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Aquaporin-4-dependent glymphatic solute transport in the rodent brain

The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find...

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Autores principales: Mestre, Humberto, Hablitz, Lauren M, Xavier, Anna LR, Feng, Weixi, Zou, Wenyan, Pu, Tinglin, Monai, Hiromu, Murlidharan, Giridhar, Castellanos Rivera, Ruth M, Simon, Matthew J, Pike, Martin M, Plá, Virginia, Du, Ting, Kress, Benjamin T, Wang, Xiaowen, Plog, Benjamin A, Thrane, Alexander S, Lundgaard, Iben, Abe, Yoichiro, Yasui, Masato, Thomas, John H, Xiao, Ming, Hirase, Hajime, Asokan, Aravind, Iliff, Jeffrey J, Nedergaard, Maiken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307855/
https://www.ncbi.nlm.nih.gov/pubmed/30561329
http://dx.doi.org/10.7554/eLife.40070
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author Mestre, Humberto
Hablitz, Lauren M
Xavier, Anna LR
Feng, Weixi
Zou, Wenyan
Pu, Tinglin
Monai, Hiromu
Murlidharan, Giridhar
Castellanos Rivera, Ruth M
Simon, Matthew J
Pike, Martin M
Plá, Virginia
Du, Ting
Kress, Benjamin T
Wang, Xiaowen
Plog, Benjamin A
Thrane, Alexander S
Lundgaard, Iben
Abe, Yoichiro
Yasui, Masato
Thomas, John H
Xiao, Ming
Hirase, Hajime
Asokan, Aravind
Iliff, Jeffrey J
Nedergaard, Maiken
author_facet Mestre, Humberto
Hablitz, Lauren M
Xavier, Anna LR
Feng, Weixi
Zou, Wenyan
Pu, Tinglin
Monai, Hiromu
Murlidharan, Giridhar
Castellanos Rivera, Ruth M
Simon, Matthew J
Pike, Martin M
Plá, Virginia
Du, Ting
Kress, Benjamin T
Wang, Xiaowen
Plog, Benjamin A
Thrane, Alexander S
Lundgaard, Iben
Abe, Yoichiro
Yasui, Masato
Thomas, John H
Xiao, Ming
Hirase, Hajime
Asokan, Aravind
Iliff, Jeffrey J
Nedergaard, Maiken
author_sort Mestre, Humberto
collection PubMed
description The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find an effect of Aqp4 knock-out (KO) on CSF and interstitial fluid (ISF) tracer transport, five groups re-examined the importance of AQP4 in glymphatic transport. We concur that CSF influx is higher in wild-type mice than in four different Aqp4 KO lines and in one line that lacks perivascular AQP4 (Snta1 KO). Meta-analysis of all studies demonstrated a significant decrease in tracer transport in KO mice and rats compared to controls. Meta-regression indicated that anesthesia, age, and tracer delivery explain the opposing results. We also report that intrastriatal injections suppress glymphatic function. This validates the role of AQP4 and shows that glymphatic studies must avoid the use of invasive procedures.
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spelling pubmed-63078552019-01-02 Aquaporin-4-dependent glymphatic solute transport in the rodent brain Mestre, Humberto Hablitz, Lauren M Xavier, Anna LR Feng, Weixi Zou, Wenyan Pu, Tinglin Monai, Hiromu Murlidharan, Giridhar Castellanos Rivera, Ruth M Simon, Matthew J Pike, Martin M Plá, Virginia Du, Ting Kress, Benjamin T Wang, Xiaowen Plog, Benjamin A Thrane, Alexander S Lundgaard, Iben Abe, Yoichiro Yasui, Masato Thomas, John H Xiao, Ming Hirase, Hajime Asokan, Aravind Iliff, Jeffrey J Nedergaard, Maiken eLife Neuroscience The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find an effect of Aqp4 knock-out (KO) on CSF and interstitial fluid (ISF) tracer transport, five groups re-examined the importance of AQP4 in glymphatic transport. We concur that CSF influx is higher in wild-type mice than in four different Aqp4 KO lines and in one line that lacks perivascular AQP4 (Snta1 KO). Meta-analysis of all studies demonstrated a significant decrease in tracer transport in KO mice and rats compared to controls. Meta-regression indicated that anesthesia, age, and tracer delivery explain the opposing results. We also report that intrastriatal injections suppress glymphatic function. This validates the role of AQP4 and shows that glymphatic studies must avoid the use of invasive procedures. eLife Sciences Publications, Ltd 2018-12-18 /pmc/articles/PMC6307855/ /pubmed/30561329 http://dx.doi.org/10.7554/eLife.40070 Text en © 2018, Mestre et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mestre, Humberto
Hablitz, Lauren M
Xavier, Anna LR
Feng, Weixi
Zou, Wenyan
Pu, Tinglin
Monai, Hiromu
Murlidharan, Giridhar
Castellanos Rivera, Ruth M
Simon, Matthew J
Pike, Martin M
Plá, Virginia
Du, Ting
Kress, Benjamin T
Wang, Xiaowen
Plog, Benjamin A
Thrane, Alexander S
Lundgaard, Iben
Abe, Yoichiro
Yasui, Masato
Thomas, John H
Xiao, Ming
Hirase, Hajime
Asokan, Aravind
Iliff, Jeffrey J
Nedergaard, Maiken
Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title_full Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title_fullStr Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title_full_unstemmed Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title_short Aquaporin-4-dependent glymphatic solute transport in the rodent brain
title_sort aquaporin-4-dependent glymphatic solute transport in the rodent brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307855/
https://www.ncbi.nlm.nih.gov/pubmed/30561329
http://dx.doi.org/10.7554/eLife.40070
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