Apoptotic cell death of oestrogen activated lactotrophs induced by tamoxifen
Maria del Pilar Aoki1, Elsa Orgnero, Agustín Aoki
1Department of Clinical Chemistry, Immunology, Faculty of Chemical Sciences, National University of Córdoba, Ala 1 subsuelo. 5000 Córdoba, Argentina. paoki@bioclin.fcq.unc.edu.ar
Abstract:
Stimulation and inhibition of lactotroph cells cause remarkable morphological and functional changes. In keeping with these changes, the size of the lactotroph cell population undergoes striking alterations due to proliferation or cell death. Factors involved in the induction of apoptosis of pituitary cells are not well established. We demonstrated earlier that oestrogens prevent lactotroph cells of female rats to die by apoptosis induced by bromocryptine treatment, a fact that can be reversed in ovariectomised rats. In this study, we developed experimental models for in vivo and in vitro studies to gain further insight on the survival effect of oestrogens on lactotrophs. In rats pretreated with oestrogens, tamoxifen generates a massive cell death by apoptosis as validated by the TUNEL technique and DNA electrophoresis of pituitary gland. On electron microscope observations, numerous lactotrophs exhibited progressive morphological changes in the nuclei compatible with the apoptotic process. The cells remaining intact also exhibit signs of inhibition due to a significant transformation of regular lactotrophs in atypical subtypes. In pituitary cell cultures exposed to tamoxifen and oestrogen simultaneously, most of the lactotrophs displayed features of apoptosis in the nucleus. The present reports gathered new evidences on the apoptogenic potential of tamoxifen on lactotroph cells, and corroborates the contribution of oestrogens to sustain both a balanced population of lactotrophs and a competent secretory activity. The concept that opposed activities, such as inhibition and stimulation, can activate apoptosis is also strengthen by these observations.
Insights
Oestrogens protect lactotroph cells from apoptosis induced by tamoxifen. This study reveals tamoxifen
Area of Science:
- Endocrinology
- Cell Biology
- Pituitary Gland Research
Background:
- Lactotroph cell population size is regulated by proliferation and cell death.
- Factors inducing apoptosis in pituitary cells are not fully understood.
- Oestrogens are known to prevent apoptosis in lactotroph cells.
Purpose of the Study:
- To investigate the survival effects of oestrogens on lactotrophs.
- To explore the mechanisms of oestrogen-mediated protection against apoptosis.
- To understand the role of tamoxifen in lactotroph cell death.
Main Methods:
- Development of in vivo and in vitro experimental models.
- Treatment of rats with oestrogens and tamoxifen.
- Analysis of pituitary glands using TUNEL technique and DNA electrophoresis.
- Electron microscopy to observe cellular morphology.
- In vitro culture of pituitary cells exposed to tamoxifen and oestrogen.
Main Results:
- Tamoxifen induced massive apoptosis in lactotroph cells of oestrogen-pretreated rats.
- Morphological changes consistent with apoptosis were observed in lactotroph nuclei.
- Intact lactotrophs showed signs of inhibition and transformation into atypical subtypes.
- Simultaneous exposure to tamoxifen and oestrogen in cell cultures resulted in nuclear apoptosis.
Conclusions:
- Tamoxifen exhibits apoptogenic potential on lactotroph cells.
- Oestrogens contribute to maintaining a balanced lactotroph population and secretory function.
- Opposing cellular activities, like inhibition and stimulation, can trigger apoptosis.
Related Concept Videos
Overview of Cell Death
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...
Apoptosis
The Extrinsic Apoptotic Pathway
The Intrinsic Apoptotic Pathway
Phagocytosis of Apoptotic Cells
Normal cells contain receptors that prevent them from being recognized by phagocytes.
Cellular Injury V: Apoptosis and Autophagy


