| Literature DB >> 30561329 |
Humberto Mestre1, Lauren M Hablitz1, Anna Lr Xavier2, Weixi Feng3, Wenyan Zou3, Tinglin Pu3, Hiromu Monai4,5, Giridhar Murlidharan6, Ruth M Castellanos Rivera6, Matthew J Simon7, Martin M Pike8, Virginia Plá1, Ting Du1, Benjamin T Kress1, Xiaowen Wang4, Benjamin A Plog1, Alexander S Thrane2,9, Iben Lundgaard1,10,11, Yoichiro Abe12, Masato Yasui12, John H Thomas13,14, Ming Xiao3, Hajime Hirase4,15, Aravind Asokan6,16,17, Jeffrey J Iliff7,18, Maiken Nedergaard1,2.
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.Entities:
Keywords: aquaporin-4; cerebrospinal fluid; glymphatic; meta-analysis; mouse; neuroscience; replication study; solute transport
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Year: 2018 PMID: 30561329 PMCID: PMC6307855 DOI: 10.7554/eLife.40070
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140