Journal
EXPERIMENTAL BIOLOGY AND MEDICINE
Volume 234, Issue 5, Pages 513-521Publisher
SAGE PUBLICATIONS LTD
DOI: 10.3181/0812-RM-369
Keywords
ApoER2; glutathione peroxidase; qRT-PCR; mRNA; selenoprotein P; selenoprotein W; selenoproteome
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Funding
- National Institutes of Health [DK74184, T32-DK07665]
- University or Wisconsin Agricultural Experiment Station [WIS04909]
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK074184, T32DK007665] Funding Source: NIH RePORTER
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Selenium (Se) plays a critical role in testis, sperm, and reproduction, and testis Se levels are remarkably maintained in Se deficiency. In most other tissues, Se levels decrease dramatically as do levels of most selenoproteins and levels of a subset of Se-regulated selenoprotein mRNAs. Because of the recent identification of key molecules in the targeted trafficking of Se to the testis, we examined the hierarchy of Se regulation in testis by determining the dietary Se regulation of the full testis selenoproteome in rats fed graded levels of Se (0 to 0.8 mu g Se/g) as Na2SeO3 for 28 d. Se status did not significantly affect testis weight or glutathione peroxidase 4 (Gpx4) activity (P > 0.05). qRT-PCR analysis of selenoprotein mRNA expression revealed that 21 of the 24 selenoprotein mRNAs and ApoER2 mRNA (the selenoprotein P [Sepp1] receptor) were also not regulated significantly by dietary Se status. In contrast, Gpx1 activity decreased to 28% of Se-adequate levels, and mRNA levels for Gpx1, Sepp1, and Sepw1 (selenoprotein W) decreased significantly in Se-deficient rats to 45, 46, and 55%, respectively, of Se-adequate plateau levels. Overlap of hyperbolic Gpx4 activity and Sepw1 mRNA response curves with testis Se concentration, all with minimum dietary Se requirements < 0.016 mu g Se/g, showed the priority for synthesis of Gpx4. Higher minimum dietary Se requirements of 0.04 mu g Se/g for Gpx1 activity and Sepp1 mRNA, and the even higher minimum dietary Se requirement of 0.08 mu g Se/g for Gpx1 mRNA, suggest that the hierarchy of these biomarkers reflects distinct, lower priority pools, cell types, and roles for Se within the testis. Exp Biol Med 234:513-521, 2009
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