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This Article Full Text Full Text (PDF) All Versions of this Article: 68/4/1215    most recent biolreprod.102.010488v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Dufour, J. M. Articles by Kim, K. H. Search for Related Content PubMed PubMed Citation Articles by Dufour, J. M. Articles by Kim, K. H. Agricola Articles by Dufour, J. M. Articles by Kim, K. H.

Peroxisome Proliferators Disrupt Retinoic Acid Receptor Alpha Signaling in the Testis¹

^a School of Molecular Biosciences, ^b College of Pharmacy, ^c Center for Reproductive Biology, Washington State University, Pullman, Washington 99164

Peroxisome proliferators include a diverse group of chemicals, some of which have been demonstrated to be testicular toxicants. However, the mechanism by which peroxisome proliferators, such as phthalates, cause testicular damage is not clear. It is known that retinoic acid receptor alpha (RAR) and its retinoic acid ligand, the acid form of vitamin A, are required for spermatogenesis. It has been demonstrated that the absence of RAR gene or vitamin A in the animal leads to testis degeneration and sterility. Therefore, any compound that disrupts the action of vitamin A in the testis could potentially be damaging to male fertility. The current investigation examined a novel hypothesis that a mechanism of degeneration by peroxisome proliferators in the testis is due, in part, to disruption of the critical RAR signaling pathway. We show that peroxisome proliferators were able to disrupt the retinoic acid-induced nuclear localization of RAR and the retinoic acid-stimulated increase in transcriptional activity of a retinoic acid-responsive reporter gene in Sertoli cells. Concomitantly, peroxisome proliferators increased the nuclear localization of PPAR and the transcriptional activity of a peroxisome proliferator-responsive reporter gene in these cells. These results indicate that peroxisome proliferators can indeed shift the balance of nuclear localization for RAR and PPAR, resulting in deactivation of the critical RAR transcriptional activity in Sertoli cells.

¹ This publication was made possible by grant ES09978 from the National Institute of Environmental Health Sciences.

² Correspondence: Kwan Hee Kim, School of Molecular Biosciences, Washington State University, Pullman, WA 99164-4234. FAX: 509 335 1907; khkim{at}wsu.edu

³ These authors contributed equally to this work

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