Acute Proteomic Changes in Lung after Radiation: Toward Identifying Initiating Events of Delayed Effects of Acute Radiation Exposure in Non-human Primate after Partial Body Irradiation with Minimal Bone Marrow Sparing

被引:10
|
作者
Huang, Weiliang [1 ]
Yu, Jianshi [1 ]
Liu, Tian [1 ]
Defnet, Amy E. [1 ]
Zalesak-Kravec, Stephanie [1 ]
Farese, Ann M. [2 ]
MacVittie, Thomas J. [2 ]
Kane, Maureen A. [1 ]
机构
[1] Univ Maryland, Dept Pharmaceut Sci, Sch Pharm, 20 N Pine St,Room N731, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Radiat Oncol, Baltimore, MD 21201 USA
来源
HEALTH PHYSICS | 2021年 / 121卷 / 04期
基金
美国国家卫生研究院;
关键词
biological indicators; lungs; human; radiation damage; radiation; ionizing; ENDOGENOUS RETINOIC ACID; UNION-OF-PHARMACOLOGY; REGULATORY T-CELLS; GENE-EXPRESSION; BIOMARKER PANEL; IN-VITRO; INJURY; QUANTIFICATION; IDENTIFICATION; PLASMA;
D O I
10.1097/HP.0000000000001476
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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 non-human primate model of partial body irradiation with minimal bone marrow sparing, lung was analyzed from animals irradiated with 12 Gy at timepoints every 4 d up to 21 d after irradiation and compared to non-irradiated (sham) controls. Tryptic digests of lung tissues were analyzed by liquid chromatography-tandem mass spectrometry followed by pathway analysis. Out of the 3,101 unique proteins that were identified, we found that 252 proteins showed significant and consistent responses across at least three time points post-irradiation, of which 215 proteins showed strong up-regulation while 37 proteins showed down-regulation. Canonical pathways affected by irradiation, changes in proteins that serve as upstream regulators, and proteins involved in key processes including inflammation, fibrosis, and retinoic acid signaling were identified. The proteomic profiling of lung conducted here represents an untargeted systems biology approach to identify acute molecular events in the non-human primate lung that could potentially be initiating events for radiation-induced lung injury.
引用
收藏
页码:384 / 394
页数:11
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