Liver receptor homolog-1 and steroidogenic factor-1 have similar actions on rat granulosa cell steroidogenesis

Endocrinology. 2007 Feb;148(2):726-34. doi: 10.1210/en.2006-0108. Epub 2006 Nov 9.

Abstract

Granulosa cells express the closely related orphan nuclear receptors steroidogenic factor-1 (SF-1) and liver receptor homolog-1 (LRH-1). To determine whether SF-1 and LRH-1 have differential effects on steroid production, we compared the effects of overexpressing LRH-1 and SF-1 on estrogen and progesterone production by undifferentiated rat granulosa cells. Adenovirus mediated overexpression of LRH-1 or SF-1 had qualitatively similar effects. Neither LRH-1 nor SF-1 alone stimulated estrogen or progesterone production, but when combined with FSH and testosterone, each significantly augmented progesterone production and mRNAs for cholesterol side-chain cleavage enzyme and 3beta-hydroxysteroid dehydrogenase above that observed with FSH alone, with SF-1 being more effective than LRH-1. LRH-1 did not augment FSH-stimulated estrogen production, whereas SF-1 produced only a slight ( approximately 30%) augmentation of FSH-stimulated estrogen production. The stimulatory actions of both were reduced by overexpression of dosage-sensitive sex reversal, adrenal hypoplasia congenita, critical region on the X chromosome, gene 1. Expression of either LRH-1 or SF-1 together with constitutively active protein kinase B in the absence of FSH stimulated progesterone production and mRNAs for 3beta-hydroxysteroid dehydrogenase and cholesterol side-chain cleavage enzyme but did not stimulate estrogen production or mRNA for aromatase. These findings demonstrate that LRH-1 and SF-1 have qualitatively similar actions on FSH-stimulated estrogen and progesterone production, which would suggest that these factors may have overlapping actions in the regulation of steroidogenesis that accompanies granulosa cell differentiation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / genetics
  • Animals
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Cholesterol Side-Chain Cleavage Enzyme / genetics
  • DAX-1 Orphan Nuclear Receptor
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology
  • Drug Interactions
  • Drug Synergism
  • Estrogens / biosynthesis
  • Female
  • Follicle Stimulating Hormone / pharmacology
  • Gene Transfer Techniques
  • Granulosa Cells / drug effects
  • Granulosa Cells / metabolism*
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / physiology*
  • Humans
  • Mice
  • Progesterone / biosynthesis
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins c-akt / physiology
  • RNA, Messenger / metabolism
  • Rats
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / physiology
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology
  • Steroidogenic Factor 1
  • Steroids / biosynthesis*
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / physiology*

Substances

  • DAX-1 Orphan Nuclear Receptor
  • DNA-Binding Proteins
  • Estrogens
  • Homeodomain Proteins
  • NR0B1 protein, human
  • NR5A1 protein, human
  • NR5A2 protein, rat
  • Nr0b1 protein, mouse
  • Nr0b1 protein, rat
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Retinoic Acid
  • Repressor Proteins
  • Steroidogenic Factor 1
  • Steroids
  • Transcription Factors
  • steroidogenic factor 1, mouse
  • steroidogenic factor 1, rat
  • Progesterone
  • Follicle Stimulating Hormone
  • 3-Hydroxysteroid Dehydrogenases
  • Cholesterol Side-Chain Cleavage Enzyme
  • Proto-Oncogene Proteins c-akt