SF-1 (NR5A1) expression is stimulated by the PKA pathway and is essential for the PKA-induced activation of LIPE expression in Y-1 cells

Mol Cell Biochem. 2015 Oct;408(1-2):139-45. doi: 10.1007/s11010-015-2489-9. Epub 2015 Jun 30.

Abstract

In the adrenal cortex, corticotropin induces the expression of several genes encoding proteins involved in the synthesis and intracellular transport of steroid hormones via the protein kinase A (PKA) signalling pathway, and this process is mediated by steroidogenic factor-1 (SF-1). This study was designed to elucidate the influence of the PKA and PKC pathways on the expression of the SF-1 gene in mouse adrenocortical cells, line Y-1. It has also been attempted to answer the question whether or not SF-1 plays a role in the PKA-induced expression of LIPE gene encoding hormone-sensitive lipase/cholesteryl esterase, which supplies cholesterol for steroid hormone synthesis. In this study, we found that stimulation of the PKA pathway caused a significant increase in SF-1 expression, and that this effect was abolished by the PKA inhibitor, H89. Decreased SF-1 gene transcript levels were seen with the simultaneous activation of PKA and PKC, suggesting a possible interaction between the PKA and PKC pathways. It was also observed that SF-1 increased the transcriptional activity of the LIPE gene by interacting with the SF-1 response element located in promoter A. Moreover, transient silencing of SF-1 expression with specific siRNAs abolished PKA-stimulated transcription of the LIPE gene, indicating that SF-1 is an important regulator of LIPE expression in Y-1 cells and thus could play a role in the regulation of the cholesterol supply for adrenal steroidogenesis.

Keywords: HSL; LIPE; PKA; SF-1; Y-1 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex / cytology
  • Adrenal Cortex / metabolism*
  • Animals
  • Cell Line
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Isoquinolines / pharmacology
  • Mice
  • Promoter Regions, Genetic
  • Protein Kinase C / metabolism*
  • Signal Transduction / drug effects
  • Steroidogenic Factor 1 / genetics*
  • Steroidogenic Factor 1 / metabolism
  • Sterol Esterase / genetics*
  • Sulfonamides / pharmacology

Substances

  • Isoquinolines
  • Steroidogenic Factor 1
  • Sulfonamides
  • steroidogenic factor 1, mouse
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Sterol Esterase
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide