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

Authors :
Wenyan Zou
Benjamin A. Plog
Ruth M. Castellanos Rivera
Benjamin T. Kress
Iben Lundgaard
Tinglin Pu
Yoichiro Abe
Aravind Asokan
Xiaowen Wang
Anna L.R. Xavier
Matthew J. Simon
Masato Yasui
Ting Du
Humberto Mestre
Hajime Hirase
Alexander S. Thrane
Hiromu Monai
Giridhar Murlidharan
Lauren M. Hablitz
Ming Xiao
Virginia Plá
Martin M. Pike
John H. Thomas
Weixi Feng
Jeffrey J. Iliff
Source :
eLife, eLife, Vol 7 (2018), Mestre, H, Hablitz, L M, Xavier, A L R, Feng, W, Zou, W, Pu, T, Monai, H, Murlidharan, G, Rivera, R M C, Simon, M J, Pike, M M, Pla, V, Du, T, Kress, B T, Wang, X, Plog, B A, Thrane, A S, Lundgaard, I, Abe, Y, Yasui, M, Thomas, J H, Xiao, M, Hirase, H, Asokan, A, Iliff, J J & Nedergaard, M 2018, ' Aquaporin-4-dependent glymphatic solute transport in the rodent brain ', eLife, vol. 7, :e40070 . https://doi.org/10.7554/eLife.40070
Publication Year :
2018

Abstract

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.

Details

ISSN :
2050084X
Volume :
7
Database :
OpenAIRE
Journal :
eLife
Accession number :
edsair.doi.dedup.....c6ffadb4a579883c6532d272a692b56e