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利用细胞荧光离子径迹混合探测器进行粒子辐照物理能量沉积与细胞反应空间相关性的登记程序。

Registration procedure for spatial correlation of physical energy deposition of particle irradiation and cellular response utilizing cell-fluorescent ion track hybrid detectors.

作者信息

Niklas M, Zimmermann F, Schlegel J, Schwager C, Debus J, Jäkel O, Abdollahi A, Greilich S

机构信息

Molecular & Translational Radiation Oncology, National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany. German Cancer Consortium (DKTK), D-69120 Heidelberg, Germany. Heidelberg Institute of Radiation Oncology (HIRO), National Center for Radiation Research in Oncology (NCRO), D-69120 Heidelberg, Germany.

出版信息

Phys Med Biol. 2016 Sep 7;61(17):N441-60. doi: 10.1088/0031-9155/61/17/N441. Epub 2016 Aug 8.

DOI:10.1088/0031-9155/61/17/N441
PMID:27499388
Abstract

The hybrid technology cell-fluorescent ion track hybrid detector (Cell-Fit-HD) enables the investigation of radiation-related cellular events along single ion tracks on the subcellular scale in clinical ion beams. The Cell-Fit-HD comprises a fluorescent nuclear track detector (FNTD, the physical compartment), a device for individual particle detection and a substrate for viable cell-coating, i.e. the biological compartment. To date both compartments have been imaged sequentially in situ by confocal laser scanning microscopy (CLSM). This is yet in conflict with a functional read-out of the Cell-Fit-HD utilizing a fast live-cell imaging of the biological compartment with low phototoxicity on greater time scales. The read-out of the biological from the physical compartment was uncoupled. A read-out procedure was developed to image the cell layer by conventional widefield microscopy whereas the FNTD was imaged by CLSM. Point mapping registration of the confocal and widefield imaging data was performed. Non-fluorescent crystal defects (spinels) visible in both read-outs were used as control point pairs. The accuracy achieved was on the sub-µm scale. The read-out procedure by widefield microscopy does not impair the unique ability of spatial correlation by the Cell-Fit-HD. The uncoupling will enlarge the application potential of the hybrid technology significantly. The registration allows for an ultimate correlation of microscopic physical beam parameters and cell kinetics on greater time scales. The method reported herein will be instrumental for the introduction of a novel generation of compact detectors facilitating biodosimetric research towards high-throughput analysis.

摘要

混合技术细胞荧光离子径迹混合探测器(Cell-Fit-HD)能够在临床离子束的亚细胞尺度上沿着单离子径迹研究与辐射相关的细胞事件。Cell-Fit-HD包括一个荧光核径迹探测器(FNTD,物理部分)、一个用于单个粒子检测的装置和一个用于活细胞包被的基质,即生物部分。迄今为止,这两个部分已通过共聚焦激光扫描显微镜(CLSM)原位顺序成像。然而,这与在更长时间尺度上对生物部分进行具有低光毒性的快速活细胞成像来实现Cell-Fit-HD的功能读出相冲突。将生物部分从物理部分的读出解耦。开发了一种读出程序,通过传统宽场显微镜对细胞层成像,而通过CLSM对FNTD成像。对共聚焦和宽场成像数据进行点映射配准。在两个读出中可见的非荧光晶体缺陷(尖晶石)用作控制点对。实现的精度在亚微米尺度。宽场显微镜的读出程序不会损害Cell-Fit-HD独特的空间关联能力。这种解耦将显著扩大混合技术的应用潜力。配准允许在更长时间尺度上对微观物理束参数和细胞动力学进行最终关联。本文报道的方法将有助于引入新一代紧凑型探测器,促进生物剂量学研究向高通量分析发展。

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