Back to Search
Start Over
MicroRNA-155 inhibits migration of trophoblast cells and contributes to the pathogenesis of severe preeclampsia by regulating endothelial nitric oxide synthase
- Source :
- Molecular medicine reports. 10(1)
- Publication Year :
- 2013
-
Abstract
- The aim of the present study was to characterize the role of microRNA (miR)-155 in the pathogenesis of severe preeclampsia (PE). A total of 19 severe preeclampsic and 22 normal placentas were collected to measure miR-155 and endothelial nitric oxide synthase (eNOS) expression using quantitative (q)PCR and western blot analysis. The results demonstrated a significant increase in the levels of miR-155 and decreased eNOS expression in the severe preeclampsic placentas, as compared with the normal controls. In order to examine the function of miR-155 in the human placenta, the HTR8/Svneo cell line was transiently transfected with an miR-155 mimic or its inhibitor, anti-miR-155. It was confirmed that miR-155 may suppress the expression of eNOS in HTR-8/SVneo cells. Furthermore, a transwell insert invasion assay demonstrated that miR-155 inhibited cell invasion in trophoblast cells, and the effect was rescued by over expression of eNOS. The present study revealed that miR-155 has a negative regulatory role in the migratory behavior of HTR-8/SVneo cells via modulating eNOS.
- Subjects :
- Adult
Cancer Research
Nitric Oxide Synthase Type III
Placenta
Cell
Biology
Biochemistry
Cell Line
Western blot
Downregulation and upregulation
Pre-Eclampsia
Enos
Cell Movement
Pregnancy
Genetics
medicine
Humans
RNA, Small Interfering
Molecular Biology
Oncogene
medicine.diagnostic_test
Trophoblast
Transfection
Oligonucleotides, Antisense
biology.organism_classification
Cell biology
Trophoblasts
Up-Regulation
MicroRNAs
medicine.anatomical_structure
Oncology
Cell culture
Molecular Medicine
Female
RNA Interference
Subjects
Details
- ISSN :
- 17913004
- Volume :
- 10
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Molecular medicine reports
- Accession number :
- edsair.doi.dedup.....38275da9995554d600d51432d4e335a8