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BOR - Papers in Press, published online ahead of print June 8, 2005.
Biol Reprod 2005, 10.1095/biolreprod.105.042473
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BIOLOGY OF REPRODUCTION 73, 672–680 (2005)
DOI: 10.1095/biolreprod.105.042473
© 2005 by the Society for the Study of Reproduction, Inc.

Matrix Metalloproteinases in Endometrial Breakdown and Repair: Functional Significance in a Mouse Model1

Tu'uhevaha J. Kaitu'u 2, 3,4 , Jun Shen 3, Jin Zhang 3, Naomi B. Morison 3, and Lois A. Salamonsen 3

Prince Henry's Institute of Medical Research,3 Clayton, Victoria 3168, Australia Department of Obstetrics and Gynecology,4 Monash University, Clayton, Victoria 3168, Australia

Considerable correlative evidence suggests an important role for matrix metalloproteinases (MMPs) in menstruation, a process which occurs naturally in very few species. In this study, MMP expression was examined in a mouse model of endometrial breakdown and repair and the functional importance of MMPs determined. In the model, progesterone support was withdrawn from mice in which endometrial decidualization had been induced; 24 h later, endometrial breakdown was complete, and the entire decidual zone had been shed. Re-epithelialization had occurred by 36 h, and the endometrium had undergone extensive restoration toward a predecidualized state by 48 h. Immunoreactive MMP9 and MMP7 colocalized with leukocyte subsets, particularly neutrophils, whereas MMP13 staining was always extracellular. MMP3 and MMP7 were abundant during re-epithelialization in close proximity to newly reforming epithelium. The functional importance of MMPs in these processes was examined using two MMP inhibitors, doxycycline and batimistat. Both inhibitors effectively reduced MMP activity, as assessed by in situ zymography, but did not have significant effects on endometrial breakdown or repair. This study demonstrates that although MMPs are present in abundance during endometrial breakdown and repair in this mouse model, they are not the key mediators of these processes.

female reproductive tract, decidua, menstrual cycle, progesterone, uterus


1 Supported by the National Health and Medical Research Council of Australia (169003, 143798, 241000) and by an Australian Postgraduate Scholarship to T.J.K.

2 Correspondence: T.J. Kaitu'u, Prince Henry's Institute of Medical Research, Level 4, Block E, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria 3168, Australia. FAX: 61 3 9594 6125; tuuhevaha.kaituu{at}phimr.monash.edu.au




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