Oral Presentations: Basic Sciences II.
Dr. Kovács, Árpád Ferenc
Semmelweis University, Department of Genetics, Cell and Immunobiology
0036307875026
dr.arpad@yahoo.com
Emerging roles of pregnancy-associated circulating extracellular vesicles in modulation of trophoblast cell functions
Á. F. Kovács1, N. Fekete1, O. Láng1, L. Kőhidai1, J. Rigó2, L. Turiák3, E. I. Buzás1, É. Pállinger1
1 Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary
2 1st Department of Obstetrics and Gynaecology, Semmelweis University, Budapest, Hungary
3 Institute of Organic Chemistry, Hungarian Academy of Sciences, Budapest, Hungary
molecular sciences
Oral Presentations: Basic Sciences II.
Doctoral School of Molecular Medicine
Program: Basis of Human Molecular Genetics and Gene Diagnostics
Supervisor: Éva Pállinger
E-mail: eva.pallinger@gmail.com
Introduction: Extracellular vesicles (EV) represent a critically important, directed intercellular communication pathway during pregnancy. Circulating EV patterns are associated with pregnancy complications, and may exert divergent effects on target cells.
Aim: The aim of our study was to identify the effects of circulating pregnancy-associated EVs on trophoblasts, as potential target cells.
Methods: The effects of pregnancy-associated EVs were monitored by the using of BeWo choriocarcinoma cell line as a model system. EV-enriched preparations were isolated from the plasma of healthy (HP-EV) or preeclamptic pregnants (PE-EV) by differential centrifugation and were characterized by flow cytometry, dynamic light scattering, confocal laser scanning microscopy (CLSM), transmission electron microscopy and mass spectrometry. Adhesiveness and migratory activity of EV-treated BeWo cells were assessed by an impedance- based real-time method (xCELLigence SP) and by holographic microscopy (Holo Monitor M4). Trophoblast invasion and placental remodelling was examined by a wound-healing assay.
Results: Pregnancy-associated EVs isolated from each group augmented the adhesion kinetics of BeWo cells, although the effect of PE-EVs was less pronounced. Furthermore, PE-EVs induced reduced cell migration and motility. Conversely, the invasiveness of BeWo cells was intensified in the presence of PE-EVs. The differential effects of circulating EVs isolated from healthy and preeclamptic patients could be explained by their distinct protein cargos as suggested by by mass spectrometry.
Conclusion: Our in vitro experiments suggest that pregnancy-associated circulating EVs affect the invasion of trophoblast cells, which may be very important in the regulation of spiral artery remodelling and ultimately, the placentation.
Szabad
nem rendelkezett róla
1283
Á. F. Kovács1, N. Fekete1, O. Láng1, L. Kőhidai1, J. Rigó2, L. Turiák3, E. I. Buzás1, É. Pállinger1
1 Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary
2 1st Department of Obstetrics and Gynaecology, Semmelweis University, Budapest, Hungary
3 Institute of Organic Chemistry, Hungarian Academy of Sciences, Budapest, Hungary