Construction of janus mesenchymal stem cell-hitchhiked melanin nanoparticles to modulate the Th17/Treg balance for rheumatoid arthritis therapy

被引:2
作者
Han, Xiaoqing [1 ,2 ]
Song, Panpan [3 ,4 ]
Cai, Rui [5 ]
Zhu, Heng [6 ,7 ]
Yan, Jiao [3 ,4 ]
Wang, Xingbo [2 ]
Wang, Yanjing [3 ,4 ]
Kang, Yaqing [2 ]
Ma, Yuting [6 ,7 ]
Wang, Liming [3 ,4 ,5 ]
Zhang, Haiyuan [3 ,4 ]
机构
[1] Northeast Normal Univ, Key Lab Mol Epigenet, Minist Educ MOE, Changchun, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Lab Chem Biol, Changchun, Peoples R China
[3] Guangzhou Med Univ, Sch Biomed Engn, Guangzhou, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou, Peoples R China
[5] Chinese Acad Sci, Inst High Energy Phys, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing, Peoples R China
[6] Univ Sci & Technol China, Sch Biomed Engn Suzhou, Div Life Sci & Med, Hefei, Peoples R China
[7] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, CAS Key Lab Biomed Diag, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Rheumatoid Arthritis; Janus Mesenchymal Stem Cells; Hitchhiking; Long-acting Th17/Treg Balance; Immunoregulation; Melanin Nanoparticles; T-CELL; DELIVERY; BLOOD; TREG;
D O I
10.1016/j.nantod.2024.102322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rheumatoid arthritis (RA) is a common chronic inflammatory disease capable of causing the disability. Although various antioxidant strategies have been attempted for prevention and treatment of RA through scavenging the free radicals, the therapeutic effect is limited. Recently, it is reported that the unremitting course of RA intensely correlates with the persistence of immunologic memory, in which the imbalance of T helper 17 (Th17) cells/ regulatory T (Treg) cells plays an important role. Herein, we constructed Janus mesenchymal stem cell (MSC)hitchhiked melanin nanoparticles (MSC FM ) for RA therapy, where one half of MSC kept intact for chemotactically migrating towards the RA inflammatory sites and efficiently restoring the Th17/Treg balance based on the property of MSCs, while the other half hitchhiked the iron -doped melanin (FM) nanoparticles (NPs) and release them to scavenge free radicals for maintaining the durability of Th17/Treg balance. In vitro studies indicated MSC FM could migrate towards CXCL12 inflammatory cytokine, scavenge reactive oxygen and nitrogen species, inhibit Th17 cell proliferation and induce Treg cell production. Further in vivo studies corroborated that intravenously injected MSC FM could target the RA site of collagen -induced arthritis mouse model and alleviate the pathological progression of RA. MSC FM holds great potential as an anti-inflammatory agent for RA management.
引用
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页数:13
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