Journal of Andrology
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Published-Ahead-of-Print October 2, 2008, DOI:10.2164/jandrol.108.006387
Journal of Andrology, Vol. 30, No. 2, March/April 2009
Copyright © American Society of Andrology
DOI: 10.2164/jandrol.108.006387

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cAMP-Induced Expression of the Orphan Nuclear Receptor Nur77 in MA-10 Leydig Cells Involves a CaMKI Pathway

LUC J. MARTIN*,{ddagger}, NICOLAS BOUCHER*,{ddagger}, BASSAM EL-ASMAR* AND JACQUES J. TREMBLAY*,{dagger}

From the * Department of Reproduction, Perinatal, and Child Health, Le Centre Hospitalier Universitaire de Québec (CHUQ) Research Centre, and the {dagger} Centre for Research in Biology of Reproduction, Department of Obstetrics and Gynecology, Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada.

Correspondence to: Dr Jacques J. Tremblay, Reproduction, Perinatal, and Child Health, CHUQ Research Centre, CHUL Room T1-49, 2705 Laurier Blvd, Quebec City, QC Canada G1V 4G2 (e-mail: Jacques-J.Tremblay{at}crchul.ulaval.ca).


The Nur77 (Nr4a1) gene, encoding the orphan nuclear receptor NUR77 (NR4A1), is an immediate early response gene whose expression is rapidly induced by a variety of physiologic stimuli. Nur77 is expressed in several organs, including the classic steroidogenic tissues: gonads and adrenal. In MA-10 Leydig cells, NUR77 has been shown to regulate expression of several genes involved in steroidogenesis and male sex differentiation. In Leydig cells, androgen biosynthesis is controlled primarily by the pituitary gonadotropin luteinizing hormone (LH) acting via its receptor (LH-R), which in turn activates the adenylate cyclase/cyclic adenosine monophosphate (cAMP) signaling pathway. Even though Nur77 expression is induced both at the mRNA and protein levels in response to LH/forskolin/cAMP in Leydig cells, the mechanisms involved remain largely unknown. Here, we report that cAMP-mediated induction of Nur77 expression at the protein, mRNA, and promoter levels in MA-10 cells involves different mechanisms. We found that increased NUR77 protein requires transcription and translation, whereas increased Nur77 mRNA does not require de novo protein synthesis, and would therefore rely on transcription factors already present in the cell. In addition, our detailed analysis of the Nur77 promoter in MA-10 cells revealed that distinct regulatory elements are involved in basal and cAMP-induced Nur77 transcription. Finally, we found that maximal cAMP-mediated increase in Nur77 promoter activity involves a Ca2+/calmodulin kinase (CaMK)-dependent pathway and that Ca2+/calmodulin kinase I regulates Nur77 promoter activity in Leydig cells. Thus, our findings demonstrate the involvement of various mechanisms in the regulation of Nur77 expression in MA-10 Leydig cells, including a previously uncharacterized CaMK pathway.

     Key words: NR4A1, NGFI-B, forskolin, luteinizing hormone, steroidogenesis, Ca2+/calmodulin kinase I






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