K.SRIDHAR RAO1, S ZANOTTI2, A.G REDDY1, F RAUCH2, H.G MANNHERZ2, P.D GUPTA1
1Centre for Cellular & Molecular Biology, Hyderabad 500 007, India
2RUHR-Universitat Bochum, Medizinische Fakultat, Institut fur Anatomie, Abteilung fur Anatomie und Embryologie, D-44780, Bochum, Germany
Tóm tắt
Rat vaginal epithelial cells (VEC) undergo division and differentiation under the influence of oestradiol in a programmed manner. The differentiation process of VEC leads to keratinization, cornification and subsequent desquamation of the dead cells. This process of programmed cell death, referred to as terminal differentiation may share some common pathways with cell death by apoptosis but differ substantially in many aspects. Terminal differentiation of VEC is accompanied by the loss of majority of the organelles including the nucleus. To understand the mechanisms that underlie this process we have analysed the regulation of DNase I (a key effector of apoptotic cell death) in rat VEC under the influence of oestradiol. The present study demonstrates that under physiological conditions, cell death in the VEC is mainly through terminal differentiation although a few cells may undergo apoptotic death involving DNA fragmentation. Unaltered levels of bcl‐2 message upon oestradiol administration suggest an important role played by this molecule in preventing death of the VEC by apoptosis.
