Suppr超能文献

蛋白质组学分析与临床见解:基质金属蛋白酶9在寻常型银屑病与泛发性脓疱型银屑病鉴别诊断中的作用

Proteomic Profiling and Clinical Insights: The Role of MMP9 in Differentiating Psoriasis Vulgaris from Generalized Pustular Psoriasis.

作者信息

Gong Ting, Chen Jiawen, Xiao Zhixun, Luo Renwei, Tong Zequn, Ke Hui, Liu Zhao, Xiao Cuirong, Xiang Niu, Ji Chao

机构信息

Central Laboratory, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, 350000, People's Republic of China.

Department of Dermatology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, 350000, People's Republic of China.

出版信息

J Inflamm Res. 2025 Mar 14;18:3795-3805. doi: 10.2147/JIR.S495044. eCollection 2025.

Abstract

BACKGROUND

Generalized pustular psoriasis (GPP) constitutes a rare, severe inflammatory disorder that differs from psoriasis vulgaris (PV). The IL-36 pathway has been identified as a key element in GPP pathogenesis.

OBJECTIVE

To explore protein expression between PV and GPP, providing insights into potential mechanisms.

METHODS

We performed proteomic analysis of tissue specimens from patients with PV and GPP to identify differentially expressed proteins. Comparative analysis of the proteomic data was performed and proteins with significant differences were further identified using immunofluorescence and Western blot techniques. Differential proteins were also explored by evaluating the efficacy of IL-36R inhibitors before and after GPP treatment, providing potential avenues for targeted therapeutic strategies.

RESULTS

Tissue proteomic profiling showed that matrix metallopeptidase 9 (MMP9) increased significantly in the GPP as compared to PV. Immunofluorescence and Western blot analysis confirmed that MMP9 is higher expressed in GPP. And after therapy with IL-36 inhibitors showed that the level of MMP9 expression was markedly reduced.

CONCLUSION

MMP9 may be involved with the pathogenesis of GPP.

摘要

背景

泛发性脓疱型银屑病(GPP)是一种罕见的严重炎症性疾病,与寻常型银屑病(PV)不同。白细胞介素-36(IL-36)通路已被确定为GPP发病机制中的关键因素。

目的

探讨PV和GPP之间的蛋白质表达情况,为潜在机制提供见解。

方法

我们对PV和GPP患者的组织标本进行蛋白质组学分析,以鉴定差异表达的蛋白质。对蛋白质组学数据进行比较分析,并使用免疫荧光和Western印迹技术进一步鉴定有显著差异的蛋白质。还通过评估GPP治疗前后IL-36R抑制剂的疗效来探索差异蛋白,为靶向治疗策略提供潜在途径。

结果

组织蛋白质组学分析表明,与PV相比,GPP中基质金属蛋白酶9(MMP9)显著增加。免疫荧光和Western印迹分析证实,MMP9在GPP中表达更高。并且在用IL-36抑制剂治疗后,MMP9的表达水平明显降低。

结论

MMP9可能参与GPP的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/683e/11920628/8f6a197a86eb/JIR-18-3795-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验