Parthenogenetic activation of mouse oocytes following avertin anaesthesia

Development ◽  
1975 ◽  
Vol 33 (4) ◽  
pp. 941-946
Author(s):  
M. H. Kaufman

Avertin anaesthesia induced mouse eggs to become activated parthenogenetically. An increasing incidence of activation was observed when females were anaesthetized 6·5, 9 and 13 h after ovulation, reaching a maximum of 45·8 %. In a spontaneously ovulating group approximately 12·5 % of all the eggs ovulated, or 27·3 % of all the eggs activated evoked a decidual response, and the presence of implanting embryos was confirmed histologically. These findings demonstrate a new and simple method of inducing post-implantation parthenogenetic development in the mouse, and stress the necessity of taking into account the possible consequences of anaesthesia in the early post-ovulatory period.

1997 ◽  
Vol 47 (1) ◽  
pp. 208 ◽  
Author(s):  
Honglin Liu ◽  
Biqin Fan ◽  
Hehai Wang

1992 ◽  
Vol 103 (2) ◽  
pp. 389-396 ◽  
Author(s):  
C. Vincent ◽  
T.R. Cheek ◽  
M.H. Johnson

Nuclear maturation of the mouse oocyte becomes arrested in metaphase of the second meiotic division (MII). Fertilization or parthenogenetic activation induces meiotic completion, chromosomal decondensation and formation of a pronucleus. This completion of meiosis is probably triggered by a transient increase in cytosolic calcium ions. When activated just after ovulation by a low concentration of the calcium ionophore A23187, the majority of the mouse oocytes go through a metaphase to anaphase transition and extrude their second polar body but they do not proceed into interphase; instead their chromatids remain condensed and a microtubular metaphase spindle reforms (metaphase III). However, a high percentage of these oocytes will undergo a true parthenogenetic activation assessed by the formation of a pronucleus, when exposed to a higher concentration of the calcium ionophore. The capacity of the mouse oocyte to pass into metaphase III is lost with increasing time post-ovulation. Direct measurement of intracellular calcium with Fura-2 reveals higher levels of cytosolic calcium in aged oocytes and/or using higher concentrations of calcium ionophore for activation. It is concluded that the internal free calcium level determines the transition to interphase.


Development ◽  
1988 ◽  
Vol 104 (1) ◽  
pp. 97-103 ◽  
Author(s):  
H.J. Clarke ◽  
J. Rossant ◽  
Y. Masui

Mouse oocytes at metaphase I were treated with puromycin, which caused the chromosomes to become decondensed within an interphase nucleus. When the oocytes were allowed to resume protein synthesis, they returned to metaphase within 8–10 h and neither synthesized DNA nor cleaved, indicating that they had not been parthenogenetically activated by the puromycin treatment. However, when dibutyryl cyclic AMP was added to the medium after protein synthesis resumed, the oocytes remained in interphase. These oocytes maintained in interphase began DNA synthesis beginning 20 h after puromycin withdrawal, even though no activation stimulus had been given to them. After transfer to the oviducts of foster mothers, the oocytes could develop to the blastocyst stage. These results indicate that oocytes whose chromosomes were decondensed by puromycin treatment at metaphase I could begin parthenogenetic development in the absence of an activating stimulus, provided that they were prevented from returning to metaphase. In contrast, when the puromycin-treated oocytes were allowed to return to metaphase, they became developmentally arrested at the end of maturation. This suggests that the mechanism responsible for the developmental arrest of mature oocytes at metaphase II depends on cytoplasmic conditions that cause chromosome condensation to the metaphase state.


1995 ◽  
Vol 41 (1) ◽  
pp. 7-14 ◽  
Author(s):  
Hiroshi IMAHIE ◽  
Eimei SATO ◽  
Yutaka TOYODA

2013 ◽  
Vol 17 (3) ◽  
pp. 196-202 ◽  
Author(s):  
Siti Khadijah Idris ◽  
Ramli Bin Abdullah ◽  
Wan Khadijah Wan Embong ◽  
Mohammad Mijanur Rahman

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