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Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies

The region of the amnion overlying the placenta plays an active role in fluid exchange between amniotic fluid and fetal blood perfusing the surface of the placenta, whereas little transfer occurs across the reflected amnion that contacts the membranous chorion. Because aquaporins (AQPs) facilitate r...

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Autores principales: Bednar, Amy D, Beardall, Michael K, Brace, Robert A, Cheung, Cecilia Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393155/
https://www.ncbi.nlm.nih.gov/pubmed/25742957
http://dx.doi.org/10.14814/phy2.12320
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author Bednar, Amy D
Beardall, Michael K
Brace, Robert A
Cheung, Cecilia Y
author_facet Bednar, Amy D
Beardall, Michael K
Brace, Robert A
Cheung, Cecilia Y
author_sort Bednar, Amy D
collection PubMed
description The region of the amnion overlying the placenta plays an active role in fluid exchange between amniotic fluid and fetal blood perfusing the surface of the placenta, whereas little transfer occurs across the reflected amnion that contacts the membranous chorion. Because aquaporins (AQPs) facilitate rapid movement of water across cells, we hypothesized that AQP gene expression in placental amnion is higher than in reflected amnion. Furthermore, because gestational diabetes mellitus (GDM) is often associated with polyhydramnios, we hypothesized that amnion AQP gene expression is reduced when amniotic fluid volume is elevated. Human placental and reflected amnion were obtained at cesarean delivery and subjected to relative quantitation of AQP mRNA by real-time RT-qPCR and proteins by western immunoblot. Amnion mRNA levels of five AQPs differed by up to 400-fold (P < 0.001), with AQP1 and AQP3 most abundant, AQP8 least and AQP9 and AQP11 intermediately expressed. Aquaporin proteins showed a similar profile. Aquaporin mRNA abundance was higher (P < 0.001) in placental than reflected amnion, whereas protein levels were lower (P < 0.01). In GDM pregnancies, neither AQP mRNA nor protein levels were different from normal. There was no correlation between AQP mRNA or protein levels with the amniotic fluid index in normal or GDM subjects. We conclude that there is a strong differential expression profile among individual AQPs and between regions of the amnion. These findings suggest differences in contribution of individual AQPs to water transport in the two regions of the amnion. Furthermore, AQP expression in the amnion is not altered in patients with GDM.
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spelling pubmed-43931552015-04-20 Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies Bednar, Amy D Beardall, Michael K Brace, Robert A Cheung, Cecilia Y Physiol Rep Original Research The region of the amnion overlying the placenta plays an active role in fluid exchange between amniotic fluid and fetal blood perfusing the surface of the placenta, whereas little transfer occurs across the reflected amnion that contacts the membranous chorion. Because aquaporins (AQPs) facilitate rapid movement of water across cells, we hypothesized that AQP gene expression in placental amnion is higher than in reflected amnion. Furthermore, because gestational diabetes mellitus (GDM) is often associated with polyhydramnios, we hypothesized that amnion AQP gene expression is reduced when amniotic fluid volume is elevated. Human placental and reflected amnion were obtained at cesarean delivery and subjected to relative quantitation of AQP mRNA by real-time RT-qPCR and proteins by western immunoblot. Amnion mRNA levels of five AQPs differed by up to 400-fold (P < 0.001), with AQP1 and AQP3 most abundant, AQP8 least and AQP9 and AQP11 intermediately expressed. Aquaporin proteins showed a similar profile. Aquaporin mRNA abundance was higher (P < 0.001) in placental than reflected amnion, whereas protein levels were lower (P < 0.01). In GDM pregnancies, neither AQP mRNA nor protein levels were different from normal. There was no correlation between AQP mRNA or protein levels with the amniotic fluid index in normal or GDM subjects. We conclude that there is a strong differential expression profile among individual AQPs and between regions of the amnion. These findings suggest differences in contribution of individual AQPs to water transport in the two regions of the amnion. Furthermore, AQP expression in the amnion is not altered in patients with GDM. BlackWell Publishing Ltd 2015-03-05 /pmc/articles/PMC4393155/ /pubmed/25742957 http://dx.doi.org/10.14814/phy2.12320 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Bednar, Amy D
Beardall, Michael K
Brace, Robert A
Cheung, Cecilia Y
Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title_full Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title_fullStr Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title_full_unstemmed Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title_short Differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
title_sort differential expression and regional distribution of aquaporins in amnion of normal and gestational diabetic pregnancies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393155/
https://www.ncbi.nlm.nih.gov/pubmed/25742957
http://dx.doi.org/10.14814/phy2.12320
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