Regulation of MMP-9 expression and activity in the mouse uterus by estrogen

被引:26
|
作者
Zhang, Xuan
Christenson, Lane K.
Nothnick, Warren B.
机构
[1] Univ Kansas, Ctr Med, Dept Obstet & Gynecol, Kansas City, KS 66160 USA
[2] Univ Kansas, Sch Med, Dept Mol & Integrat Physiol, Kansas City, KS USA
关键词
uterus; 17-beta-estradiol; progesterone; MMP-9;
D O I
10.1002/mrd.20582
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinases (MMPs) are spatiotemporally expressed in the uterus across normal estrous and menstrual cycles and are known to participate in the extensive endometrial tissue remodeling. MMP-9/gelatinase B is one of the major MMPs found in the uterus that modulates uterine biology during various reproductive processes. Although it seems that uterine MMP-9 is under ovarian steroid hormonal control, there are conflicting reports regarding steroidal hormonal regulation of MMP-9 expression, and there is little information on the effects of estrogen in vivo in this respect. We therefore examined the steroidal regulation of MMP-9 within the mouse uterus. Female mice (2-3 months old) were ovariectomized and treated with estradiol-17 beta (E-2) or E-2 + progesterone (P-4) and uterine gelatinase activity and expression were determined. Gelatin zymography revealed that E-2 alone or in combination with P-4 increased MMP-9 activation, whereas Northern analysis showed that E-2 decreased MMP-9 steady state mRNA expression and an estrogen receptor antagonist ICI-182, 780 blocked this effect. In contrast, uterine MMP-2 expression and activity were not affected by steroidal treatments. Pretreatment with a transcription inhibitor actinomycin D or translation inhibitor cycloheximide indicates that E-2 regulates uterine MMP-9 at multiple points, involving transcriptional and posttranscriptional control as well as modulation of inhibitor activities. Collectively, these data suggest that E-2 regulates uterine MMP-9 expression and activity in vivo via a complex mechanism. This estrogen regulation of MMP-9 activity may play an important role in uterine tissue remodeling.
引用
收藏
页码:321 / 331
页数:11
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