Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang
{"title":"系统性红斑狼疮不同疾病阶段核蛋白改变的分子特征。","authors":"Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang","doi":"10.1021/acs.jproteome.5c00645","DOIUrl":null,"url":null,"abstract":"<p><p>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.</p>","PeriodicalId":48,"journal":{"name":"Journal of Proteome Research","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular Signatures of Nuclear Protein Alterations in Systemic Lupus Erythematosus across Disease Stages.\",\"authors\":\"Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang\",\"doi\":\"10.1021/acs.jproteome.5c00645\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.</p>\",\"PeriodicalId\":48,\"journal\":{\"name\":\"Journal of Proteome Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Proteome Research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jproteome.5c00645\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Proteome Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.5c00645","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Molecular Signatures of Nuclear Protein Alterations in Systemic Lupus Erythematosus across Disease Stages.
Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.
期刊介绍:
Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".