Kurarinone regulates Th17/Treg balance and ameliorates autoimmune uveitis via Rac1 inhibition

被引:2
|
作者
Gu, Chenyang [1 ]
Liu, Yidan [1 ]
Lv, Jianjie [1 ]
Zhang, Chun [2 ]
Huang, Zhaohao [1 ]
Jiang, Qi [1 ]
Gao, Yuehan [1 ]
Tao, Tianyu [1 ]
Su, Yuhan [1 ,3 ]
Chen, Binyao [1 ]
Jia, Renbing [4 ]
Liu, Xiuxing [1 ]
Su, Wenru [1 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Ophthalmol, Guangdong Prov Key Lab Ophthalmol & Visual Sci, Guangzhou 510060, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Ophthalmol, Chengdu 610041, Sichuan, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Clin Med, Guangzhou 510060, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Ophthalmol, Shanghai Key Lab Orbital Dis & Ocular Oncol,Sch Me, Shanghai 200011, Peoples R China
关键词
Autoimmune uveitis; Kurarinone; Th17; Rac1; Treg; Single-cell RNA sequencing; T-CELLS; T(H)17 CELLS; TREG CELLS; TH17; FLAVONOIDS; JAK/STAT; GTPASES;
D O I
10.1016/j.jare.2024.03.013
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Autoimmune uveitis (AU) is a severe intraocular autoimmune disorder with a chronic disease course and a high rate of blindness. Kurarinone (KU), a major component of the traditional Chinese medicine Sophorae Flavescentis Radix, possesses a wide spectrum of activities and has been used to treat several inflammation-related diseases. Objective: We aimed to investigate the effects of KU on AU and its modulatory mechanisms. Methods: We used an experimental autoimmune uveitis (EAU) animal model and characterized the com- prehensive immune landscape of KU-treated EAU mice using single-cell RNA sequencing (scRNA-seq). The retina and lymph nodes were analyzed. The siRNAs and selective inhibitors were used to study the signaling pathway. The effect of KU on peripheral blood mononuclear cells (PBMCs) from uveitis patients was also examined. Results: We found that KU relieved chorioretinal lesions and immune cell infiltration in EAU model mice. Subsequent single-cell analysis revealed that KU downregulated the EAU-upregulated expression of inflammatory and autoimmune-related genes and suppressed pathways associated with immune cell dif- ferentiation, activation, and migration in a cell-specific manner. KU was implicated in restoring T helper 17 (Th17)/regulatory T (Treg) cell balance by alleviating inflammatory injury and elevating the expres- sion of modulatory mediators in Tregs, while simultaneously ameliorating excessive inflammation by Th17 cells. Furthermore, Rac1 and the Id2/Pim1 axis potentiated the pathogenicity of Th17 cells during EAU, which was inhibited by KU treatment, contributing to the amelioration of EAU-induced inflamma- tion and treatment of AU. In addition, KU suppressed inflammatory cytokine production in activated human PBMCs by inhibiting Rac1. Integration of the glucocorticoid-treated transcriptome suggests that KU has immunomodulatory effects on lymphocytes. Conclusion: Our study constructed a high-resolution atlas of the immunoregulatory effects of KU treat- ment on EAU and identified its potential therapeutic mechanisms, which hold great promise in treating autoimmune disorders. (c) 2024 Production and hosting by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:381 / 398
页数:18
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