RÖSSNER, Pavel, Kristýna VRBOVÁ, Simona STRAPÁČOVÁ, Andrea ROSSNEROVÁ, Antonin AMBROZ, Tana BRZICOVA, Helena LIBALOVÁ, Eliška JAVORKOVÁ, Pavel KULICH, Zbyněk VEČEŘA, Pavel MIKUŠKA, Pavel COUFALÍK, Kamil KRUMAL, Lukáš ČAPKA, Bohumil DOČEKAL, Pavel MORAVEC, Omar ŠERÝ, Ivan MÍŠEK, Petr FICTUM, Karel FIŠER, Miroslav MACHALA a Jan TOPINKA. Inhalation of ZnO Nanoparticles: Splice Junction Expression and Alternative Splicing in Mice. Toxicological sciences. Academic Press, 2019, roč. 168, č. 1, s. 190-200. ISSN 1096-6080. Dostupné z: https://dx.doi.org/10.1093/toxsci/kfy288.
Další formáty:   BibTeX LaTeX RIS
Základní údaje
Originální název Inhalation of ZnO Nanoparticles: Splice Junction Expression and Alternative Splicing in Mice
Autoři RÖSSNER, Pavel, Kristýna VRBOVÁ, Simona STRAPÁČOVÁ, Andrea ROSSNEROVÁ, Antonin AMBROZ, Tana BRZICOVA, Helena LIBALOVÁ, Eliška JAVORKOVÁ, Pavel KULICH, Zbyněk VEČEŘA, Pavel MIKUŠKA, Pavel COUFALÍK, Kamil KRUMAL, Lukáš ČAPKA, Bohumil DOČEKAL, Pavel MORAVEC, Omar ŠERÝ, Ivan MÍŠEK, Petr FICTUM, Karel FIŠER, Miroslav MACHALA a Jan TOPINKA.
Vydání Toxicological sciences, Academic Press, 2019, 1096-6080.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30108 Toxicology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 3.703
Organizační jednotka Přírodovědecká fakulta
Doi http://dx.doi.org/10.1093/toxsci/kfy288
UT WoS 000462865100017
Klíčová slova česky nanočástice; myš; inhalace
Klíčová slova anglicky nanoparticles; mice; inhalation
Štítky RIV ne
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Marie Šípková, DiS., učo 437722. Změněno: 12. 5. 2021 12:48.
Anotace
Despite the wide application of nanomaterials, toxicity studies of nanoparticles (NP) are often limited to in vitro cell models, and the biological impact of NP exposure in mammals has not been thoroughly investigated. Zinc oxide (ZnO) NPs are commonly used in various consumer products. To evaluate the effects of the inhalation of ZnO NP in mice, we studied splice junction expression in the lungs as a proxy to gene expression changes analysis. Female ICR mice were treated with 6.46 * 104 and 1.93 * 106 NP/cm3 for 3 days and 3 months, respectively. An analysis of differential expression and alternative splicing events in 298 targets (splice junctions) of 68 genes involved in the processes relevant to the biological effects of ZnO NP was conducted using next-generation sequencing. Three days of exposure resulted in the upregulation of IL-6 and downregulation of BID, GSR, NF-kB2, PTGS2, SLC11A2, and TXNRD1 splice junction expression; 3 months of exposure increased the expression of splice junctions in ALDH3A1, APAF1, BID, CASP3, DHCR7, GCLC, GCLM, GSR, GSS, EHHADH, FAS, HMOX-1, IFNgamma, NF-kB1, NQO-1, PTGS1, PTGS2, RAD51, RIPK2, SRXN1, TRAF6, and TXNRD1. Alternative splicing of TRAF6 and TXNRD1 was induced after 3 days of exposure to 1.93 * 106 NP/cm3. In summary, we observed changes of splice junction expression in genes involved in oxidative stress, apoptosis, immune response, inflammation, and DNA repair, as well as the induction of alternative splicing in genes associated with oxidative stress and inflammation. Our data indicate the potential negative biological effects of ZnO NP inhalation.
VytisknoutZobrazeno: 18. 7. 2024 05:43