Authors: R. Pilka 1; Milan Kudela 1; S. Hansson 2; B. Casslén 2 Authors‘ workplace: Gynekologicko-porodnická klinika, FN a LF UP, Olomouc, přednosta prof. MUDr. M. Kudela, CSc. 2Gynekologicko-porodnická klinika a Biomedicínské centrum, Univerzita Lund, Švédsko 1 Published in: Ceska Gynekol 2004; (6): 0 Category:
Objective: To examine possible estrogen dependent endometrial expression of MMP-26 in vitro.Design: Experimental study.Setting: Department of Obstetrics and Gynecology of the Palacky University Medical School andUniversity Hospital, Olomouc, Czech Republic, Department of Obstetrics and Gynecology, UniversityHospital, Lund, Sweden.Methods: We studied MMP-26 mRNA in 14 normal endometrial samples obtained from the proliferativephase of the menstrual cycle. Samples were cultured for fi ve days either with estradiolalone or in combination with progesterone. Samples cultured with ethanol represented controlgroups. MMP-26 mRNA expression was examined in frozen samples using in situ hybridization.Immunohistochemistry was used to study the presence of estrogen and progesterone receptorsin endometrial explants.Results: MMP-26 mRNA expression was highest in fresh (non cultured) samples. Signal intensitydecreased during the fi rst two days of culture and was negligable in the following days. Nuclearintensity for estrogen and progesterone receptor was high after fi ve days of culture.Conclusion: We did not fi nd MMP-26 mRNA in vitro expression to be directly estrogen dependent.
Key words: endometrium, in vitro, MMP, mRNA, regulation
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