Interaction of thyroid hormone and steroidogenic acute regulatory (StAR) protein in the regulation of murine Leydig cell steroidogenesis

• Published in: Journal of steroid biochemistry and molecular biology 2001-01, Vol.76 (1), p.167-177
• Main Authors: Manna, Pulak R., Roy, Partha, Clark, Barbara J., Stocco, Douglas M., Huhtaniemi, Ilpo T.
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Biological and medical sciences; DNA Primers; DNA-Binding Proteins - physiology; Fundamental and applied biological sciences. Psychology; Fushi Tarazu Transcription Factors; Homeodomain Proteins; Hormone metabolism and regulation; Leydig cells; Leydig Cells - metabolism; Male; Mammalian male genital system; Mice; Mice, Inbred C57BL; Phosphoproteins - genetics; Phosphoproteins - physiology; Receptors, Cytoplasmic and Nuclear; Receptors, LH - physiology; RNA, Messenger - genetics; Steroidogenesis; Steroidogenic Factor 1; Steroids - biosynthesis; T 3; Transcription Factors - physiology; Triiodothyronine - physiology; Tumor Cells, Cultured; Vertebrates: reproduction
• ISSN: 0960-0760; 1879-1220
• DOI: 10.1016/S0960-0760(00)00156-4

The steroidogenic acute regulatory (StAR) protein, a novel phosphoprotein, is a crucial factor involved in intramitochondrial cholesterol transportation, the rate-limiting step in steroidogenesis. The present investigations were undertaken to elucidate involvement of thyroid hormone and StAR protein in the regulation of steroidogenesis in mouse Leydig cells. Treatment of cells with triiodothyronine (T 3) coordinately augmented the levels of StAR protein, StAR mRNA, and steroid production, and these responses were progressively dependent on expression of steroidogenic factor 1 (SF-1). With regard to steroidogenesis and StAR expression, the T 3 response requires both on-going mRNA and protein synthesis. In addition, the effects of T 3 were acutely modulated at the steroidogenic machinery and luteinizing hormone receptor (LHR) function, while these levels were suppressed following longer periods of exposure to T 3. Furthermore, the inhibition of SF-1 expression by DAX-1 markedly abolished T 3-mediated StAR expression in a time frame, which was consistent with decreased steroid biosynthesis. Specific involvement of SF-1 was further confirmed by assessing the 5′-flanking region of the mouse StAR gene, which identified a region between −254 and −110 bp that was essential for T 3 function. Importantly, it was found that the SF-1 binding site at position −135 bp of the 5′-flanking region was greatly involved in T 3-mediated reporter activity. Electrophoretic mobility shift assays (EMSA) also demonstrated involvement of SF-1 in T 3 function. The relevance of T 3-mediated LHR function was investigated in mice rendered hypo-and hyperthyroid, which accounted for up-regulation in the former and down-regulation in the latter group, respectively. These findings demonstrate a key role of thyroid hormone in maintaining mouse Leydig cell function, where thyroid hormone and StAR protein coordinately regulate steroid hormone biosynthesis.