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急性放射性暴露后延迟效应的潜在起始事件:WTLI 后小鼠肺中的急性蛋白质组变化。

Acute Proteomic Changes in the Lung After WTLI in a Mouse Model: Identification of Potential Initiating Events for Delayed Effects of Acute Radiation Exposure.

机构信息

University of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, MD.

University of Maryland, School of Medicine, Department of Radiation Oncology, Baltimore, MD.

出版信息

Health Phys. 2019 Apr;116(4):503-515. doi: 10.1097/HP.0000000000000956.

Abstract

Radiation-induced lung injury is a delayed effect of acute radiation exposure resulting in pulmonary pneumonitis and fibrosis. Molecular mechanisms that lead to radiation-induced lung injury remain incompletely understood. Using a murine model of whole-thorax lung irradiation, C57BL/6J mice were irradiated at 8, 10, 12, and 14 Gy and assayed at day 1, 3, and 6 postexposure and compared to nonirradiated (sham) controls. Tryptic digests of lung tissues were analyzed by liquid chromatography-tandem mass spectrometry on a Waters nanoLC instrument coupled to a Thermo Scientific Q Exactive hybrid quadrupole-orbitrap mass spectrometer. Pathway and gene ontology analysis were performed with Qiagen Ingenuity, Panther GO, and DAVID databases. A number of trends were identified in the proteomic data, including protein changes greater than 10 fold, protein changes that were consistently up regulated or down regulated at all time points and dose levels interrogated, time and dose dependency of protein changes, canonical pathways affected by irradiation, changes in proteins that serve as upstream regulators, and proteins involved in key processes including inflammation, radiation, and retinoic acid signaling. The proteomic profiling conducted here represents an untargeted systems biology approach to identify acute molecular events that could potentially be initiating events for radiation-induced lung injury.

摘要

放射性肺损伤是急性放射性暴露导致的肺肺炎和纤维化的延迟效应。导致放射性肺损伤的分子机制仍不完全清楚。使用全胸肺照射的小鼠模型,将 C57BL/6J 小鼠在 8、10、12 和 14 Gy 下照射,并在暴露后第 1、3 和 6 天进行检测,并与未经照射(假)对照进行比较。用 Waters nanoLC 仪器与 Thermo Scientific Q Exactive 杂交四极杆轨道阱质谱仪联用,对肺组织的胰蛋白酶消化物进行液相色谱-串联质谱分析。采用 Qiagen Ingenuity、Panther GO 和 DAVID 数据库进行途径和基因本体分析。蛋白质组学数据中确定了一些趋势,包括蛋白变化大于 10 倍,蛋白变化在所有时间点和剂量水平上一致上调或下调,蛋白变化的时间和剂量依赖性,受照射影响的经典途径,作为上游调节剂的蛋白变化,以及涉及炎症、辐射和维甲酸信号转导等关键过程的蛋白。这里进行的蛋白质组学分析代表了一种非靶向系统生物学方法,可用于识别可能引发放射性肺损伤的急性分子事件。

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