dc.creator | Riquelme Pino, Gloria | |
dc.creator | Llanos Vidal, Paola | |
dc.creator | Tischner, Erin | |
dc.creator | Neil, Jessica | |
dc.creator | Campos, Begoña | |
dc.date.accessioned | 2007-05-07T19:20:29Z | |
dc.date.accessioned | 2019-04-25T23:57:33Z | |
dc.date.available | 2007-05-07T19:20:29Z | |
dc.date.available | 2019-04-25T23:57:33Z | |
dc.date.created | 2007-05-07T19:20:29Z | |
dc.date.issued | 2004-11-26 | |
dc.identifier | JOURNAL OF BIOLOGICAL CHEMISTRY 279 (48): 50601-50608 NOV 26 2004 | |
dc.identifier | 0021-9258 | |
dc.identifier | http://repositorio.uchile.cl/handle/2250/127129 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/2431451 | |
dc.description.abstract | The syncytiotrophoblast separates the maternal and fetal blood and constitutes the primary barrier for maternal-fetal transport. The Maxi-chloride channel from the apical membrane of the syncytiotrophoblast plays a role in the chloride conductance. Annexins can play an important role in the regulation of membrane events. In this study we evaluate the role of annexin 6 in the Maxichloride channel properties. The results showed that annexin 6 is bound in the apical placenta membranes in a calcium-dependent phospholipid-binding manner but also in a calcium-independent fashion. The neutralization of annexin 6 decreased the total current by 39 +/- 1.9% in the range of +/- 80 mV, and the currents decrease with the time. The single-channel slope conductance was decreased from 253 +/- 7.4 pS ( control) to 105 +/- 13 pS, and the amplitude decreased by 50%. The open probability was also affected when higher voltage steps were used, changes in either the positive or negative direction induced the channel to close, and the open probability (P-o) did not decrease. In channels with neutralized annexin 6, it was maintained at 1 at +/- 40 mV and at +/- 80 mV. These results suggest that endogenous annexin 6 could regulate the Maxi-chloride channel. The results obtained with normal placentae, in which annexin 6 was neutralized, are similar to those described for the Maxichloride channel isolated from pre-eclamptic placenta. Together these data suggest that annexin 6 could play an important role in ion transport of the placenta. | |
dc.language | en | |
dc.publisher | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | |
dc.subject | DEPENDENT ANION CHANNEL | |
dc.title | Annexin 6 modulates the maxi-chloride channel of the apical membrane of syncytiotrophoblast isolated from human placenta | |
dc.type | Artículos de revistas | |