It is now accepted that gelatinase B (92 kd type IV collagenase) is involved in blastocyst implantation and trophoblast invasion. However, little is known about the regulation of this enzyme at the fetomaternal interface. Progesterone has been demonstrated to inhibit gelatinase B secretion from endometrial cells, myometrium, and cervical fibroblasts. Interestingly, the promotor of gelatinase B contains a progesterone-responsive element that may explain transcriptional activation of this metalloproteinase by progesterone. It may be hypothesized that progesterone secreted from trophoblast cells, representing the fetal part of the fetomaternal interface, may have a role in the regulation of gelatinase secretion and blastocyst implantation.
Study Design
To this end, use was made of first-trimester trophoblast cells obtained from first-trimester pregnancy terminations. The trophoblast cells were separated by trypsin degradation and fractionation on Percoll gradients. Metalloproteinase activity was measured by zymography, and the expression of the gelatinase B messenger ribonucleic acid was determined by the solution hybridization/ribonuclease protection assay.
Results
Primary cell cultures of trophoblasts from first trimesters of pregnancy constitutively elaborated two species of type IV collagenases (gelatinase A and B) as assessed on a gelatin matrix. Treatment with progesterone decreased the accumulation of a gelatinase B species in a dose-dependent fashion. Administration of a progesterone receptor antagonist onapristone (ZK-98.299) neutralized the progesterone inhibitory effect on the gelatinase B in a dose-dependent fashion, thus supporting the presumption that the progesterone effect is receptor mediated. Progesterone significantly attenuated the expression of gelatinase B by trophoblast cells, an effect that was neutralized by ZK-98.299.
Conclusion
These observations provide strong indirect support for the participation of progesterone in the regulation of gelatinase B in trophoblast cells. It may be an important regulator of gelatinase production at the fetomaternal interface.
PMID 9539508 9539508 DOI 10.1016/s0002-9378(98)70420-x 10.1016/s0002-9378(98)70420-x
Cite this article
Shimonovitz, S., Hurwitz, A., Hochner-Celnikier, D., Dushnik, M., Anteby, E., & Yagel, S. (1998). Expression of gelatinase B by trophoblast cells: down-regulation by progesterone. *American journal of obstetrics and gynecology*, *178*(3), 457-461. https://doi.org/10.1016/s0002-9378(98)70420-x
Shimonovitz S, Hurwitz A, Hochner-Celnikier D, Dushnik M, Anteby E, Yagel S. Expression of gelatinase B by trophoblast cells: down-regulation by progesterone. Am J Obstet Gynecol. 1998;178(3):457-461. doi:10.1016/s0002-9378(98)70420-x
Shimonovitz, S., et al. "Expression of gelatinase B by trophoblast cells: down-regulation by progesterone." *American journal of obstetrics and gynecology*, vol. 178, no. 3, 1998, pp. 457-461.
Valenti M et al., 2026American journal of obstetrics and gynecology
Background: Endometriosis is a chronic, gynecologic condition in which tissue similar to the lining of the uterus implants throughout the body. Women with endometriosis have a higher prevalence of inf...
Bujold E et al., 2026American Journal of Obstetrics and Gynecology
Normal uterine function depends on cyclical regeneration and the capacity to sustain pregnancy. A cesarean incision represents an injury to this remarkable organ. Although the uterus possesses excepti...
Froeliger A et al., 2024American Journal of Obstetrics and Gynecology
Background: Very little is known about the prevalence and risk factors of postpartum depression among women with vaginal births without major pregnancy complications.
Objective: This study aimed to a...
Suresh S et al., 2023American Journal of Obstetrics and Gynecology
Background: Spontaneous preterm birth significantly increases the risk for a recurrent preterm birth. Only a few identifiable clinical risk factors can be referenced in counseling for recurrent preter...