色质的拉曼光谱。从光谱中我们看到正常 Hele 细胞核蛋白的二级结构为 a 螺旋,DNA 为 A 型构象。经10~(-3)moI/L 过氧化氢处理20分钟及8Gy x 射线照射后的 Hela 细胞核蛋白的二级结构出现反平行β折叠,DNA 出现 B 型构象。这种结果与我们的假设是相符合的。     

Fluorescence imaging of reactive oxygen species by confocal laser scanning microscopy for track analysis of synchrotron X‐ray photoelectric nanoradiator dose: X‐ray pump–optical probe

Bursts of emissions of low‐energy electrons, including interatomic Coulomb decay electrons and Auger electrons (0–1000 eV), as well as X‐ray fluorescence produced by irradiation of large‐Z element nanoparticles by either X‐ray photons or high‐energy ion beams, is referred to as the nanoradiator effect. In therapeutic applications, this effect can damage pathological tissues that selectively take up the nanoparticles. Herein, a new nanoradiator dosimetry method is presented that uses probes for reactive oxygen species (ROS) incorporated into three‐dimensional gels, on which macrophages containing iron oxide nanoparticles (IONs) are attached. This method, together with site‐specific irradiation of the intracellular nanoparticles from a microbeam of polychromatic synchrotron X‐rays (5–14 keV), measures the range and distribution of OH radicals produced by X‐ray emission or superoxide anions () produced by low‐energy electrons. The measurements are based on confocal laser scanning of the fluorescence of the hydroxyl radical probe 2‐[6‐(4′‐amino)phenoxy‐3H‐xanthen‐3‐on‐9‐yl] benzoic acid (APF) or the superoxide probe hydroethidine‐dihydroethidium (DHE) that was oxidized by each ROS, enabling tracking of the radiation dose emitted by the nanoradiator. In the range 70 µm below the irradiated cell, radicals derived mostly from either incident X‐ray or X‐ray fluorescence of ION nanoradiators are distributed along the line of depth direction in ROS gel. In contrast, derived from secondary electron or low‐energy electron emission by ION nanoradiators are scattered over the ROS gel. ROS fluorescence due to the ION nanoradiators was observed continuously to a depth of 1.5 mm for both oxidized APF and oxidized DHE with relatively large intensity compared with the fluorescence caused by the ROS produced solely by incident primary X‐rays, which was limited to a depth of 600 µm, suggesting dose enhancement as well as more penetration by nanoradiators. In conclusion, the combined use of a synchrotron X‐ray microbeam‐irradiated three‐dimensional ROS gel and confocal laser scanning fluorescence microscopy provides a simple dosimetry method for track analysis of X‐ray photoelectric nanoradiator radiation, suggesting extensive cellular damage with dose‐enhancement beyond a single cell containing IONs.     

In vivo fate of superparamagnetic iron oxides during sepsis

The enzymatic generation of nitric oxide (NO) in vivo has been reported to be modulated by ions, such as copper and iron. Superparamagnetic iron oxide (SPIO) or ferumoxides is a liver-specific magnetic resonance contrast agent that is taken up by the Kupffer cells, where NO is generated by inducible nitric oxide synthase (iNOS). Thus, it is important to evaluate SPIO in vivo under conditions, such as infectious disease, where significant amounts of NO are generated by iNOS. In this study, we monitored the pharmacokinetics of SPIO in the liver of septic-shock mice and rats. A significant decrease in the ferric iron EPR signal was observed during NO generation in septic-shock mice compared with control mice doped with only SPIO. These results were also confirmed in a model reaction system consisting of SPIO and the NO donor, S-nitroso-N-acetyl DL penicillamine (SNAP). We compared NO generation quantitatively in the liver of the septic-shock rats, either in the presence or absence of SPIO, and found that the presence of SPIO did not affect the NO-generating activity of NOS expressed in the liver. T2-weighted MR images of an agarose gel phantom containing different SPIO to NO donor (SNAP) ratios clearly demonstrated that the contrast enhancement by SPIO decreased with increasing NO at constant SPIO levels. The reduced contrast is most probably due to the reduction of ferric to ferrous irons, resulting in a decrease in paramagnetic relaxation of water protons. These results show that SPIO can be a versatile NO-sensitive indicator, especially employing MRI as a powerful tool to 'visualize' sites of NO generation.     

Ne离子束辐照引起Gd2Ti2O7烧绿石体积肿胀效应研究

在液氮低温下用400 keV的Ne2+离子束对Gd₂Ti₂O₇多晶烧绿石进行了辐照实验研究, 离子束辐照量范围为5×1014—1×1016ions/cm2。利用掠X射线衍射技术对样品辐照层的结构变化进行了分析表征, X射线的掠射角分别为γ=0.25°, 0.5°, 1°和3°。结果表明: 在该实验条件的离子束辐照下, Gd₂Ti₂O₇辐照层会发生明显的体积肿胀效应, 体积肿胀程度随入射离子束辐照量的增大而增大; 在同一辐照量下, 辐照层的体积肿胀程度也随X射线入射角的增大而增大。当辐照量达到1×1016ions/cm2时, 辐照层发生非晶化相变。Polycrystalline pyrochlore Gd₂Ti₂O₇ compounds were irradiated with 400 keV Ne2+ ions at cryogenic temperature (~77 K). The irradiation fluences was ranging from 5×1014 to 1×1016 ions/cm2, corresponding to a peak ballistic damage dose of ~0.16 to 3.3 displacements per atom . Irradiation\|induced structural evolution was examined using grazing incidence X\|ray diffraction (GIXRD) at angles from 0.25° to 3° degrees. It was found that the lattice parameter increases as a function of (1) X\|ray incident angle and (2) ion irradiation fluence, suggesting that the irradiated layer is volumetrically swelled compared with the underlying un\|irradiated substrate. At ion fluence of 1×1016 ions/cm2, the irradiation layer was found to be amorphous.