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Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain

Aquaporins (AQPs) facilitate water diffusion through the plasma membrane. Brain aquaporin-4 (AQP4) is present in astrocytes and has critical roles in normal and disease physiology. We previously showed that a 24.9% decrease in AQP4 expression after in vivo silencing resulted in a 45.8% decrease in t...

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Autores principales: Jullienne, Amandine, Fukuda, Andrew M., Ichkova, Aleksandra, Nishiyama, Nina, Aussudre, Justine, Obenaus, André, Badaut, Jérôme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843607/
https://www.ncbi.nlm.nih.gov/pubmed/29520011
http://dx.doi.org/10.1038/s41598-018-22268-y
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author Jullienne, Amandine
Fukuda, Andrew M.
Ichkova, Aleksandra
Nishiyama, Nina
Aussudre, Justine
Obenaus, André
Badaut, Jérôme
author_facet Jullienne, Amandine
Fukuda, Andrew M.
Ichkova, Aleksandra
Nishiyama, Nina
Aussudre, Justine
Obenaus, André
Badaut, Jérôme
author_sort Jullienne, Amandine
collection PubMed
description Aquaporins (AQPs) facilitate water diffusion through the plasma membrane. Brain aquaporin-4 (AQP4) is present in astrocytes and has critical roles in normal and disease physiology. We previously showed that a 24.9% decrease in AQP4 expression after in vivo silencing resulted in a 45.8% decrease in tissue water mobility as interpreted from magnetic resonance imaging apparent diffusion coefficients (ADC). Similar to previous in vitro studies we show decreased expression of the gap junction protein connexin 43 (Cx43) in vivo after intracortical injection of siAQP4 in the rat. Moreover, siAQP4 induced a loss of dye-coupling between astrocytes in vitro, further demonstrating its effect on gap junctions. In contrast, silencing of Cx43 did not alter the level of AQP4 or water mobility (ADC) in the brain. We hypothesized that siAQP4 has off-target effects on Cx43 expression via modification of miRNA expression. The decreased expression of Cx43 in siAQP4-treated animals was associated with up-regulation of miR224, which is known to target AQP4 and Cx43 expression. This could be one potential molecular mechanism responsible for the effect of siAQP4 on Cx43 expression, and the resultant decrease in astrocyte connectivity and dramatic effects on ADC values and water mobility.
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spelling pubmed-58436072018-03-14 Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain Jullienne, Amandine Fukuda, Andrew M. Ichkova, Aleksandra Nishiyama, Nina Aussudre, Justine Obenaus, André Badaut, Jérôme Sci Rep Article Aquaporins (AQPs) facilitate water diffusion through the plasma membrane. Brain aquaporin-4 (AQP4) is present in astrocytes and has critical roles in normal and disease physiology. We previously showed that a 24.9% decrease in AQP4 expression after in vivo silencing resulted in a 45.8% decrease in tissue water mobility as interpreted from magnetic resonance imaging apparent diffusion coefficients (ADC). Similar to previous in vitro studies we show decreased expression of the gap junction protein connexin 43 (Cx43) in vivo after intracortical injection of siAQP4 in the rat. Moreover, siAQP4 induced a loss of dye-coupling between astrocytes in vitro, further demonstrating its effect on gap junctions. In contrast, silencing of Cx43 did not alter the level of AQP4 or water mobility (ADC) in the brain. We hypothesized that siAQP4 has off-target effects on Cx43 expression via modification of miRNA expression. The decreased expression of Cx43 in siAQP4-treated animals was associated with up-regulation of miR224, which is known to target AQP4 and Cx43 expression. This could be one potential molecular mechanism responsible for the effect of siAQP4 on Cx43 expression, and the resultant decrease in astrocyte connectivity and dramatic effects on ADC values and water mobility. Nature Publishing Group UK 2018-03-08 /pmc/articles/PMC5843607/ /pubmed/29520011 http://dx.doi.org/10.1038/s41598-018-22268-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jullienne, Amandine
Fukuda, Andrew M.
Ichkova, Aleksandra
Nishiyama, Nina
Aussudre, Justine
Obenaus, André
Badaut, Jérôme
Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title_full Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title_fullStr Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title_full_unstemmed Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title_short Modulating the water channel AQP4 alters miRNA expression, astrocyte connectivity and water diffusion in the rodent brain
title_sort modulating the water channel aqp4 alters mirna expression, astrocyte connectivity and water diffusion in the rodent brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843607/
https://www.ncbi.nlm.nih.gov/pubmed/29520011
http://dx.doi.org/10.1038/s41598-018-22268-y
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