TY - JOUR
T1 - Terminal differentiation of human erythroleukemia cell line K562 induced by aphidicolin
AU - Murate, Takashi
AU - Kagami, Yoshitoyo
AU - Hotta, Tomomitsu
AU - Yoshida, Tomoaki
AU - Saito, Hidehiko
AU - Yoshida, Shonen
N1 - Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 1990/11
Y1 - 1990/11
N2 - To analyze the relationship between differentiation and DNA replication, the effect of aphidicolin, a specific inhibitor for DNA polymerase α, was measured with respect to erythroid differentiation and activities of DNA polymerases α,β, and γ. Five micromolar aphidicolin completely blocked the growth of K562 cells and caused 80% of cells to become hemoglobin positive after 5 days exposure. The cessation of K562 cell growth induced by aphidicolin was irreversible, whereas the inhibition of HeLa cell growth was completely reversible. The enzyme activity of DNA polymerase α of K562 cells showed a 50-110% increase with aphidicolin treatment as compared to control K562 cells; activities of DNA polymerases β and γ were not affected. These features sharply contrasted with the erythroid induction of the same cells by hemin, where cell growth was not suppressed and DNA polymerase α was not increased but rather decreased. The enzyme activity of DNA polymerase α remained high even after removal of aphidicolin from the culture medium. These results suggest that treatment with aphidicolin might induce an accumulation of protein factors for replication and/or differentiation, causing rapid cell differentiation of cells without Cell division.
AB - To analyze the relationship between differentiation and DNA replication, the effect of aphidicolin, a specific inhibitor for DNA polymerase α, was measured with respect to erythroid differentiation and activities of DNA polymerases α,β, and γ. Five micromolar aphidicolin completely blocked the growth of K562 cells and caused 80% of cells to become hemoglobin positive after 5 days exposure. The cessation of K562 cell growth induced by aphidicolin was irreversible, whereas the inhibition of HeLa cell growth was completely reversible. The enzyme activity of DNA polymerase α of K562 cells showed a 50-110% increase with aphidicolin treatment as compared to control K562 cells; activities of DNA polymerases β and γ were not affected. These features sharply contrasted with the erythroid induction of the same cells by hemin, where cell growth was not suppressed and DNA polymerase α was not increased but rather decreased. The enzyme activity of DNA polymerase α remained high even after removal of aphidicolin from the culture medium. These results suggest that treatment with aphidicolin might induce an accumulation of protein factors for replication and/or differentiation, causing rapid cell differentiation of cells without Cell division.
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U2 - 10.1016/0014-4827(90)90033-7
DO - 10.1016/0014-4827(90)90033-7
M3 - Article
C2 - 2121512
AN - SCOPUS:0025037144
SN - 0014-4827
VL - 191
SP - 45
EP - 50
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 1
ER -