Pregled bibliografske jedinice broj: 208171
Phytohaemagglutinin as a modulator of chromosomal aberration assay and micronucleus assay in ionizing radiation biodosimetry
Phytohaemagglutinin as a modulator of chromosomal aberration assay and micronucleus assay in ionizing radiation biodosimetry // Book of abstarcts of the second congress of Croatian geneticists / Franekić Ćolić, Jasna ; Ugarković, Đurđica (ur.).
Zagreb: itg DIGITALNI TISAK, 2005. (predavanje, međunarodna recenzija, pp prezentacija, znanstveni)
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Naslov
Phytohaemagglutinin as a modulator of chromosomal aberration assay and micronucleus assay in ionizing radiation biodosimetry
Autori
Đurinec, Martina ; Želježić, Davor ; Garaj-Vrhovac, Verica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, pp prezentacija, znanstveni
Izvornik
Book of abstarcts of the second congress of Croatian geneticists
/ Franekić Ćolić, Jasna ; Ugarković, Đurđica - Zagreb : Itg DIGITALNI TISAK, 2005
Skup
Second congress of Croatian geneticists
Mjesto i datum
Brač, Hrvatska, 24.09.2005. - 27.09.2005
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Ionizing radiation; Phytohaemagglutinin; Chromosome aberration; Micronucleus assay
Sažetak
For more than 30 years chromosomal aberration analysis and micronucleus assay have been considered to be important cytogenetical tool in biological effects evaluation of ionizing radiation. To make the radiation-caused DNA damage visible, cells have to be initiated to enter the G1 phase, to pass the S phase of the cycle.Therefore the cultivation of peripheral blood lymphocytes in the presence of mitogen activator is required. The mostly used is phytohaemagglutinin. We intended to find out whether the point when the phytohaemagglutinin is added after the culture initiation has any influence on chromosomal aberration and micronuclei formation. Human peripheral blood lymphocytes were isolated. To initiate DNA damage lymphocytes were irradiated by 2 Gy using a gamma-ray 60 Co source. The cultures for chromosomal aberration analysis and micronucleus assay were started and phytohaemagglutinin was added 0, 1, 2 or 4 hours after irradiation. The number of dicentric chromosomes and acentric fragments were significantly increased in lymphocytes stimulated by phytohaemagglutinin immmediately after irradiation compared to the cultures where activator after 1, 2 and 4 hours was added. The number of aberrations between activator after 1, 2 and 4 hours after irradiation did not differ significantly. Micronucleus assay did not show any significant differences in number of micronuclei regardless of the time when the mitogen activator was added. We could say that in order to maximize the sensitivity of chromosomal aberration analysis phytohaemagglutinin has to be added immediately after the irradiation.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
0022020
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb