Estrogen receptor-beta regulates tryptophan hydroxylase-1 expression in the murine midbrain raphe

Biol Psychiatry. 2005 Apr 15;57(8):938-42. doi: 10.1016/j.biopsych.2005.01.014.

Abstract

Background: Distinct expression patterns of estrogen receptor (ER)-alpha and ER-beta are displayed in the murine central nervous system. ER-beta is the predominant form of the receptor expressed in the murine midbrain dorsal raphe nucleus (DRN). Tryptophan hydroxylase (TPH) is abundantly expressed in the serotonergic neurons of the DRN and is regulated by estrogen in both the monkey and the guinea pig.

Methods: In this study we used immunocytochemistry to show that ER-beta and TPH are colocalized in the serotonergic cells of the murine DRN. We utilized the ER-alpha and ER-beta gene deletion mouse models and in situ hybridization to demonstrate that ER-beta is responsible for regulating TPH1 mRNA expression.

Results: Estrogen increased TPH1 mRNA expression in the DRN of wild type and ER-alpha knockout mice (alpha-ERKO) but not ER-beta knockouts (beta-ERKO).

Conclusions: These data indicate that ER-beta is responsible for mediating estrogen regulated TPH1 expression in the murine DRN.

MeSH terms

  • Animals
  • Cells, Cultured
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / physiology
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / physiology*
  • Immunohistochemistry
  • In Situ Hybridization
  • Mesencephalon / enzymology
  • Mesencephalon / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism
  • Ovariectomy
  • Raphe Nuclei / enzymology
  • Raphe Nuclei / metabolism*
  • Serotonin / physiology
  • Tryptophan Hydroxylase / biosynthesis*

Substances

  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Serotonin
  • Tph1 protein, mouse
  • Tryptophan Hydroxylase