• 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,

. 2014 ; 763-764 (-) : 28-38.

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc15023505

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

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...