Celastrol-loaded bovine serum albumin nanoparticles target inflamed neutrophils for improved rheumatoid arthritis therapy

被引:15
作者
Liu, Siyi [1 ]
Liu, Min [1 ]
Xiu, Jingya [1 ]
Zhang, Tian [1 ]
Zhang, Bowen [1 ]
Cun, Dongyun [2 ]
Yang, Chunrong [3 ]
Li, Kexin [1 ]
Zhang, Jiulong [1 ]
Zhao, Xiuli [1 ]
机构
[1] Shenyang Pharmaceut Univ, Coll Pharm, Shenyang 110000, Peoples R China
[2] Kunming Med Univ, Affiliated Hosp 2, Dept Hepatopancreatobiliary Surg, Kunming 650101, Peoples R China
[3] Shantou Univ, Dept Pharm, Med Coll, Shantou 515000, Peoples R China
关键词
Rheumatoid arthritis; Celastrol; Inflammatory neutrophils; Apoptosis; Neutrophil extracellular traps; EXTRACELLULAR TRAPS;
D O I
10.1016/j.actbio.2023.11.028
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Inflammatory neutrophils (INEs), motivated by cytokines, continue to migrate into the inflamed joints, driving the development of RA. Hence, inducing apoptosis of INEs to reduce recruitment at inflamed joints is an effective strategy for the treatment of RA. However, simply apoptotic INEs may trigger the release of neutrophil extracellular traps (NETs) and accelerate the inflammatory process. To overcome these drawbacks, an RGD-modified bovine serum albumin (BSA) nanoparticles (CBR NPs) was fabricated to selectively target INEs in situ for intracellular delivery of CLT. Studies have demonstrated that CBR NPs can selectively target circulating INEs and induce INEs apoptosis. Meanwhile, CBR NPs inhibited the activation of NETs via NF-kappa B pathway and the release of Cit-H3 thereby blocking the release process of NETs. In collagen-induced arthritis (CIA) mouse model, CBR NPs suppressed the inflammatory response, and reduced the toxic effects of CLT. In summary, this study shed light on an innovative approach to treat RA by inducing apoptosis of circulating INEs and inhibiting NETs. Statement of Significance RGD-modified bovine serum albumin (BSA) nanoparticles for delivering celastrol, abbreviated as CBR NPs, were constructed to inhibit the infiltration of circulating inflammatory neutrophils (INEs) into inflamed joints while inhibiting the release of NETs to alleviate tissue damage. CBR NPs were prepared for the first time to induce apoptosis of INEs; CBR NPs could inhibit the release of NETs while inducing apoptosis of INEs in vivo and vitro cellular experiments; CBR NPs had favorable anti-inflammatory effects and low toxicity side-effects in collagen-induced arthritis (CIA) mouse models. The application of nanotechnology to induce apoptosis of INEs while inhibiting the release of NETs was a promising approach for the treatment of RA. (c) 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:345 / 357
页数:13
相关论文
共 47 条
[1]   The pathogenesis of rheumatoid arthritis [J].
Alivernini, Stefano ;
Firestein, Gary S. ;
McInnes, Iain B. .
IMMUNITY, 2022, 55 (12) :2255-2270
[2]   The role of neutrophil extracellular traps in rheumatic diseases [J].
Apel, Falko ;
Zychlinsky, Arturo ;
Kenny, Elaine F. .
NATURE REVIEWS RHEUMATOLOGY, 2018, 14 (08) :467-475
[3]   The Neutrophil [J].
Burn, Garth Lawrence ;
Foti, Alessandro ;
Marsman, Gerben ;
Patel, Dhiren Ferise ;
Zychlinsky, Arturo .
IMMUNITY, 2021, 54 (07) :1377-1391
[4]   Neutrophil extracellular traps mediate articular cartilage damage and enhance cartilage component immunogenicity in rheumatoid arthritis [J].
Carmona-Rivera, Carmelo ;
Carlucci, Philip M. ;
Goel, Rishi R. ;
James, Eddie ;
Brooks, Stephen R. ;
Rims, Cliff ;
Hoffmann, Victoria ;
Fox, David A. ;
Buckner, Jane H. ;
Kaplan, Mariana J. .
JCI INSIGHT, 2020, 5 (13)
[5]   Neutrophils and NETs in modulating acute and chronic inflammation [J].
Castanheira, Fernanda V. S. ;
Kubes, Paul .
BLOOD, 2019, 133 (20) :2178-2185
[6]   RGD peptides and monoclonal antibodies, antagonists of αv-integrin, enter the cells by independent endocytic pathways [J].
Castel, S ;
Pagan, R ;
Mitjans, F ;
Piulats, J ;
Goodman, S ;
Jonczyk, A ;
Huber, F ;
Vilaró, S ;
Reina, M .
LABORATORY INVESTIGATION, 2001, 81 (12) :1615-1626
[7]   Celastrol induces ROS-mediated apoptosis via directly targeting peroxiredoxin-2 in gastric cancer cells [J].
Chen, Xi ;
Zhao, Ying ;
Luo, Wu ;
Chen, Sian ;
Lin, Feng ;
Zhang, Xi ;
Fan, Shijie ;
Shen, Xian ;
Wang, Yi ;
Liang, Guang .
THERANOSTICS, 2020, 10 (22) :10290-10308
[8]   Targeted apoptosis of macrophages and osteoclasts in arthritic joints is effective against advanced inflammatory arthritis [J].
Deng, Caifeng ;
Zhang, Quan ;
He, Penghui ;
Zhou, Bin ;
He, Ke ;
Sun, Xun ;
Lei, Guanghua ;
Gong, Tao ;
Zhang, Zhirong .
NATURE COMMUNICATIONS, 2021, 12 (01)
[9]   Current advances in the nano-delivery of celastrol for treating inflammation-associated diseases [J].
Fang, Guihua ;
Tang, Bo .
JOURNAL OF MATERIALS CHEMISTRY B, 2020, 8 (48) :10954-10965
[10]   Global epidemiology of rheumatoid arthritis [J].
Finckh, Axel ;
Gilbert, Benoit ;
Hodkinson, Bridget ;
Bae, Sang-Cheol ;
Thomas, Ranjeny ;
Deane, Kevin D. ;
Alpizar-Rodriguez, Deshire ;
Lauper, Kim .
NATURE REVIEWS RHEUMATOLOGY, 2022, 18 (10) :591-602