Environmentally relevant exposure to 17α-ethinylestradiol affects the telencephalic proteome of male fathead minnows

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• 作者：Christopher J. Martyniuk ; Kevin J. Kroll ; Nicholas J. Doperalski ; David S. Barber ; Nancy D. Denslow
• 关键词：Pimephales promelas ; iTRAQ ; Quantitative proteomics ; Map-Tau protein
• 刊名：Aquatic Toxicology
• 出版年：2010
• 出版时间：15 July 2010
• 年：2010
• 卷：98
• 期：4
• 页码：344-353
• 全文大小：715 K

文摘

Estrogens are key mediators of neuronal processes in vertebrates. As such, xenoestrogens present in the environment have the potential to alter normal central nervous system (CNS) function. The objectives of the present study were (1) to identify proteins with altered abundance in the male fathead minnow telencephalon as a result of low-level exposure to17α-ethinylestradiol (EE₂), and (2) to better understand the underlying mechanisms of 17β-estradiol (E₂) feedback in this important neuroendocrine tissue. Male fathead minnows exposed to a measured concentration of 5.4 ng EE₂/L for 48 h showed decreased plasma E₂ levels of approximately 2-fold. Of 77 proteins that were quantified statistically, 14 proteins were down-regulated after EE₂ exposure, including four histone proteins, ATP synthase, H+ transporting subunits, and metabolic proteins (lactate dehydrogenase B4, malate dehydrogenase 1b). Twelve proteins were significantly induced by EE₂ including microtubule-associated protein tau (Mapt), astrocytic phosphoprotein, ependymin precursor, and calmodulin. Mapt showed an increase in protein abundance but a decrease in mRNA expression after EE₂ exposure_, suggesting there may be a negative feedback response in the telencephalon to decreased mRNA transcription with increasing Mapt protein abundance. These results demonstrate that a low, environmentally relevant exposure to EE₂ can rapidly alter the abundance of proteins involved in cell differentiation and proliferation, neuron network morphology, and long-term synaptic potentiation. Together, these findings provide a better understanding of the molecular responses underlying E₂ feedback in the brain and demonstrate that quantitative proteomics can be successfully used in ecotoxicology to characterize affected cellular pathways and endocrine physiology.