Cytotoxic and apoptotic effects of 17α-ethynylestradiol and diethylstilbestrol on CHO-K1 cells

There is considerable concern about the substances present in the environment and their potential to interfere with the endocrine system of vertebrates. Among these, the so-called endocrine-disrupting compounds, which can modulate or disrupt developmental and reproductive processes, substances with...

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Published in:Food technology and biotechnology 2011-10, Vol.49 (4), p.447-447
Main Authors: Radosevic, Kristina, Novak, Ruder, Slivac, Igor, Mihajlovic, Mirna, Dumic, Jerka, Kniewald, Zlatko, Srcek, Visnja Gaurina
Format: Article
Language:English
Subjects:
17α-ethynylestradiol
Apoptosis
Cell lines
CHO-K1 cells
cytotoxicity
Diethylstilbestrol
Endocrine disruptors
necrosis
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Summary:There is considerable concern about the substances present in the environment and their potential to interfere with the endocrine system of vertebrates. Among these, the so-called endocrine-disrupting compounds, which can modulate or disrupt developmental and reproductive processes, substances with estrogenic activity have attracted most attention. Concerns about the presence of these compounds in the environment have led to the development of screening and testing assays that are able to detect such substances and evaluate their potential to induce adverse effects. In vitro systems such as mammalian and fish cell lines have become of growing importance in toxicity testing of such compounds. The cytotoxic and apoptotic effects induced by 17α-ethynylestradiol and diethylstilbestrol were studied on CHO-K1 cell line. Trypan blue exclusion method was used to determine the cell viability. Cytotoxicity of 17α-ethynylestradiol (0.34-34 µM) and diethylstilbestrol (0.37-37 µM) was found to be concentration-dependent with [IC.sub.50] values of 12.8 and 10.4 µM after 72 h of exposure, respectively. In treated CHO-K1 culture cell death was assessed by determining morphological changes by haematoxilyn and eosin staining, nuclear morphology by fluorescein diacetate/propidium iodide staining and fluorescence microscopy, DNA fragmentation by TUNEL method and translocation of phosphatidyl serine by flow cytometry. The obtained results showed that 17α-ethynylestradiol induced apoptosis, while diethylstilbestrol induced necrosis in the treated CHO-K1 cells. Key words: apoptosis, CHO-K1 cells, cytotoxicity, diethylstilbestrol, 17α-ethynylestradiol, necrosis
ISSN:1330-9862
1334-2606