Compared Analysis of Retinal Protein Expression induced by Neutron Radiation and Microgravity
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摘要: 目的: 本研究采用生物信息学方法分析对比研究中子辐射与微重力环境对鼠视网膜蛋白表达的影响,为理解空间环境对视网膜的损伤机制提供生物学基础,并为空间环境风险评估与防护措施提供参考。
方法:获取中子辐射和微重力作用下老鼠的视网膜蛋白差异表达数据,运用了GO、KEGG富集分析、PPI网络构建及模块分析、Hub蛋白筛选与分析等方法,对比分析中子辐射与微重力对视网膜蛋白差异表达的影响。
结果:GO、KEGG及PPI网络分析结果显示,中子辐射和微重力诱导鼠视网膜蛋白差异表达存在不同。BP、CC、MF最显著富集的功能均不同,中子辐射刺激主要富集在response to xenobiotic stimulus、actin filament和identical protein binding,微重力刺激主要富集在lens development in camera-type eye、mitochondrion和structural constituent of eye lens; KEGG分析结果显示,中子辐射、微重力刺激下Motor proteins通路变化趋势一致,中子辐射刺激还富集在Focal adhesion,Regulation of actin cytoskeleton通路,微重力刺激还富集在Cardiac muscle contraction通路; PPI网络的Hub蛋白(枢纽蛋白)及最显著模块的生物过程不同,中子辐射刺激最显著的生物过程为muscle contraction,微重力刺激最显著的生物过程为camera-type eye development。在中子辐射和微重力刺激下,蛋白PMEL、PTN、TPM1、RAB27A表达变化趋势一致,PDPN出现相反的变化趋势。
结论:视网膜蛋白对中子辐射和微重力刺激的响应存在差异。本研究结果有望初步解释空间辐射或微重力对视网膜损伤的机制,为制定针对性的防护措施提供参考。Abstract: Objective: This study employs bioinformatics methods to analyze and compare the effects of neutron radiation and microgravity environments on retinal protein expression in mice, providing a biological basis for understanding the mechanisms of retinal damage induced by space environments. Furthermore, it offers insights for risk assessment and protective measures related to space environments.
Methods: In this study, we obtained differential expression data of retinal proteins in mice exposed to neutron radiation and microgravity environments. Various bioinformatics methods, including GO and KEGG enrichment analyses, PPI network construction and module analysis, and Hub protein screening and analysis, were employed to compare the effects of neutron radiation and microgravity on retinal protein differential expression.
Results: The results showed that there were differences in the most significantly enriched functions. Neutron radiation inducement primarily enriched in functions such as “response to xenobiotic stimulus”, “actin filament”, and “identical protein binding”. Microgravity inducement enriched in functions such as “lens development in camera-type eye”, “mitochondrion”, and “structural constituent of eye lens”. The KEGG analysis showed that the changes in the “Motor proteins” pathway were consistent under both neutron radiation and microgravity inducement. In addition, neutron radiation inducement also enriched in the “Focal adhesion” and “Regulation of actin cytoskeleton” pathways, while microgravity inducement also enriched in the “Cardiac muscle contraction” pathway. The Hub proteins and biological process (BP) of the most significant modules were different. The most significant BP under neutron radiation inducement was “muscle contraction”, while under microgravity inducement, “camera-type eye development” was the most significant. Under different inducement, the expression trends of proteins PMEL, PTN, TPM1, and RAB27A were consistent. However, PDPN showed an opposite change.
Conclusion: The study results suggest that retinal proteins respond differently to neutron radiation and microgravity stimuli. These findings have the potential to elucidate the mechanisms of retinal damage caused by space radiation or microgravity and provide a reference for developing targeted protective measures.-
Key words:
- neutron radiation /
- microgravity /
- retina /
- differentially expressed protein
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