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Regulation and Function of LEFTY-A/EBAF in the Human Endometrium. mRNA Expression During the Menstrual Cycle, Control By Progesterone, and Effect on Matrix Metalloproteinases

The human endometrium is a unique tissue that is periodically shed during menstruation. Although overall triggered by ovarian steroids withdrawal, menstrual induction of matrix metalloproteinases (MMPs) and resulting tissue breakdown are focal responses, pointing to additional local modulators. LEFT...

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Bibliographic Details
Published in:The Journal of biological chemistry 2002-11, Vol.277 (45), p.42496-42504
Main Authors: Cornet, P B, Picquet, C, Lemoine, P, Osteen, K G, Bruner-Tran, K L, Tabibzadeh, S, Courtoy, P J, Eeckhout, Y, Marbaix, E, Henriet, P
Format: Article
Language:English
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Summary:The human endometrium is a unique tissue that is periodically shed during menstruation. Although overall triggered by ovarian steroids withdrawal, menstrual induction of matrix metalloproteinases (MMPs) and resulting tissue breakdown are focal responses, pointing to additional local modulators. LEFTY-A, a novel member of the transforming growth factor-[beta] family identified originally as an endometrial bleeding-associated factor (EBAF), is a candidate for this local control. We measured LEFTY-A and [beta]-ACTIN mRNA concentration during the menstrual cycle in vivo and found that their ratio was dramatically (100-fold) increased at the perimenstrual phase. A similar increase was seen when proliferative explants were cultured for 24 h in the absence of ovarian steroids; this was followed by spontaneous production of proMMP-1, -3, and -9. Both responses were inhibited by progesterone. Moreover, addition of recombinant LEFTY-A to proliferative explants was sufficient to stimulate the expression of proMMP-3 and -7; this response was also blocked by ovarian steroids. Collectively, these data indicate that LEFTY-A may provide a crucial signal for endometrial breakdown and bleeding by triggering expression of several MMPs. Progesterone appears to exert a dual block, upstream by inhibiting LEFTY-A expression and downstream by suppressing its stimulatory effect on MMPs.
ISSN:0021-9258
DOI:10.1074/jbc.M201793200