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Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis

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    0599455 - FGÚ 2025 RIV US eng J - Journal Article
    Doubková, Martina - Knitlová, Jarmila - Vondrášek, David - Eckhardt, Adam - Novotný, T. - Ošťádal, M. - Filová, Elena - Bačáková, Lucie
    Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis.
    Biomacromolecules. Roč. 25, č. 10 (2024), s. 6485-6502. ISSN 1525-7797. E-ISSN 1526-4602
    R&D Projects: GA MZd(CZ) NU22-10-00072; GA MŠMT(CZ) EH22_008/0004562; GA MŠMT(CZ) EF18_046/0016045
    Grant - others:AV ČR(CZ) AP2202
    Program: Akademická prémie - Praemium Academiae
    Research Infrastructure: Czech-BioImaging III - 90250
    Institutional support: RVO:67985823
    Keywords : clubfoot * fibrosis * cell culture * biopolymers
    OECD category: Orthopaedics
    Impact factor: 5.5, year: 2023 ; AIS: 1.018, rok: 2023
    Method of publishing: Open access
    Result website:
    https://doi.org/10.1021/acs.biomac.4c00653DOI: https://doi.org/10.1021/acs.biomac.4c00653

    Fibrotic changes in pediatric clubfoot provide an opportunity to improve corrective therapy and prevent relapses with targeted drugs. This study defines the parameters of clubfoot fibrosis and presents a unique analysis of a simple pseudo-3D in vitro model for disease-specific high-throughput drug screening experiments. The model combines clubfoot-derived fibroblasts with a biomimetic cultivation environment induced by the water-soluble polymers Ficoll and Polyvinylpyrrolidone, utilizing the principle of macromolecular crowding. We achieved higher conversion of soluble collagen into insoluble collagen, accelerated formation of the extracellular matrix layer and upregulated fibrosis-related genes in the mixed Ficoll environment. To test the model, we evaluated the effect of a potential antifibrotic drug, minoxidil, emphasizing collagen content and cross-linking. While the model amplified overall collagen deposition, minoxidil effectively blocked the expression of lysyl hydroxylases, which are responsible for the increased occurrence of specific collagen cross-linking in various fibrotic tissues. This limited the formation of collagen cross-link in both the model and control environments. Our findings provide a tool for expanding preclinical research for clubfoot and similar fibroproliferative conditions.
    Permanent Link: https://hdl.handle.net/11104/0356881


     
     
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Number of the records: 1  

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