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Naslov:HepG2 spheroids as a biosensor-like cell-based system for (geno)toxicity assessment
Avtorji:ID Štampar, Martina (Avtor)
ID Žabkar, Sonja (Avtor)
ID Filipič, Metka (Avtor)
ID Žegura, Bojana (Avtor)
Datoteke:URL URL - Izvorni URL, za dostop obiščite https://www.sciencedirect.com/science/article/pii/S004565352103277X#!
 
.pdf PDF - Predstavitvena datoteka, prenos (6,21 MB)
MD5: A287AADEF5CEBA4DD1C09DF2B71BEF9C
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo NIB - Nacionalni inštitut za biologijo
Povzetek:3D spheroids developed from HepG2 cells were used as a biosensor-like system for the detection of (geno)toxic effects induced by chemicals. Benzo(a)pyrene (B(a)P) and amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with well-known mechanisms of action were used for system validation. HepG2 spheroids grown for 3 days were exposed to BaP and PhIP for 24 and 72 h. The growth and viability of spheroids were monitored by planimetry and Live/Dead staining of cells. Multi-parametric flow cytometric analysis was applied for simultaneous detection of specific end-effects including cell cycle analysis (Hoechst staining), cell proliferation (KI67 marker), and DNA double-strand breaks (ℽH2AX) induced by genotoxic compounds. Depending on the exposure concentration/time, BaP reduced spheroid growth, affected cell proliferation by arresting cells in S and G2 phase and induced DNA double-strand breaks (DSB). Simultaneous staining of ℽH2AX formation and cell cycle analysis revealed that after BaP (10 μM; 24 h) exposure 60% of cells in G0/G1 phase had DNA DSB, while after 72 h only 20% of cells contained DSB indicating efficient repair of DNA lesions. PhIP did not influence the spheroid size whereas accumulation of cells in the G2 phase occurred after both treatment times. The evaluation of DNA damage revealed that at 200 μM PhIP 50% of cells in G0/G1 phase had DNA DSB, which after 72-h exposure dropped to 40%, showing lower repair capacity of PhIP-induced DSB compared to BaP-induced. The developed approach using simultaneous detection of several parameters provides mechanistic data and thus contributes to more reliable genotoxicity assessment of chemicals as a high-content screening tool.
Ključne besede:in vitro 3D cell model, HepG2, flow cytometry, cell cycle, proliferation, DNA strand, breaks
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:01.03.2022
Leto izida:2022
Št. strani:str. 1-11
Številčenje:Vol. 291, pt. 1
PID:20.500.12556/DiRROS-19310 Novo okno
UDK:577
ISSN pri članku:0045-6535
DOI:10.1016/j.chemosphere.2021.132805 Novo okno
COBISS.SI-ID:84412419 Novo okno
Opomba:Št. članka: 132805;
Datum objave v DiRROS:16.07.2024
Število ogledov:330
Število prenosov:185
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Chemosphere
Skrajšan naslov:Chemosphere
Založnik:Pergamon Press.
ISSN:0045-6535
COBISS.SI-ID:25213696 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P1-0245-2019
Naslov:Ekotoksiologija, toksikološka genomika in karcinogeneza

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:J1-2465-2020
Naslov:Napredni 3D celični modeli: Premostitev vrzeli med in vitro in in vivo poskusnimi sistemi (hep3DGenTox)

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:biokemija, celični model in vitro 3D, HepG2, celični cikel


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