Hormonal regulation and characterisation of the aldehyde oxidase-like gene of hamster Harderian gland

J Steroid Biochem Mol Biol. 2008 Nov;112(1-3):157-63. doi: 10.1016/j.jsbmb.2008.09.009. Epub 2008 Sep 20.

Abstract

The HG is a compound tubulo-alveolar gland located in the orbital cavity of the majority of vertebrates. In the golden hamster it shows a clear cut sexual dimorphism in both morphological and biochemical parameters such as cell types, protein pattern, lipid metabolism, porphyrin content, steroid hormone receptor expression. In a previous study we found that in primary culture of male hamster Harderian gland (HG), androgens (A) increase the MHG07 (male Harderian gland) expression and this effect is abrogated by both flutamide and cycloheximide. The present study represents a deeper analysis on MHG07 regulation by other members of steroid/thyroid hormone superfamily. Estrogens (E) impair the stimulatory effect of A and after the addition of a pure anti-estrogen, ICI 164,384, the negative effect of E is abrogated. Dexamethasone (Dex), used alone or in combination with A negatively affect the MHG07 expression. Also T(3) increases the expression of MHG07 mRNA. Progesterone (P) does not affect the expression of MHG07 mRNA. The use of cycloheximide abrogates the effect of steroids, suggesting that the latter act through their own receptors. Dose-response experiments show that low steroid concentrations (10(-12)M) are sufficient to affect the MHG07 expression. It is argued that the expression of MHG07 is under a highly coordinate relationship between androgen, estrogen, glucocorticoid, retinoic acid and thyroid hormones.

MeSH terms

  • Aldehyde Oxidase / metabolism*
  • Animals
  • Cricetinae
  • Gene Expression Regulation
  • Gonadal Steroid Hormones / pharmacology
  • Gonadal Steroid Hormones / physiology*
  • Harderian Gland / drug effects
  • Harderian Gland / metabolism*
  • Male
  • Mesocricetus
  • Receptors, Androgen / metabolism

Substances

  • Gonadal Steroid Hormones
  • Receptors, Androgen
  • Aldehyde Oxidase