-
Je něco špatně v tomto záznamu ?
Nonhomologous DNA end joining and chromosome aberrations in human embryonic lung fibroblasts treated with environmental pollutants
P. Rossner, A. Rossnerova, O. Beskid, N. Tabashidze, H. Libalova, K. Uhlirova, J. Topinka, RJ. Sram,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- antigeny jaderné genetika metabolismus MeSH
- benzopyren toxicita MeSH
- buněčné linie MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- embryo savčí metabolismus patologie MeSH
- fibroblasty metabolismus patologie MeSH
- fosforylace účinky léků genetika MeSH
- histony genetika metabolismus MeSH
- látky znečišťující životní prostředí toxicita MeSH
- lidé MeSH
- lidské chromozomy genetika metabolismus MeSH
- obnova měst MeSH
- oprava DNA spojením konců účinky léků genetika MeSH
- pevné částice MeSH
- plíce metabolismus patologie MeSH
- translokace genetická účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
In order to evaluate the ability of a representative polycyclic aromatic hydrocarbon (PAH) and PAH-containing complex mixtures to induce double strand DNA breaks (DSBs) and repair of damaged DNA in human embryonic lung fibroblasts (HEL12469 cells), we investigated the effect of benzo[a]pyrene (B[a]P) and extractable organic matter (EOM) from ambient air particles <2.5μm (PM2.5) on nonhomologous DNA end joining (NHEJ) and induction of stable chromosome aberrations (CAs). PM2.5 was collected in winter and summer 2011 in two Czech cities differing in levels and sources of air pollutants. The cells were treated for 24h with the following concentrations of tested chemicals: B[a]P: 1μM, 10μM, 25μM; EOMs: 1μg/ml, 10μg/ml, 25μg/ml. We tested several endpoints representing key steps leading from DSBs to the formation of CAs including histone H2AX phosphorylation, levels of proteins Ku70, Ku80 and XRCC4 participating in NHEJ, in vitro ligation activity of nuclear extracts of the HEL12469 cells and the frequency of stable CAs assessed by whole chromosome painting of chromosomes 1, 2, 4, 5, 7 and 17 using fluorescence in situ hybridization. Our results show that 25μM of B[a]P and most of the tested doses of EOMs induced DSBs as indicated by H2AX phosphorylation. DNA damage was accompanied by induction of XRCC4 expression and an increased frequency of CAs. Translocations most frequently affected chromosome 7. We observed only a weak induction of Ku70/80 expression as well as ligation activity of nuclear extracts. In summary, our data suggest the induction of DSBs and NHEJ after treatment of human embryonic lung fibroblasts with B[a]P and complex mixtures containing PAHs.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15023505
- 003
- CZ-PrNML
- 005
- 20150727124325.0
- 007
- ta
- 008
- 150709s2014 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.mrfmmm.2014.03.006 $2 doi
- 035 __
- $a (PubMed)24694657
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Rossner, Pavel $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic. Electronic address: prossner@biomed.cas.cz.
- 245 10
- $a Nonhomologous DNA end joining and chromosome aberrations in human embryonic lung fibroblasts treated with environmental pollutants / $c P. Rossner, A. Rossnerova, O. Beskid, N. Tabashidze, H. Libalova, K. Uhlirova, J. Topinka, RJ. Sram,
- 520 9_
- $a In order to evaluate the ability of a representative polycyclic aromatic hydrocarbon (PAH) and PAH-containing complex mixtures to induce double strand DNA breaks (DSBs) and repair of damaged DNA in human embryonic lung fibroblasts (HEL12469 cells), we investigated the effect of benzo[a]pyrene (B[a]P) and extractable organic matter (EOM) from ambient air particles <2.5μm (PM2.5) on nonhomologous DNA end joining (NHEJ) and induction of stable chromosome aberrations (CAs). PM2.5 was collected in winter and summer 2011 in two Czech cities differing in levels and sources of air pollutants. The cells were treated for 24h with the following concentrations of tested chemicals: B[a]P: 1μM, 10μM, 25μM; EOMs: 1μg/ml, 10μg/ml, 25μg/ml. We tested several endpoints representing key steps leading from DSBs to the formation of CAs including histone H2AX phosphorylation, levels of proteins Ku70, Ku80 and XRCC4 participating in NHEJ, in vitro ligation activity of nuclear extracts of the HEL12469 cells and the frequency of stable CAs assessed by whole chromosome painting of chromosomes 1, 2, 4, 5, 7 and 17 using fluorescence in situ hybridization. Our results show that 25μM of B[a]P and most of the tested doses of EOMs induced DSBs as indicated by H2AX phosphorylation. DNA damage was accompanied by induction of XRCC4 expression and an increased frequency of CAs. Translocations most frequently affected chromosome 7. We observed only a weak induction of Ku70/80 expression as well as ligation activity of nuclear extracts. In summary, our data suggest the induction of DSBs and NHEJ after treatment of human embryonic lung fibroblasts with B[a]P and complex mixtures containing PAHs.
- 650 _2
- $a antigeny jaderné $x genetika $x metabolismus $7 D034961
- 650 _2
- $a benzopyren $x toxicita $7 D001564
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a lidské chromozomy $x genetika $x metabolismus $7 D002877
- 650 _2
- $a oprava DNA spojením konců $x účinky léků $x genetika $7 D059766
- 650 _2
- $a DNA vazebné proteiny $x genetika $x metabolismus $7 D004268
- 650 _2
- $a embryo savčí $x metabolismus $x patologie $7 D004622
- 650 _2
- $a látky znečišťující životní prostředí $x toxicita $7 D004785
- 650 _2
- $a fibroblasty $x metabolismus $x patologie $7 D005347
- 650 _2
- $a histony $x genetika $x metabolismus $7 D006657
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a plíce $x metabolismus $x patologie $7 D008168
- 650 _2
- $a pevné částice $7 D052638
- 650 _2
- $a fosforylace $x účinky léků $x genetika $7 D010766
- 650 _2
- $a translokace genetická $x účinky léků $7 D014178
- 650 _2
- $a obnova měst $7 D014506
- 651 _2
- $a Česká republika $7 D018153
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Rossnerova, Andrea $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Beskid, Olena $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Tabashidze, Nana $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Libalova, Helena $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Uhlirova, Katerina $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Topinka, Jan $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 700 1_
- $a Sram, Radim J $u Department of Genetic Ecotoxicology, Institute of Experimental Medicine AS CR, Prague, Czech Republic.
- 773 0_
- $w MED00003430 $t Mutation research $x 1873-135X $g Roč. 763-764, č. - (2014), s. 28-38
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24694657 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150709 $b ABA008
- 991 __
- $a 20150727124409 $b ABA008
- 999 __
- $a ok $b bmc $g 1083842 $s 906498
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 763-764 $c - $d 28-38 $i 1873-135X $m Mutation research $n Mutat Res $x MED00003430
- LZP __
- $a Pubmed-20150709