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Live-cell imaging to detect phosphatidylserine externalization in brain endothelial cells exposed to ionizing radiation : implications for the treatment of brain arteriovenous malformations

机译:活细胞成像检测暴露于电离辐射的脑内皮细胞中的磷脂酰丝氨酸外在化:对治疗脑动静脉畸形的意义

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摘要

Objective: Stereotactic radiosurgery (SRS) is an established intervention for brain arteriovenous malformations (AVMs). The processes of AVM vessel occlusion after SRS are poorly understood. To improve SRS efficacy, it is important to understand the cellular response of blood vessels to radiation. The molecular changes on the surface of AVM endothelial cells after irradiation may also be used for vascular targeting. This study investigates radiation-induced externalization of phosphatidylserine (PS) on endothelial cells using live-cell imaging. Methods: An immortalized cell line generated from mouse brain endothelium, bEnd.3 cells, was cultured and irradiated at different radiation doses using a linear accelerator. PS externalization in the cells was subsequently visualized using polarity-sensitive indicator of viability and apoptosis (pSIVA)-IANBD, a polarity-sensitive probe. Live-cell imaging was used to monitor PS externalization in real time. The effects of radiation on the cell cycle of bEnd.3 cells were also examined by flow cytometry. Results: Ionizing radiation effects are dose dependent. Reduction in the cell proliferation rate was observed after exposure to 5 Gy radiation, whereas higher radiation doses (15 Gy and 25 Gy) totally inhibited proliferation. In comparison with cells treated with sham radiation, the irradiated cells showed distinct pseudopodial elongation with little or no spreading of the cell body. The percentages of pSIVA-positive cells were significantly higher (p = 0.04) 24 hours after treatment in the cultures that received 25- and 15-Gy doses of radiation. This effect was sustained until the end of the experiment (3 days). Radiation at 5 Gy did not induce significant PS externalization compared with the sham-radiation controls at any time points (p > 0.15). Flow cytometric analysis data indicate that irradiation induced growth arrest of bEnd.3 cells, with cells accumulating in the G2 phase of the cell cycle. Conclusions: Ionizing radiation causes remarkable cellular changes in endothelial cells. Significant PS externalization is induced by radiation at doses of 15 Gy or higher, concomitant with a block in the cell cycle. Radiation-induced markers/targets may have high discriminating power to be harnessed in vascular targeting for AVM treatment.
机译:目的:立体定向放射外科(SRS)是针对脑动静脉畸形(AVM)的既定干预措施。对SRS后AVM血管闭塞的过程了解甚少。为了提高SRS功效,重要的是了解血管对辐射的细胞反应。辐照后AVM内皮细胞表面的分子变化也可用于血管靶向。这项研究调查了使用活细胞成像辐射诱导内皮细胞磷脂酰丝氨酸(PS)的外在化。方法:培养小鼠脑内皮细胞永生化的bEnd.3细胞系,并使用线性加速器以不同的辐射剂量进行辐照。随后使用极性敏感的生存力和细胞凋亡指示剂(pSIVA)-IANBD(极性敏感的探针)观察细胞中的PS外部化。活细胞成像用于实时监测PS外部化。还通过流式细胞术检查了辐射对bEnd.3细胞的细胞周期的影响。结果:电离辐射效应是剂量依赖性的。暴露于5 Gy辐射后观察到细胞增殖速率降低,而较高的辐射剂量(15 Gy和25 Gy)则完全抑制了增殖。与用假放射线处理的细胞相比,被照射的细胞显示出明显的假足伸长,几乎没有或没有细胞体扩散。在接受25和15 Gy辐射剂量的培养物中,处理后24小时pSIVA阳性细胞的百分比明显更高(p = 0.04)。这种作用一直持续到实验结束(3天)。在任何时间点,与假辐射对照组相比,在5 Gy的辐射下均不会引起明显的PS外在化(p> 0.15)。流式细胞仪分析数据表明,辐射诱导了bEnd.3细胞的生长停滞,其中细胞在细胞周期的G2期积累。结论:电离辐射引起内皮细胞的显着细胞变化。 15 Gy或更高剂量的辐射伴随细胞周期受阻而引起大量PS外部化。辐射诱导的标记物/靶标可能具有高识别力,可用于血管靶向治疗AVM。

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