Počet záznamů: 1  

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

  1. 1.
    0482038 - ÚEM 2018 RIV GB eng J - Článek v odborném periodiku
    Lunova, M. - Prokhorov, A. - Jirsa, M. - Hof, M. - Olžyńska, A. - Jurkiewicz, P. - Kubinová, Šárka - Lunov, O. - Dejneka, A.
    Nanoparticle core stability and surface functionalization drive the mTOR signaling pathway in hepatocellular cell lines.
    Scientific Reports. Roč. 7, č. 1 (2017), s. 16049. ISSN 2045-2322. E-ISSN 2045-2322
    Grant CEP: GA MŠMT(CZ) LO1309
    Institucionální podpora: RVO:68378041
    Klíčová slova: mesoporous silica nanoparticles * iron-oxide nanoparticles * double-stranded-rna * drug-delivery
    Obor OECD: Biophysics
    Impakt faktor: 4.122, rok: 2017

    Specifically 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.
    Trvalý link: http://hdl.handle.net/11104/0281277

     
     
Počet záznamů: 1  

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