Change profiles in matrix metalloproteinase-2 and -9 in induced endometriosis in mice

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In induced endometriosis in mice, MMP-2 and MMP-9 mRNA, protein levels, and activities significantly increased after induction, with MMP-9 showing multiple peaks over 21 days.

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The paper investigated how matrix metalloproteinase-2 and -9 (MMP-2, MMP-9) change during the development and progression of induced endometriosis in mice by measuring MMP mRNA (real-time quantitative PCR), protein levels (ELISA), and enzymatic activity (gelatin zymography) in experimental versus sham-operated control animals from day 1 to day 21. MMP-2 and MMP-9 mRNA, protein, and activity were significantly increased on day 1 after induction, with MMP-2 remaining higher than controls throughout the observation period. MMP-9 showed multiple activity peaks at day 1, day 4, and day 15. The paper concludes these MMP alterations may be involved in endometriosis pathogenesis but does not provide mechanistic causality beyond correlative expression/activity changes in this specific mouse model. This paper is centrally about endometriosis — it specifically profiles MMP-2 and MMP-9 expression and activity across time after induction of endometriosis in mice.

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Summary To examine the changes in matrix metalloproteinase-2 (MMP-2) and -9 (MMP-9) in the development and progression of endometriosis, real time quantitative polymerase chain reaction, enzyme-linked immunoabsorbent assay and gelatin zymography were employed to determine the mRNA and protein levels and activities of MMP-2 and MMP-9 from the first day to the 21st day after the induction in mice with induced endometriosis (experimental group) and sham-operated animals (controls). The results showed that the mRNA and protein levels and activities of the MMP-2 and MMP-9 were significantly increased on the first day after the induction and the level of MMP-2 stayed at a level higher than that in the control group. MMP-9 had two or three peaks during the 21 days, taking place at day 1, 4 and 15. It is concluded that the changes in the MMP-2 and MMP-9 might be involved in pathogenesis of endometriosis. Similar content being viewed by others References Chen QH, Qu JY, Xu YY, et al. Expressions of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in ectopic and eutopic endometrium. Chin J Obstet Gynecol (Chinese), 2004,39(12):809–812 Li T, Li YG, Pu DM. Matrix metalloproteinase-2 and -9 expression correlated with angiogenesis in human adenomyosis. Gynecol Obstet Invest 2006, 62: 229–35. Vincent Lagente, Elisabeth Boichot. Matrix metallo-proteinases in tissue remodelliing and inflammation. In: Gasche Y, Copin JC. Matrix metalloproteinases and inflammatory diseases of the central nervous system. Germany Berlin: Die Deutche Bibliothek, 2008:123–152 Chen QH, Zhou WD, Pu DM, et al. The inhibitory effect of 15-R-LXA4 on experimental endometriosis. EJOG, 2009,145(2):200–204 Cao ZY. Chinese Gynecology and Obstetrics. In: Gao Y. Pathology of Ectopic Endometrium. Beijing: People’s Medical Publishing House, 2004,1486–1488 Lang JH. Researches and hypostheses on ectopic endometrium. Chin J Obstet Gynecol (Chinese), 2003, 38(8):478–480 Sternlicht M, Werb Z. How matrix metalloproteinases regulate cell behavior. Annu Rev Cell Dev Biol, 2001,17: 463–516 Gilabert-Estellés J, Ramón LA, España F, et al. Expression of angiogenic factors in endometriosis: relationship to fibrinolytic and metalloproteinase systems. Hum Reprod, 2007,22(8):2120–2127 Chen QH, Zhou WD, Su ZY, et al. Change of pro-inflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model. Fertil Steril, 2010,93(5):1448–1454 Parks WC, Wilson C, Lopez-Boado YS. Matrix metalloproteinases as modulators of inflammation and innate immunity. Nat Rev Immunol, 2004,4(8):617–629 Mulayim N, Savlu A, Guzeloglu-Kayisli O, et al. Regulation of endometrial stromal cell matrix metalloproteinase activity and invasiveness by interleukin-8. Fertil Steril, 2004,81(Suppl 1):904–911 Man YC, Liu Y, Xie W, et al. Effect of blockage of Wnt/β-catenin signaling pathway on activation eutopic endometrial stromal cell of patients with endometriosis by 17β-estradiol treatment. Acta Med Univ Sci Technol Huazhong (Chinese), 2009,38(4):421–424,429 Mott JD, Werb Z. Regulation of matrix biology by matrix metalloproteinases. Curr Opin Cell Biol, 2004,16(5): 558–564 Author information Authors and Affiliations Corresponding author Additional information This project was supported by grants from Xiamen Municipal Scientific Research Program (No. 3502 Z 20077047), fund for Medical Research Projects of Scientific and Technological Program (No. 3502 Z 20084006) and a medical innovation-supporting program of Fujian Province (No. 2009-CXB-49). Rights and permissions About this article Cite this article Chen, Q., Qiu, N., Pu, D. et al. Change profiles in matrix metalloproteinase-2 and -9 in induced endometriosis in mice. J. Huazhong Univ. Sci. Technol. [Med. Sci.] 30, 188–192 (2010). https://doi.org/10.1007/s11596-010-0211-4 Received: Published: Issue date: DOI: https://doi.org/10.1007/s11596-010-0211-4

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Condition tags

mesh:D004715endometriosis

MeSH descriptors

Endometriosis Matrix Metalloproteinase 2 Matrix Metalloproteinase 9 Peritoneal Diseases Animals Endometriosis Endometriosis Female Matrix Metalloproteinase 2 Matrix Metalloproteinase 2 Matrix Metalloproteinase 9 Matrix Metalloproteinase 9 Mice Mice, Inbred BALB C Peritoneal Diseases Peritoneal Diseases RNA, Messenger RNA, Messenger RNA, Messenger

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