Molecular Human Reproduction, Vol. 7, No. 7, 681-689,
July 2001
© 2001 European Society of Human Reproduction and Embryology
Implantation and pregnancy |
Apoptosis in the normal human amnion at term, independent of Bcl-2 regulation and onset of labour
1 Department of Obstetrics and Gynecology and 2 Department of Anatomy and Biology, Osaka Medical College, 2–7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan
Abstract
This study was designed to detect apoptosis in the human amnion and to elucidate the signalling pathway involved in its regulation. Samples of human amnion were obtained from 34 women (weeks 11–42 of gestation) and studied using the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labelling (TUNEL) method with light microscopy (LM) and transmission electron microscopy (TEM). Apoptotic regulators in the samples were studied by immunohistochemistry and caspase activity assay. The TUNEL method with LM demonstrated that the percentage of TUNEL-positive cells in the amniotic epithelium was the highest in weeks 40–41 of gestation (P < 0.05) independent of the onset of labour, and the cells were often detached from the epithelium into the amniotic cavity at term. The TUNEL method with TEM clearly showed the characteristic features of apoptosis such as the nuclear condensed chromatin with abundant free 3'-OH DNA ends, cell shrinkage and a decrease in the number of desmosomes, except for the presence of apoptotic bodies. Fas and Fas ligand (FasL) were constantly expressed on apical membranes of amniotic epithelial cells from weeks 16–27 through to 40–41 of gestation, while no Bcl-2 expression was observed throughout the gestational periods. Activities of caspase-3 and caspase-8, but not of caspase-9, were higher in weeks 40–41 than those from weeks 16–27 of gestation (P < 0.01). We conclude that apoptosis in term amniotic epithelium is independent of Bcl-2 regulation and onset of labour, and may play an important role in the fragility and rupture of human fetal membranes at term.
amnion/apoptosis/caspase/Fas antigen/Fas ligand
Notes
3 To whom correspondence should be addressed. E-mail: an1001{at}art.osaka-med.ac.jp
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