Hyaluronic-Acid-Nanomedicine Hydrogel for Enhanced Treatment of Rheumatoid Arthritis by Mediating Macrophage-Synovial Fibroblast Cross-Talk

被引:2
|
作者
Wang, Yaping [1 ]
Wang, Jingrong [2 ]
Ma, Mengze [1 ]
Gao, Rui [2 ]
Wu, Yan [1 ]
Zhang, Chuangnian [2 ]
Huang, Pingsheng [2 ]
Wang, Weiwei [2 ,3 ]
Feng, Zujian [2 ]
Gao, Jianbo [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Med 3D Printing Ctr, Zhengzhou 450000, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Tianjin Key Lab Biomat Res, Inst Biomed Engn, Tianjin 300192, Peoples R China
[3] Chinese Acad Med Sci, Key Lab Innovat Cardiovasc Devices, Beijing 100144, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.34133/bmr.0046
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The occurrence of rheumatoid arthritis (RA) is highly correlated with progressive and irreversible damage of articular cartilage and continuous inflammatory response. Here, inspired by the unique structure of synovial lipid-hyaluronic acid (HA) complex, we developed supramolecular HA-nanomedicine hydrogels for RA treatment by mediating macrophage-synovial fibroblast cross-talk through locally sustained release of celastrol (CEL). Molecular dynamics simulation confirmed that HA conjugated with hydrophobic segments could interspersed into the CEL-loaded [poly(epsilon-caprolactone-co-1,4,8-trioxa[4.6]spiro-9-undecanone)- to form the supramolecular nanomedicine hydrogel HA-poly(epsilon-caprolactone-co-1,4,8-trioxa[4.6]spiro-9un-decanone)/PECT@CEL (HP@CEL), enabling fast hydrogel formation after injection and providing a 3-dimensional environment similar with synovial region. More importantly, the controlled release of CEL from HP@CEL inhibited the macrophage polarization toward the proinflammatory M1 phenotype and further suppressed the proliferation of synovial fibroblasts by regulating the Toll-like receptor pathway. In collagen-induced arthritis model in mice, HP@CEL hydrogel treatment substantial attenuated clinical symptoms and bone erosion and improved the extracellular matrix deposition and bone regeneration in ankle joint. Altogether, such a bioinspired injectable polymer-nanomedicine hydrogel represents an effective and promising strategy for suppressing RA progression through augmenting the cross-talk of macrophages and synovial fibroblast for regulation of chronic inflammation.
引用
收藏
页数:14
相关论文
共 17 条
  • [1] How Pyroptosis Contributes to Inflammation and Fibroblast-Macrophage Cross-Talk in Rheumatoid Arthritis
    Demarco, Benjamin
    Danielli, Sara
    Fischer, Fabian A.
    Bezbradica, Jelena S.
    CELLS, 2022, 11 (08)
  • [2] Cytokine-directed cellular cross-talk imprints synovial pathotypes in rheumatoid arthritis
    Kugler, Maximilian
    Dellinger, Mirjam
    Kartnig, Felix
    Mueller, Lena
    Preglej, Teresa
    Heinz, Leonhard X.
    Simader, Elisabeth
    Goeschl, Lisa
    Puchner, Stephan E.
    Weiss, Sebastian
    Shaw, Lisa E.
    Farlik, Matthias
    Weninger, Wolfgang
    Superti-Furga, Giulio
    Smolen, Josef S.
    Steiner, Guenter
    Aletaha, Daniel
    Kiener, Hans P.
    Lewis, Myles J.
    Pitzalis, Costantino
    Tosevska, Anela
    Karonitsch, Thomas
    Bonelli, Michael
    ANNALS OF THE RHEUMATIC DISEASES, 2023, 82 (09) : 1142 - 1152
  • [3] IL-15 and the initiation of cell contact-dependent synovial fibroblast-T lymphocyte cross-talk in rheumatoid arthritis:: Effect of methotrexate
    Miranda-Carús, ME
    Balsa, A
    Benito-Miguel, M
    de Ayala, CP
    Martín-Mola, E
    JOURNAL OF IMMUNOLOGY, 2004, 173 (02): : 1463 - 1476
  • [4] Coordinating Macrophage Targeting and Antioxidation by Injectable Nanocomposite Hydrogel for Enhanced Rheumatoid Arthritis Treatment
    Liu, Houqin
    Liu, Yingke
    Tian, Zhipeng
    Li, Jiaxin
    Li, Man
    Zhao, Zhihe
    ACS APPLIED MATERIALS & INTERFACES, 2024, 16 (29) : 37656 - 37668
  • [5] IL-6 secretion in osteoarthritis patients is mediated by chondrocyte-synovial fibroblast cross-talk and is enhanced by obesity
    Mark J. Pearson
    Dietmar Herndler-Brandstetter
    Mohammad A. Tariq
    Thomas A. Nicholson
    Ashleigh M. Philp
    Hannah L. Smith
    Edward T. Davis
    Simon W. Jones
    Janet M. Lord
    Scientific Reports, 7
  • [6] IL-6 secretion in osteoarthritis patients is mediated by chondrocyte-synovial fibroblast cross-talk and is enhanced by obesity
    Pearson, Mark J.
    Herndler-Brandstetter, Dietmar
    Tariq, Mohammad A.
    Nicholson, Thomas A.
    Philp, Ashleigh M.
    Smith, Hannah L.
    Davis, Edward T.
    Jones, Simon W.
    Lord, Janet M.
    SCIENTIFIC REPORTS, 2017, 7
  • [7] Cross-talk between IL-1 and IL-6 signaling pathways in rheumatoid arthritis synovial fibroblasts
    Deon, D
    Ahmed, S
    Tai, K
    Scaletta, N
    Herrero, C
    Lee, IH
    Krause, A
    Ivashkiv, LB
    JOURNAL OF IMMUNOLOGY, 2001, 167 (09): : 5395 - 5403
  • [8] Cross-talk between polymorphonuclear neutrophils (PMN) and T-cells at the site of inflammation in the synovial fluid in rheumatoid arthritis (RA)
    Iking-Konert, C
    Ostendorf, B
    Sander, O
    Jost, M
    Joosten, L
    Schneider, M
    Haensch, M
    ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 : 133 - 133
  • [9] Cross-talk between synovial fibroblasts (SFiB) and T lymphocytes (TL) in the pathogenesis of rheumatoid arthritis (RA): Effect of methotrexate (MTX)
    Miranda, E
    Balsa, A
    Benito, M
    De Cozar, C
    Pascual-Salcedo, D
    Martin-Mola, E
    ANNALS OF THE RHEUMATIC DISEASES, 2003, 62 : 137 - 137
  • [10] Cross-talk between synovial fibroblasts (SFib) and T lymphocytes (TL) in the pathogenesis of rheumatoid arthritis (RA):: Effect of methotrexate.
    Miranda, E
    Balsa, A
    Pascual-Salcedo, D
    Sánchez, M
    Gómez, L
    Sánchez-Mateos, P
    Martin-Mola, E
    ARTHRITIS AND RHEUMATISM, 2002, 46 (09): : S200 - S201