|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Abstract
Matrix metalloproteinases (MMPs) are instrumental in the
constant tissue remodeling in the ovary. An induction of
MMP-19 mRNA in periovulatory follicles has been reported
in mouse ovaries. However, little is known about MMP-19
expression during the follicular and luteal period, or
about the ovarian regulation of MMP-19 mRNA expression.
We examined the expression pattern of MMP-19 mRNA during
various reproductive phases and the periovulatory
regulation of MMP-19 mRNA in the rat ovary. In
gonadotropin-primed immature rat ovaries, levels of MMP-
19 mRNA transiently increased during both follicular
growth and ovulation. MMP-19 mRNA was localized to the
theca-interstitial layer of growing follicles and to the
granulosa and theca-interstitial layer of periovulatory
follicles. A similar expression pattern of MMP-19 mRNA
in periovulatory follicles was observed in ovaries from
naturally cycling adult rats. Accumulation of MMP-19
mRNA was detected in regressing CL. The regulation of
MMP-19 mRNA expression during the periovulatory period
was investigated via in vivo studies and through in vitro
culture studies on follicular cells. The hCG-induction
of MMP-19 mRNA was mimicked by treating granulosa cells,
but not theca-interstitial cells, from preovulatory
follicles with LH or activators of the PKA or PKC
pathways. Cyclohexamide blocked the LH or forskolin-
induced MMP-19 mRNA expression, demonstrating the
requirement for new protein synthesis. In contrast,
blocking the activation of the progesterone receptor or
prostaglandin synthesis had no effect on the increase in
MMP-19 mRNA expression. In conclusion, the induction of
MMP-19 mRNA suggests an important role of this proteinase
during follicular growth, ovulation, and luteal
regression.
Key words:
Ovary
Corpus luteum
Follicle-stimulating hormone
Luteinizing hormone
Ovulation
This article has been cited by other articles:
![]() |
L. L Espey, R. A Garcia, H. Kondo, B. Ishizuka, S. Yoshioka, S. Fujii, S. Hampton, and J. S Richards Expression of paralogs of cytochrome P45021a1 pseudogene (Cyp21a1-ps) and endogenous retrovirus SC1 (SC1) in the rat ovary during the ovulatory process J. Endocrinol., July 1, 2008; 198(1): 231 - 241. [Abstract] [Full Text] [PDF] |
||||
![]() |
H Kliem, H Welter, W D Kraetzl, M Steffl, H H D Meyer, D Schams, and B Berisha Expression and localisation of extracellular matrix degrading proteases and their inhibitors during the oestrous cycle and after induced luteolysis in the bovine corpus luteum Reproduction, September 1, 2007; 134(3): 535 - 547. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Russell and R. L. Robker Molecular mechanisms of ovulation: co-ordination through the cumulus complex Hum. Reprod. Update, May 1, 2007; 13(3): 289 - 312. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. C Woods and A L Johnson Protein kinase C activity mediates LH-induced ErbB/Erk signaling in differentiated hen granulosa cells Reproduction, April 1, 2007; 133(4): 733 - 741. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. P. Hall, F. R. Westwood, and P. F. Wadsworth Review of the Effects of Anti-Angiogenic Compounds on the Epiphyseal Growth Plate Toxicol Pathol, February 1, 2006; 34(2): 131 - 147. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. X. Donadeu and M. Ascoli The Differential Effects of the Gonadotropin Receptors on Aromatase Expression in Primary Cultures of Immature Rat Granulosa Cells Are Highly Dependent on the Density of Receptors Expressed and the Activation of the Inositol Phosphate Cascade Endocrinology, September 1, 2005; 146(9): 3907 - 3916. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Ogiwara, N. Takano, M. Shinohara, M. Murakami, and T. Takahashi Gelatinase A and membrane-type matrix metalloproteinases 1 and 2 are responsible for follicle rupture during ovulation in the medaka PNAS, June 14, 2005; 102(24): 8442 - 8447. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |