» Articles » PMID: 19116037

Gelatinase (MMP-2 and -9) Expression Profiles During Gestation in the Bovine Endometrium

Overview
Publisher Biomed Central
Date 2009 Jan 1
PMID 19116037
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Various molecules participate in implantation and maintaining endometrial function during gestation. The remodeling of endometrial matrices is a necessary process in the coordination of gestational progress. Matrix-metalloproteinases (MMPs) like gelatinases (MMP-2 and -9) and collagenase (MMP-1) are considered to play important roles in this process. We examined MMP-2 and -9 expression using zymography, in situ hybridization, real-time PCR, and microarray analysis to clarify their roles in the bovine endometrium during gestation.

Methods: Endometria, placentomes, and fetal membranes were collected from Japanese black cows that were killed on day 15 to 252 of gestation or during their estrous cycle. The gene expression of MMP-related molecules (mainly MMP-2 and -9) was examined using a custom-made microarray, real-time RT-PCR, and in-situ hybridization. Gelatinase activity was detected by zymography and film in situ zymography.

Results: Both gelatinases were expressed in the endometrium and fetal tissues throughout gestation. MMP-2 gene expression declined with the progress of gestation, but its intensity was maintained at a high level during the peri-implantation period and increased in late gestation. The expression level of MMP-9 was stably maintained, but was relatively low compared to that of MMP-2. These gene expression patterns matched those detected by zymography for the proteins. Microarray analysis suggested that the functions of MMP-2 during implantation and the last part of gestation are closely related with those of other molecules such as tissue inhibitors of metalloproteinase (TIMP)-2, a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) 1, membrane type 1 (MT1)-MMP, and extracellular matrix metalloproteinase inducer (EMMPRIN).

Conclusion: We detected MMP-2 and -9 gene expression in the bovine endometrium and placentome throughout gestation. These data suggest that MMP-2 is one of the main endometrial remodeling factors for implantation and pre-partum in cattle. In cows, as is the case in humans and rodents, gelatinases participate in endometrial remodeling, and their activities depend on the balance of activators and inhibitors; i.e., TIMP, MT-MMP, EMMPRIN, MMP-2, MMP-9, and so on.

Citing Articles

Transcriptomics of -Infected Fibroblasts Reveals Hallmarks of Early Fibrosis and Cancer Progression.

Fernandez-Alvarez M, Horcajo P, Jimenez-Melendez A, Lara P, Huertas-Lopez A, Huertas-Lopez F Microorganisms. 2024; 12(3).

PMID: 38543637 PMC: 10975890. DOI: 10.3390/microorganisms12030586.


Establishment of bovine trophoblast stem cells.

Wang Y, Ming H, Yu L, Li J, Zhu L, Sun H Cell Rep. 2023; 42(5):112439.

PMID: 37146606 PMC: 10950030. DOI: 10.1016/j.celrep.2023.112439.


Reductions of Circulating Nitric Oxide are Followed by Hypertension during Pregnancy and Increased Activity of Matrix Metalloproteinases-2 and -9 in Rats.

Nascimento R, Possomato-Vieira J, Bonacio G, Rizzi E, Dias-Junior C Cells. 2019; 8(11).

PMID: 31703340 PMC: 6912623. DOI: 10.3390/cells8111402.


The increased of MMP-9 and MMP-2 with the decreased of TIMP-1 on the uterosacral ligament after childbirth.

Rahajeng R Pan Afr Med J. 2019; 30:283.

PMID: 30637068 PMC: 6317396. DOI: 10.11604/pamj.2018.30.283.9905.


Uterine influences on conceptus development in fertility-classified animals.

Moraes J, Behura S, Geary T, Hansen P, Neibergs H, Spencer T Proc Natl Acad Sci U S A. 2018; 115(8):E1749-E1758.

PMID: 29432175 PMC: 5828633. DOI: 10.1073/pnas.1721191115.


References
1.
Xu P, Wang Y, Zhu S, Luo S, Piao Y, Zhuang L . Expression of matrix metalloproteinase-2, -9, and -14, tissue inhibitors of metalloproteinase-1, and matrix proteins in human placenta during the first trimester. Biol Reprod. 2000; 62(4):988-94. DOI: 10.1095/biolreprod62.4.988. View

2.
Ohuchi E, Imai K, Fujii Y, Sato H, Seiki M, Okada Y . Membrane type 1 matrix metalloproteinase digests interstitial collagens and other extracellular matrix macromolecules. J Biol Chem. 1997; 272(4):2446-51. DOI: 10.1074/jbc.272.4.2446. View

3.
Curry Jr T, Osteen K . Cyclic changes in the matrix metalloproteinase system in the ovary and uterus. Biol Reprod. 2001; 64(5):1285-96. DOI: 10.1095/biolreprod64.5.1285. View

4.
Krussel J, Bielfeld P, Polan M, Simon C . Regulation of embryonic implantation. Eur J Obstet Gynecol Reprod Biol. 2003; 110 Suppl 1:S2-9. DOI: 10.1016/s0301-2115(03)00167-2. View

5.
Huppertz B, Kertschanska S, Demir A, Frank H, Kaufmann P . Immunohistochemistry of matrix metalloproteinases (MMP), their substrates, and their inhibitors (TIMP) during trophoblast invasion in the human placenta. Cell Tissue Res. 1998; 291(1):133-48. DOI: 10.1007/s004410050987. View