4.7 Article

Bcl-2 and Caspase 3 mRNA levels in the testes of gudgeon, Gobio gobio, exposed to ethinylestradiol (EE2)

Journal

AQUATIC TOXICOLOGY
Volume 98, Issue 3, Pages 304-310

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aquatox.2010.02.016

Keywords

Bcl-2; Caspase 3; Ethinylestradiol; Early spermatogenesis

Funding

  1. 'Fonds pour la formation a la Recherche dans l'Industrie et dans l'Agriculture' (FRIA, Belgium)

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Apoptosis inhibition has been reported in the male reproductive tract of teleost fish exposed to 17 beta-estrogen or estrogen-like compounds. In order to understand the molecular mechanisms of cell death inhibition, this study examined 2 genes involved in the apoptotic pathway, Bcl-2 and Caspase 3, an antiapoptotic and a pro-apoptotic genes, respectively. Partial cDNA sequences of Bcl-2 and Caspase 3 were cloned from gudgeon (Gobio gobio), a common European cyprinid fish. To follow mRNA levels of Bcl-2 and Caspase 3 under xenoestrogen exposure, we first performed an in vitro experiment on fish testis exposed to the most potent xenoestrogen found in the environment, ethinylestradiol (EE2). We further studied mRNA expression of both genes in the testis of fish exposed to xenoestrogens in situ. In the in vitro experiment, fragments of gudgeon testis were exposed for 21 days to 10(-3), 10(-2), 10(-1), 1 and 10 mu g/L of EE2, as well as to positive (10(-1) mu g/L of E2) and ethanol control medium. Results showed a significant induction of Bcl-2 mRNA at 10(-1) mu g/L (p<0.05). Surprisingly, Caspase 3, a cell death effector, displayed the same profile as observed for the anti-apoptotic gene Bcl-2. In the experiment on wild gudgeon exposed from birth to an estrogenic sewage treatment plant effluent, the mRNA expression of Bcl-2 and Caspase 3 in feminized fish (ovotestis) was not significantly different due to high variability of expression between individuals. At the current state of knowledge on spermatogenesis disruption in teleost fish, in vitro studies seem better adapted than in situ investigations to enlighten the molecular pathway of apoptosis inhibition in testis exposed to xenoestrogens. (C) 2010 Elsevier B.V. All rights reserved.

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