Počet záznamů: 1  

Nanoparticle core stability and surface functionalization drive the mTOR signaling pathway in hepatocellular cell lines.

  1. 1.
    SYSNO ASEP0482038
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevNanoparticle core stability and surface functionalization drive the mTOR signaling pathway in hepatocellular cell lines.
    Tvůrce(i) Lunova, M. (CZ)
    Prokhorov, A. (CZ)
    Jirsa, M. (CZ)
    Hof, M. (CZ)
    Olžyńska, A. (CZ)
    Jurkiewicz, P. (CZ)
    Kubinová, Šárka (UEM-P) RID, ORCID
    Lunov, O. (CZ)
    Dejneka, A. (CZ)
    Zdroj.dok.Scientific Reports. - : Nature Publishing Group - ISSN 2045-2322
    Roč. 7, č. 1 (2017), s. 16049
    Poč.str.16 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovamesoporous silica nanoparticles ; iron-oxide nanoparticles ; double-stranded-rna ; drug-delivery
    Vědní obor RIVFP - Ostatní lékařské obory
    Obor OECDBiophysics
    CEPLO1309 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaUEM-P - RVO:68378041
    UT WOS000416118900015
    EID SCOPUS85034824356
    DOI https://doi.org/10.1038/s41598-017-16447-6
    AnotaceSpecifically designed and functionalized nanoparticles hold great promise for biomedical applications. Yet, the applicability of nanoparticles is critically predetermined by their surface functionalization and biodegradability. Here we demonstrate that amino-functionalized polystyrene nanoparticles (PS-NH2), but not amino-or hydroxyl-functionalized silica particles, trigger cell death in hepatocellular carcinoma Huh7 cells. Importantly, biodegradability of nanoparticles plays a crucial role in regulation of essential cellular processes. Thus, biodegradable silica nanoparticles having the same shape, size and surface functionalization showed opposite cellular effects in comparison with similar polystyrene nanoparticles. At the molecular level, PS-NH2 obstruct and amino-functionalized silica nanoparticles (Si-NH2) activate the mTOR signalling in Huh7 and HepG2 cells. PS-NH2 induced time-dependent lysosomal destabilization associated with damage of the mitochondrial membrane. Solely in PS-NH2-treated cells, permeabilization of lysosomes preceded cell death. Contrary, Si-NH2 nanoparticles enhanced proliferation of HuH7 and HepG2 cells. Our findings demonstrate complex cellular responses to functionalized nanoparticles and suggest that nanoparticles can be used to control activation of mTOR signaling with subsequent influence on proliferation and viability of HuH7 cells. The data provide fundamental knowledge which could help in developing safe and efficient nano-therapeutics.
    PracovištěÚstav experimentální medicíny
    KontaktArzuv Čaryjeva, arzuv.caryjeva@iem.cas.cz, Tel.: 241 062 218, 296 442 218
    Rok sběru2018
Počet záznamů: 1  

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