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Endocrinology Vol. 144, No. 3 767-776
Copyright © 2003 by The Endocrine Society


ARTICLE

Expression of Aryl Hydrocarbon Receptor and Aryl Hydrocarbon Receptor Nuclear Translocator Messenger Ribonucleic Acids and Proteins in Rat and Human Testis

Rüdiger Schultz, Janne Suominen, Tanja Värre, Harri Hakovirta, Martti Parvinen, Jorma Toppari and Markku Pelto-Huikko

Department of Developmental Biology, Tampere University (R.S., T.V., M.P.-H.), FIN-33014 Tampere, Finland; Departments of Dermatology (R.S.) and Pathology (M.P.-H.), Tampere University Hospital, FIN-33520 Tampere, Finland; Department of Pediatrics and Physiology, Turku University Hospital (J.S., H.H., J.T.), and Department of Anatomy, University of Turku (M.P.), FIN-20520 Turku, Finland

Address all correspondence and requests for reprints to: Markku Pelto-Huikko, M.D., Ph.D., Department of Developmental Biology, Tampere University Medical School, FIN-33014 Tampere, Finland. E-mail: blmapel{at}uta.fi.

Dioxins, e.g. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), use the aryl hydrocarbon receptor (AHR)/aryl hydrocarbon receptor nuclear translocator (ARNT) receptor complex to mediate their toxic actions. In addition to interaction with environmental pollutants, several transcription factors, steroid receptors, and growth factors are capable interacting with the AHR/ARNT complex, which suggests a constitutive role for the receptor complex.

The testis has been reported to be among the most sensitive organs to TCDD exposure. Our experiments revealed a complex distribution of AHR and ARNT mRNAs and proteins in rat and human testis. AHR and ARNT immunoreactivities could be detected in the nuclei of interstitial and tubular cells. The incubation of seminiferous tubules in a serum-free culture medium resulted in up-regulation of AHR mRNA, which could be depressed by adding FSH to the culture medium. Furthermore, the incubation of tubular segments with a solution of 1 or 100 nM TCDD resulted in a 2- to 3-fold increase in apoptotic cells. Thus, up-regulation of AHR in cultured tubular segments and consecutive depression by FSH suggest a role for AHR in controlled cell death during spermatogenesis. We suggest that AHR and ARNT mediate effects by direct action on testicular cells in the rat and human testis.




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