Matrix metalloproteinase-9 (MMP-9) is proposed to play an important role within the uterus from the time of post-natal uterine development through the period of establishment of pregnancy and subsequent parturition. Further, over-expression of MMP-9 or an imbalance in the MMP-9 to tissue inhibitor (TIMP) ratio has been associated with uterine pathologies such as dysfunctional uterine bleeding, endometriosis, infertility and endometrial carcinoma. Despite the proposed importance of this MMP in normal uterine physiology and uterine diseases, the steroidal regulation of MMP-9 is not clearly understood. Preliminary data in the current application suggest yet another layer of complexity in the regulation of this MMP. We present compelling evidence that MMP-9 transcript expression is decreased in response to early estrogen treatment, but protein and MMP-9 activity significantly increase. These observations suggest a novel and complex mechanism for estrogenic induction of uterine MMP-9 which, to the best of our knowledge, does exist in other organ or cell systems. As such, the objective of this proposal is to explore the mechanisms which impart this unique regulatory system within the uterus. We hypothesize that estrogen regulates uterine MMP-9 translation via a mechanism which includes microRNAs (miRNAs). To test this hypothesis, we propose two Specific Aims which will 1) characterize uterine miRNA expression in response to estrogen treatment, and 2) functionally demonstrate that those identified miRNA regulate MMP-9 translation within the uterus. In doing so, new light will be shed upon the estrogenic regulation of this important uterine MMP as well as the potential role of the uterine miRNA system in response to estrogen treatment. Collectively, the findings from the proposed studies will expand our knowledge on regulatory mechanisms for MMP-9 expression and provide the pioneering documentation of the uterine miRNA profile. These results will lead to further exploration of this system within the uterus and provide a better understanding on how uterine MMPs may be regulated and what functions miRNAs may play in this vital female organ. Summary: Controlled expression of matrix metalloproteinase-9 (MMP-9) is vital for normal uterine physiology while abnormal expression of MMP-9 is associated with uterine disease. Despite the importance of MMP-9 within the uterus, its regulation is poorly understood. The proposed studies will examine the complex regulation of MMP-9 within the uterus and decipher the novel role of microRNAs in the regulation of this protease. Enhancing our understanding on the regulation of MMP-9 expression may lead to the establishment of novel approaches to counteract mis-expression of this protease and the diseases associated with it. ? ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21HD056387-02
Application #
7471407
Study Section
Integrative and Clinical Endocrinology and Reproduction Study Section (ICER)
Program Officer
Yoshinaga, Koji
Project Start
2007-07-18
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2010-06-30
Support Year
2
Fiscal Year
2008
Total Cost
$180,075
Indirect Cost
Name
University of Kansas
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Nothnick, Warren B (2016) Non-coding RNAs in Uterine Development, Function and Disease. Adv Exp Med Biol 886:171-189
Nothnick, Warren B; Healy, Caitlin; Hong, Xiaoman (2010) Steroidal regulation of uterine miRNAs is associated with modulation of the miRNA biogenesis components Exportin-5 and Dicer1. Endocrine 37:265-73
Nothnick, Warren B; Healy, Caitlin (2010) Estrogen induces distinct patterns of microRNA expression within the mouse uterus. Reprod Sci 17:987-94
Nothnick, Warren B (2008) Regulation of uterine matrix metalloproteinase-9 and the role of microRNAs. Semin Reprod Med 26:494-9