In vitro exposure to environmental tobacco smoke induces CYP1B1 expression in human luteinized granulosa cells

Reprod Toxicol. 2006 Nov;22(4):731-7. doi: 10.1016/j.reprotox.2006.06.001. Epub 2006 Jun 18.

Abstract

Women smokers and women exposed to environmental tobacco smoke (ETS) have reduced ovarian function as evidenced by an earlier menopause, reduced follicular numbers, decreased levels of circulating estradiol, and decreased conception rates; however, the mechanism of action of altered ovarian function by ETS is poorly understood. The direct effects of ETS were evaluated using human luteinized granulosa cells (HLGCs) exposed to ETS in primary cell culture. Exposure to ETS caused a decrease in both estradiol and progesterone production. There was a concentration dependent increase in CYP1B1 gene and protein expression without a change in catechol-O-methyltransferase (COMT) expression. This is the first report of CYP1B1 induction secondary to ETS exposure in cells from the human ovary. CYP1B1 metabolizes both endogenous estrogens and polyaromatic hydrocarbons in ETS to a variety of reactive species and may contribute to the complex effects of ETS on ovarian function.

Publication types

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

MeSH terms

  • Aryl Hydrocarbon Hydroxylases / genetics*
  • Aryl Hydrocarbon Hydroxylases / metabolism
  • Blotting, Western / methods
  • Catechol O-Methyltransferase / metabolism
  • Cells, Cultured
  • Cytochrome P-450 CYP1B1
  • Dose-Response Relationship, Drug
  • Estradiol / metabolism
  • Estrogen Antagonists / pharmacology
  • Female
  • Gene Expression / drug effects
  • Granulosa Cells / cytology
  • Granulosa Cells / drug effects
  • Granulosa Cells / metabolism*
  • Humans
  • Luteinization / metabolism
  • Polychlorinated Dibenzodioxins / pharmacology
  • Progesterone / antagonists & inhibitors
  • Progesterone / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Tobacco Smoke Pollution / analysis*

Substances

  • Estrogen Antagonists
  • Polychlorinated Dibenzodioxins
  • Tobacco Smoke Pollution
  • Progesterone
  • Estradiol
  • Aryl Hydrocarbon Hydroxylases
  • CYP1B1 protein, human
  • Cytochrome P-450 CYP1B1
  • Catechol O-Methyltransferase