Interleukin-6 decreases estrogen production and messenger ribonucleic acidexpression encoding aromatase during in vitro cytodifferentiation of rat granulosa cell

Citation
K. Tamura et al., Interleukin-6 decreases estrogen production and messenger ribonucleic acidexpression encoding aromatase during in vitro cytodifferentiation of rat granulosa cell, MOL C ENDOC, 170(1-2), 2000, pp. 103-111
Citations number
36
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
MOLECULAR AND CELLULAR ENDOCRINOLOGY
ISSN journal
03037207 → ACNP
Volume
170
Issue
1-2
Year of publication
2000
Pages
103 - 111
Database
ISI
SICI code
0303-7207(200012)170:1-2<103:IDEPAM>2.0.ZU;2-R
Abstract
To elucidate the influence of interleukin-6 (IL-6) on the maturation of rat granulosa cell (GC), we have established a differentiation model of rat GC in vitro and examined the expression of IL-6 and its receptors, and its po ssible actions during GC maturation. Bioactive IL-6 was detectable in the c onditioned media of GC at similar to 2.5 ng/ml/24 h per 5 x 10(5) cells. Re verse transcription-polymerase chain reaction (RT-PCR) analysis revealed th at messenger RNAs encoding components of functional IL-6 receptor, namely b oth ligand-binding subunit (IL-6R) and gp130, were expressed in GC. Treatme nt of GC with IL-6 for 72 h during the process of in vitro GC maturation do se-dependently inhibited the accumulation of estradiol-17 beta (E-2) and th e expression of cytochrome P450 aromatase (P450arom). IL-6 did not change n itric oxide (NO) production and inducible NO synthase expression, implying that IL-6-induced suppression on E-2 levels is dissociated with NO expressi on. Further, GC which had been incubated with neutralizing anti-IL-6 antibo dy showed a distinct increase in the levels of P450arom mRNA. These results suggest that IL-6 may attenuate E-2 production partially by inhibiting the expression of aromatase mRNA as an intraovarian regulator for suppressing GC maturation. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.