Author:
Nakagawa Koji,Yamano Shuji,Nakasaka Hisayo,Hinokio Kenji,Yoshizawa Midori,Aono Toshihiro
Abstract
Parthenogenetic activation with various combinations of the calcium
ionophore A23187 and protein synthesis or phosphorylation inhibitors was
investigated as a means of producing human parthenogenones with one haploid
pronucleus. Unfertilised human aged oocytes exposed to 5 μM A23187 for 5 min
were treated with 10 μg/ml puromycin (puromycin group, 46 oocytes) or
2 mM 6-dimethylaminopurine (DMAP group, 42 oocytes) for 5 h. Oocytes treated
only with A23187 served as a control (control group, 40 oocytes). After
washing the oocytes, they were incubated for up to 37 h. Evidence of
activation (pronuclear formation) and cleavage was observed 18 h and 42 h
after A23187 treatment, respectively. Activation rates in the puromycin and
DMAP groups were significantly higher than in the control group (91% (42/46)
and 77% (34/44) vs 20% (8/40), p < 0.05, respectively). In the
puromycin group, 81% (34/42) of the activated oocytes showed one pronucleus
with the second polar body (2ndPB), whereas none (0/34) of the activated
oocytes in the DMAP group extruded the 2ndPB. The cleavage rate in the
puromycin group was significantly lower than in the DMAP group (38% vs 68%,
p < 0.05). The activated oocytes which had one pronucleus with
the 2ndPB in the puromycin group showed a haploid set of chromosomes
(10/13). In conclusion, the combination of A23187 and puromycin is effective
for producing human parthenogenones with one haploid pronucleus.
Publisher
Cambridge University Press (CUP)
Subject
Cell Biology,Developmental Biology
Cited by
50 articles.
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