Autoantibody Reactome Profiling Reveals Distinct Humoral Immune Signatures Induced by Simulated Microgravity, Radiation, and Combined Exposure in Mice.

IF 6.3 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Lining Wu, Kaipeng Zheng, Bomiao Yu, Bingxin Gao, Pancheng Xiao, Saiya Wang, Yanjun Li, Ruimin Liu, Xiaomei Zhang, Mansheng Li, Chun-Ping Cui, Weiming Tian, Xiaobo Yu
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Abstract

Microgravity (μG) and space radiation are major environmental stressors leading to immune dysfunction in astronauts, but the mechanisms governing humoral immunity and effective interventions remain unclear. In this study, we used a high-throughput autoantigen microarray derived from the AAgAtlas 1.0 database to profile humoral immune responses in mice exposed to μG and proton irradiation. We generated 70,490 autoantibody reactivity measurements and observed combined effects of radiation and μG on humoral immunity. Specifically, 38 IgM and 57 IgG autoantibody candidates showed dose-associated changes across 0, 1 and 5 Gy proton irradiation. We further established a global autoantibody landscape for mice under μG, 1 Gy, 5 Gy and μG & 1 Gy. Autoantibody targets altered under μG were enriched for cardiovascular-associated proteins, whereas proton irradiation-associated targets were enriched for DNA repair-related proteins and co-exposure-associated targets were enriched for inflammation-related proteins, revealing distinct humoral immune recognition signatures across exposure conditions. Additionally, a glutamine-free diet (GFD) was associated with changes in autoantibody profiles and shifts in selected bone and hematological parameters toward control levels under μG and μG & 1 Gy conditions. This work provides a resource for investigating humoral immunity under space-related stress and identifies candidate autoantibody signatures and a potential role of dietary modulation that warrant further validation.

自身抗体反应组分析揭示了模拟微重力、辐射和联合暴露在小鼠体内诱导的独特体液免疫特征。
微重力和空间辐射是导致宇航员免疫功能障碍的主要环境应激源,但体液免疫的调控机制和有效干预措施尚不清楚。在这项研究中,我们使用来自AAgAtlas 1.0数据库的高通量自身抗原微阵列来分析暴露于μG和质子照射的小鼠的体液免疫反应。我们进行了70,490次自身抗体反应性测量,观察了辐射和μG对体液免疫的联合影响。具体来说,38个IgM和57个IgG自身抗体候选物在0、1和5 Gy质子辐照中显示出剂量相关的变化。我们进一步建立了小鼠在μG、1 Gy、5 Gy和μG & 1 Gy作用下的全局自身抗体图谱。在μG下改变的自身抗体靶标富集了心血管相关蛋白,而质子照射相关靶标富集了DNA修复相关蛋白,共暴露相关靶标富集了炎症相关蛋白,揭示了不同暴露条件下不同的体液免疫识别特征。此外,在μG和μG & 1gy条件下,无谷氨酰胺饮食(GFD)与自身抗体谱的变化以及选定的骨骼和血液学参数向控制水平的变化有关。这项工作为研究空间相关应激下的体液免疫提供了资源,并确定了候选自身抗体特征和饮食调节的潜在作用,这些需要进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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