Temporal Changes of c-fos, c-jun, and Heat Shock Protein 25 mRNA in Rat Uterus following Estradiol Treatment.
- Author:
Youngki LEE
;
Sung Rye KIM
- Publication Type:Original Article
- MeSH:
Adult;
Animals;
Axis, Cervical Vertebra;
Blotting, Northern;
Estradiol*;
Estrogen Receptor Modulators;
Estrogens;
Female;
Gene Expression;
Heat-Shock Proteins*;
Hot Temperature*;
Humans;
Rats*;
RNA, Messenger*;
Tamoxifen;
Transcription Factors;
Uterus*
- From:Korean Journal of Fertility and Sterility
1999;26(2):149-156
- CountryRepublic of Korea
- Language:English
-
Abstract:
SUMMARY: Steroid hormone is known to cause the dynamic changes of mammalian uterus during reproductive cycle, which are modulated via hypothalamus-pituitary -gonad reproductive endocrine axis. Although there were so many studies about estrogenic regulation of uterine growth and differentiation. There is little information about the effect of estrogen on the expression of various transcription factors involved in gene expression. Thus the present study was designed to demonstrate E induced expression of c-fos, c-jun, hsp25 mRNA in rat uterus. Employing Northern blot analysis, we studied the temporal expressions of c-fos, c-jun, and hsp25 messenger RNAs (mNAs) elicited by a single 17beta-estradiol(E) treatment in the uteri of bilaterally ovariectomized adult rats. c-fos, c-jun, and hsp25 mRNA levels were increased and peaked at 3 h after E administration, and then c-fos and c-jun mRNA levels were rapidly decreased to basal control level while, increased hsp25 mRNA levels were sustained till 12 h post E treatment. To test the estrogenic effect on the increase of c-fos, c-jun, and hsp25 mRNA levels, we also examined the effects of antiestrogen (tamoxifen). Pretreatment with tamoxifen effectively blocked the E-induced increase of c-fos, c-jun, and hsp25 mRNA levels at 3 h post E treatment. Present results suggest that transient increase of c-fos and c-jun protooncogene mRNA at the early time and simultaneous expression of hsp25 mRNA contribute to the response of uterine tissues to E in adult female rats.
