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Metal Nanoparticles with Antimicrobial Properties: The Toxicity Response in Mouse Mesenchymal Stem Cells

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    SYSNO ASEP0581955
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMetal Nanoparticles with Antimicrobial Properties: The Toxicity Response in Mouse Mesenchymal Stem Cells
    Author(s) Rössner ml., Pavel (UEM-P) RID, ORCID
    Červená, Tereza (UEM-P) ORCID, RID
    Echalar, Barbora (UEM-P)
    Palacká, Kateřina (UEM-P) ORCID
    Milcová, Alena (UEM-P)
    Novaková, Zuzana (UEM-P)
    Šíma, Michal (UEM-P) RID, ORCID
    Šímová, Zuzana (UEM-P) ORCID
    Vaňková, Jolana (UEM-P)
    Holáň, Vladimír (UEM-P) RID
    Article number253
    Source TitleToxics. - : MDPI
    Roč. 11, č. 3 (2023)
    Number of pages21 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsmetal nanoparticles ; antimicrobial properties ; mesenchymal stem cells ; toxicity
    OECD categoryPublic and environmental health
    R&D ProjectsGA21-17720S GA ČR - Czech Science Foundation (CSF)
    LM2018133 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    EF16_013/0001821 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LM2018124 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUEM-P - RVO:68378041
    UT WOS000959873500001
    EID SCOPUS85151149941
    DOI10.3390/toxics11030253
    AnnotationSome metal nanoparticles (NP) are characterized by antimicrobial properties with the potential to be used as alternative antibiotics. However, NP may negatively impact human organism, including mesenchymal stem cells (MSC), a cell population contributing to tissue growth and regeneration. To address these issues, we investigated the toxic effects of selected NP (Ag, ZnO, and CuO) in mouse MSC. MSC were treated with various doses of NP for 4 h, 24 h, and 48 h and multiple endpoints were analyzed. Reactive oxygen species were generated after 48 h CuO NP exposure. Lipid peroxidation was induced after 4 h and 24 h treatment, regardless of NP and/or tested dose. DNA fragmentation and oxidation induced by Ag NP showed dose responses for all the periods. For other NP, the effects were observed for shorter exposure times. The impact on the frequency of micronuclei was weak. All the tested NP increased the sensitivity of MSC to apoptosis. The cell cycle was most affected after 24 h, particularly for Ag NP treatment. In summary, the tested NP induced numerous adverse changes in MSC. These results should be taken into consideration when planning the use of NP in medical applications where MSC are involved.
    WorkplaceInstitute of Experimental Medicine
    ContactLenka Koželská, lenka.kozelska@iem.cas.cz, Tel.: 241 062 218, 296 442 218
    Year of Publishing2024
    Electronic addresshttps://www.mdpi.com/2305-6304/11/3/253
Number of the records: 1  

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