Expression of Endothelial NO Synthase, Inducible NO Synthase, and Estrogen Receptors Alpha and Beta in Placental Tissue of Normal, Preeclamptic, and Intrauterine Growth-restricted Pregnancies

• Published in: The journal of histochemistry and cytochemistry Vol. 53; no. 12; pp. 1441 - 1449
• Main Authors: Schiessl, Barbara, Mylonas, Ioannis, Hantschmann, Peer, Kuhn, Christina, Schulze, Sandra, Kunze, Susi, Friese, Klaus, Jeschke, Udo
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA Histochemical Soc 01.12.2005; SAGE Publications
• Subjects: Blotting, Western; Estrogen Receptor alpha - biosynthesis; Estrogen Receptor beta - biosynthesis; Female; Fetal Growth Retardation - metabolism; Humans; Immunohistochemistry; Nitric Oxide Synthase Type II - biosynthesis; Nitric Oxide Synthase Type III - biosynthesis; Placenta - metabolism; Pre-Eclampsia - metabolism; Pregnancy; estrogen receptor alpha/beta; intrauterine growth restriction; nitric oxide synthases; preeclampsia
• ISSN: 0022-1554; 1551-5044
• DOI: 10.1369/jhc.4A6480.2005

In the physiology of placental blood circulation, nitric oxide (NO) synthases seem to play important roles, although their expression in pathological placentas and their role is still unclear. In addition, NO synthase activation seems to be related to estrogen receptor expression. Therefore, the aims of this study were to investigate the expression of estrogen receptors alpha (ERα), estrogen receptor beta (ER and the endothelial NO synthase (eNOS), and inducible NO synthase (iNOS) in intrauterine growth-restricted (IUGR) placentas, preeclamptic placentas, and in normal healthy control placentas. Slides of paraffin-embedded placental tissue were obtained after delivery from patients diagnosed with IUGR, preeclampsia, and normal term placentas and analyzed for eNOS, iNOS as well as ERα and ERβ expression. Intensity of immunohistochemical reaction was analyzed using a semiquantitative score and statistical analysis was performed. In addition, Western blot experiments were performed for comparison of staining intensities obtained by immunohis-tochemistry and western blot. Expression of eNOS, iNOS, and ERβ is significantly reduced in trophoblast cells of placentas with IUGR. However, preeclamptic placentas demonstrated a significant elevated expression intensity of these proteins compared with normal controls. A different expression of eNOS, iNOS, ERα, and ERβ by human trophoblast cells seems to results in lower NO output and impaired trophoblast invasion. Results obtained in our study provide evidence that reduced expression of the investigated proteins is related to IUGR.