Vs. Marshall et al., Parthenogenetic activation of marmoset (Callithrix jacchus) oocytes and the development of marmoset parthenogenones in vitro and in vivo, BIOL REPROD, 59(6), 1998, pp. 1491-1497
Mammalian oocytes can be induced to resume meiosis without fertilization, a
nd the resulting parthenogenetic embryos carry only maternal chromosomes. H
uman oocytes can be activated by many chemical and physical stimuli, but po
stimplantation studies of human parthenogenetic embryos are not ethically a
cceptable. The common marmoset monkey (Callithrix jacchus) is a good model
for studying primate parthenogenetic development postimplantation, since fo
llicular aspiration, embryo transfer, and early postimplantation developmen
t of biparental embryos have already been described.
Marmoset oocytes were either subjected to two series of six electrical puls
es (DC; 2 kV/cm and 70 mu sec) or were incubated in 7% ethanol in PBS. Nine
ty-two percent (68 of 74) and 20% (8 of 40) of marmoset oocytes were activa
ted by electrical stimulus or ethanol, respectively. Parthenogenetic (n = 3
) or in vitro-fertilized (n = 2) embryos were transferred at the 4-cell sta
ge to synchronized recipient female marmosets (n = 5). Progesterone, chorio
nic gonadotropin, and inhibin in the peripheral plasma of recipient animals
were measured. After 33 days of gestation, recipient animals were perfused
and the uteri were collected. The 2 females that had received biparental e
mbryos and 2 of the 3 females that had received parthenogenetic embryos dis
played biochemical and histological evidence of implantation.
This is the first report that a primate embryo comprising only parthenogene
tic cells is capable of implantation. This highlights the need to scrutiniz
e levels of parthenogenesis associated with human assisted reproductive tec
hnologies. Marmoset parthenogenones also provide a unique model for elucida
ting the roles of parental genomes in primate development.