
pmid: 14748698
Abstract During mammalian embryonic development, abnormal eggs and embryos are eliminated by apoptosis; however, the precise apoptotic pathways remain as yet unidentified. In the present study, expression of Fas and Fas ligand - the proximal members of the death receptor pathway, was evaluated in mouse preimplantation embryos by immunofluorescence and in situ hybridization techniques. Ovulated oocytes were collected from oviducts of cyclic mice on the day of oestrus (day 0), and one-cell, two-cell embryos and eight-cell morulae were collected from oviducts of mated animals on days 1, 2 and 3 of pregnancy, respectively. Blastocysts were flushed from the uterine horns on day 4. Expression of Fas and Fas L mRNAs and proteins was absent from embryos at days 0, 1 and 2. A marked increase in Fas and Fas L mRNA and protein expression was detected in all morphologically normal embryos on day 3 and day 4. In addition, embryos on days 3 and 4 were positive for terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL) staining; however, absence of caspase 8 and 3 and intense localization of proliferating cell nuclear antigen confirmed the proliferative status of these embryos. Furthermore, TUNEL staining was absent in postimplantation embryonic sections obtained on day 6. The results of the present studies thus indicate an equilibrium between proliferation and apoptosis in the preimplantation embryo.
Fas Ligand Protein, Membrane Glycoproteins, Apoptosis, Mice, Inbred Strains, Immunohistochemistry, Embryonic and Fetal Development, Mice, Blastocyst, In Situ Nick-End Labeling, Oocytes, Animals, Female, RNA, Messenger, fas Receptor, Biomarkers, In Situ Hybridization
Fas Ligand Protein, Membrane Glycoproteins, Apoptosis, Mice, Inbred Strains, Immunohistochemistry, Embryonic and Fetal Development, Mice, Blastocyst, In Situ Nick-End Labeling, Oocytes, Animals, Female, RNA, Messenger, fas Receptor, Biomarkers, In Situ Hybridization
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