INVESTIGADORES
IBARRA cristina Adriana
congresos y reuniones científicas
Título:
Functional expression of aquaporins in fetal membranes from human term placenta.
Autor/es:
DAMIANO A, LEVI L, ZOTTA E, IBARRA C
Lugar:
Santiago de Chile
Reunión:
Simposio; II Lati-American Symposium Materno-Fetal Interaction & Placenta: From Basic to Clinical Research; 2005
Institución organizadora:
Sociedad Latinoamericana de Placenta
Resumen:
To be absorbed into the chorionic or placental circulation, amniotic fluid water and solutes must cross the avascular amniotic membrane, probably mediated by water channels. The expression of aquaporins (AQPs) 1, 3, 8 and 9 was previously described in fetal membranes. Noteworthy, AQP9 expression is regulated by endocrine factors. We also detected AQP7 by RT-PCR and immunohistochemistry. In this study, we characterize the functional expression of AQPs and its hormonal regulation. Methods: Human fetal membrane of term placentas obtained from cesarean were dissected and immediately mounted as a diaphragm in a Ussing chamber. The net trans-epithelial water flux (Jw) was recorded minute by minute by an equipment used currently in our laboratory. Results: In amnion and chorion, a similar absortive Jw [(0.35 ± 0.05) and (0.38 ± 0.07) µL. min-1.cm-2] was observed. These Jw were increased when an osmotic gradient was generated by adding (to the maternal side) different concentrations of poly(ethylene gycol) (Mr ~ 8000). The osmotic permeability (Posm) calculated was similar in both fetal membranes [(1.6 ± 0.3) vs (1.3 ± 0.3) 10-2 cm s-1] and they were significantly decreased (P<0.05, n=6) after preincubation with 0.3 mM HgCl2. Finally Jw increased [(0.61 ± 0.06) µL min-1 cm-2, P<0.05, n=4] when chorion was cultured during 24h with 300ng/mL progesterone (P4).This is the first study that reports the functionality of the AQPs present in the human fetal membranes and its up-regulation by P4. Conclusions: These results suggest that AQPs mediate water transport across fetal membranes and the activity of AQPs is promoted by P4. This hormonal mechanism indicates a potential regulation of amniotic fluid homeostasis. ANPCYT PICT 9508/02.