Influence of proliferation on DNA repair rates in liver

To test the hypothesis that the proliferative status of a mammalian cell determines the rate of removal of oxidative DNA damage, pre- and posthepatectomized livers in adult male Fisher 344 rats were irradiated in situ with 15.5 Gy of 137Cs γ-rays. At 10 and 45 min after irradiation, the livers were...

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Veröffentlicht in:Experimental cell research 1991-12, Vol.197 (2), p.323-325
Hauptverfasser: Clair, William H.St, Dwarakanath, B.S., Zhang, Hong, Wheeler, Kenneth T.
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Dwarakanath, B.S.
Zhang, Hong
Wheeler, Kenneth T.
description To test the hypothesis that the proliferative status of a mammalian cell determines the rate of removal of oxidative DNA damage, pre- and posthepatectomized livers in adult male Fisher 344 rats were irradiated in situ with 15.5 Gy of 137Cs γ-rays. At 10 and 45 min after irradiation, the livers were removed and dissociated into single cell suspensions, and the DNA damage in the isolated quiescent or proliferative liver cells was assayed by alkaline elution. Proliferative liver cells irradiated 20–24 h or 29–31 h after hepatectomy repaired their DNA damage faster than quiescent liver cells. A corresponding increase in the accessibility of the DNA to digestion by m. nuclease was observed for the posthepatectomized liver cells. These data suggest that proliferative status is a major determinant of the rate of DNA repair in rat liver.
doi_str_mv 10.1016/0014-4827(91)90440-6
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At 10 and 45 min after irradiation, the livers were removed and dissociated into single cell suspensions, and the DNA damage in the isolated quiescent or proliferative liver cells was assayed by alkaline elution. Proliferative liver cells irradiated 20–24 h or 29–31 h after hepatectomy repaired their DNA damage faster than quiescent liver cells. A corresponding increase in the accessibility of the DNA to digestion by m. nuclease was observed for the posthepatectomized liver cells. These data suggest that proliferative status is a major determinant of the rate of DNA repair in rat liver.</abstract><cop>Orlando, FL</cop><pub>Elsevier Inc</pub><pmid>1959564</pmid><doi>10.1016/0014-4827(91)90440-6</doi><tpages>3</tpages></addata></record>
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subjects 560120 - Radiation Effects on Biochemicals, Cells, & Tissue Culture
ALKALI METAL ISOTOPES
ANIMAL CELLS
ANIMALS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
Biological and medical sciences
BIOLOGICAL EFFECTS
BIOLOGICAL RADIATION EFFECTS
BIOLOGICAL RECOVERY
BIOLOGICAL REPAIR
Cell Division
CELL PROLIFERATION
Cells, Cultured
CESIUM 137
CESIUM ISOTOPES
DNA
DNA - genetics
DNA - isolation & purification
DNA Damage
DNA REPAIR
ELECTROMAGNETIC RADIATION
Fundamental and applied biological sciences. Psychology
GAMMA RADIATION
Hepatectomy
INTERMEDIATE MASS NUCLEI
IONIZING RADIATIONS
ISOTOPES
Kinetics
Liver - cytology
Liver - physiology
LIVER CELLS
Male
MALES
MAMMALS
Molecular and cellular biology
MOLECULAR BIOLOGY
Molecular genetics
Mutagenesis. Repair
NUCLEI
NUCLEIC ACIDS
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
RADIATION EFFECTS
RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT
RADIATIONS
RADIOISOTOPES
RATS
Rats, Inbred F344
REPAIR
RODENTS
SOMATIC CELLS
Time Factors
VERTEBRATES
YEARS LIVING RADIOISOTOPES
title Influence of proliferation on DNA repair rates in liver
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