{"title":"通过增强EsGSK3β活性抑制Wnt信号通路,促进螺旋体感染,导致甲壳类动物的神经性疾病。","authors":"Libo Hou, Yu Yao, Yubo Ma, Wei Gu, Wen Wang, Wei Sun, Qingguo Meng","doi":"10.1016/j.mcpro.2025.101059","DOIUrl":null,"url":null,"abstract":"<p><p>Spiroplasma eriocheiris has been identified as a lethal pathogen of Eriocheir sinensis tremor disease (TD), one neurological disease with typically paroxysmal tremors of the pereiopod. But, the pathogenic mechanism of TD was still unknown. First, in the current study, the phosphoproteomic changes of E. sinensis thoracic ganglion after S. eriocheiris infection were obtained using TMT labeling and affinity enrichment followed by high-resolution LC-MS/MS analysis. A total of 349 phosphorylation proteins are upregulated, and 331 phosphorylation proteins are downregulated when compared to the control sample with quantitative ratios above 1.5 or below 1/1.5 that are deemed significant. Bioinformatics analysis (Gene ontology, Kyoto Encyclopedia of Genes and Genomes pathway, and domain analysis, etc.) showed that Wnt signaling pathways were restrained, corresponding to many nervous system developments, and signal transmission pathway was also disrupted. Neurotransmitter metabolite analysis showed metabolic dysregulation of four key neurotransmitters (5-Hydroxy-L-tryptophan, serotonin, acetylcholine, and γ-amino-butyric acid) in thoracic ganglion of E. sinensis following S. eriocheiris infection. Second, similar to its effects on the thoracic ganglion cells, S. eriocheiris infection of hemocytes (the primary target cells and most crucial immune cells in crabs) also suppressed the host Wnt pathway through enhanced EsGSK3β activity, both in vivo and in vitro. Co-immunoprecipitation analysis showed that EsGSK3β could directly interact with Esβ-catenin. Inhibited or enhanced EsGSK3β activity of hemocytes could reduce or facilitate S. eriocheiris infection by regulating the stability and nuclear translocation of Esβ-catenin. Finally, further analysis showed that Wnt-β-catenin pathway could functionally crosstalk with Toll pathway to positively regulate hemocytes antibacterial peptides transcription. Altogether, our results suggest that S. eriocheiris could restrain the crab Wnt pathway, reduce antibacterial peptides transcription to help its infection and disorder neurotransmitters to cause neuropathic TD at last.</p>","PeriodicalId":18712,"journal":{"name":"Molecular & Cellular Proteomics","volume":" ","pages":"101059"},"PeriodicalIF":5.5000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482308/pdf/","citationCount":"0","resultStr":"{\"title\":\"Restrained Wnt Signaling Pathway by Enhanced EsGSK3β Activity Facilitates the Infection of Spiroplasma and Leads to Neuropathic Diseases in Crustaceans.\",\"authors\":\"Libo Hou, Yu Yao, Yubo Ma, Wei Gu, Wen Wang, Wei Sun, Qingguo Meng\",\"doi\":\"10.1016/j.mcpro.2025.101059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Spiroplasma eriocheiris has been identified as a lethal pathogen of Eriocheir sinensis tremor disease (TD), one neurological disease with typically paroxysmal tremors of the pereiopod. But, the pathogenic mechanism of TD was still unknown. First, in the current study, the phosphoproteomic changes of E. sinensis thoracic ganglion after S. eriocheiris infection were obtained using TMT labeling and affinity enrichment followed by high-resolution LC-MS/MS analysis. A total of 349 phosphorylation proteins are upregulated, and 331 phosphorylation proteins are downregulated when compared to the control sample with quantitative ratios above 1.5 or below 1/1.5 that are deemed significant. Bioinformatics analysis (Gene ontology, Kyoto Encyclopedia of Genes and Genomes pathway, and domain analysis, etc.) showed that Wnt signaling pathways were restrained, corresponding to many nervous system developments, and signal transmission pathway was also disrupted. Neurotransmitter metabolite analysis showed metabolic dysregulation of four key neurotransmitters (5-Hydroxy-L-tryptophan, serotonin, acetylcholine, and γ-amino-butyric acid) in thoracic ganglion of E. sinensis following S. eriocheiris infection. Second, similar to its effects on the thoracic ganglion cells, S. eriocheiris infection of hemocytes (the primary target cells and most crucial immune cells in crabs) also suppressed the host Wnt pathway through enhanced EsGSK3β activity, both in vivo and in vitro. Co-immunoprecipitation analysis showed that EsGSK3β could directly interact with Esβ-catenin. Inhibited or enhanced EsGSK3β activity of hemocytes could reduce or facilitate S. eriocheiris infection by regulating the stability and nuclear translocation of Esβ-catenin. Finally, further analysis showed that Wnt-β-catenin pathway could functionally crosstalk with Toll pathway to positively regulate hemocytes antibacterial peptides transcription. Altogether, our results suggest that S. eriocheiris could restrain the crab Wnt pathway, reduce antibacterial peptides transcription to help its infection and disorder neurotransmitters to cause neuropathic TD at last.</p>\",\"PeriodicalId\":18712,\"journal\":{\"name\":\"Molecular & Cellular Proteomics\",\"volume\":\" \",\"pages\":\"101059\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482308/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular & Cellular Proteomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.mcpro.2025.101059\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular & Cellular Proteomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mcpro.2025.101059","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
摘要
中华绒螯螯螺原体是中国绒螯螯震颤病的致死性病原体。绒螯螯震颤病是一种典型的四肢类动物阵发性震颤的神经系统疾病。但TD的发病机制尚不清楚。首先,本研究采用TMT标记和亲和富集的方法,结合高分辨率LC-MS/MS分析,获得了中华赤芍胸椎神经节感染棘球蚴后的磷酸化蛋白质组学变化。与对照样品相比,共有349个磷酸化蛋白上调,331个磷酸化蛋白下调,定量比高于1.5或低于1/1.5被认为显著。生物信息学分析(GO、KEGG通路、Domain分析等)显示Wnt信号通路受到抑制,相应的许多神经系统发育和信号传递通路也被破坏。神经递质代谢物分析显示,中华中华弓形虫感染后胸神经节中4种关键神经递质(5-羟基- l -色氨酸、5-羟色胺、乙酰胆碱和γ-氨基丁酸)代谢失调。其次,与其对胸神经节细胞的作用类似,在体内和体外实验中,S. eriocheiris感染血细胞(蟹的主要靶细胞和最关键的免疫细胞)也通过增强EsGSK3β活性抑制宿主Wnt通路。共免疫沉淀(Co-IP)分析表明,EsGSK3β可直接与Esβ-catenin相互作用。抑制或增强血细胞EsGSK3β活性可通过调节esβ -连环蛋白的稳定性和核易位来减少或促进衣毛弧菌感染。最后,进一步分析发现Wnt-β-catenin通路可与Toll通路功能性串扰,正向调节血细胞抗菌肽(antimicrobial peptides, AMP)转录。综上所述,我们的研究结果表明,毛毛棘球菌可以抑制螃蟹Wnt通路,降低AMP转录,最终帮助其感染和紊乱神经递质,导致神经性TD。
Restrained Wnt Signaling Pathway by Enhanced EsGSK3β Activity Facilitates the Infection of Spiroplasma and Leads to Neuropathic Diseases in Crustaceans.
Spiroplasma eriocheiris has been identified as a lethal pathogen of Eriocheir sinensis tremor disease (TD), one neurological disease with typically paroxysmal tremors of the pereiopod. But, the pathogenic mechanism of TD was still unknown. First, in the current study, the phosphoproteomic changes of E. sinensis thoracic ganglion after S. eriocheiris infection were obtained using TMT labeling and affinity enrichment followed by high-resolution LC-MS/MS analysis. A total of 349 phosphorylation proteins are upregulated, and 331 phosphorylation proteins are downregulated when compared to the control sample with quantitative ratios above 1.5 or below 1/1.5 that are deemed significant. Bioinformatics analysis (Gene ontology, Kyoto Encyclopedia of Genes and Genomes pathway, and domain analysis, etc.) showed that Wnt signaling pathways were restrained, corresponding to many nervous system developments, and signal transmission pathway was also disrupted. Neurotransmitter metabolite analysis showed metabolic dysregulation of four key neurotransmitters (5-Hydroxy-L-tryptophan, serotonin, acetylcholine, and γ-amino-butyric acid) in thoracic ganglion of E. sinensis following S. eriocheiris infection. Second, similar to its effects on the thoracic ganglion cells, S. eriocheiris infection of hemocytes (the primary target cells and most crucial immune cells in crabs) also suppressed the host Wnt pathway through enhanced EsGSK3β activity, both in vivo and in vitro. Co-immunoprecipitation analysis showed that EsGSK3β could directly interact with Esβ-catenin. Inhibited or enhanced EsGSK3β activity of hemocytes could reduce or facilitate S. eriocheiris infection by regulating the stability and nuclear translocation of Esβ-catenin. Finally, further analysis showed that Wnt-β-catenin pathway could functionally crosstalk with Toll pathway to positively regulate hemocytes antibacterial peptides transcription. Altogether, our results suggest that S. eriocheiris could restrain the crab Wnt pathway, reduce antibacterial peptides transcription to help its infection and disorder neurotransmitters to cause neuropathic TD at last.
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