Evidence map›Paper›PMID 29565042›Full record

ArticleMolecular psychiatry2018

Astrocytic water channel aquaporin-4 modulates brain plasticity in both mice and humans: a potential gliogenetic mechanism underlying language-associated learning.

J Woo, J E Kim, J J Im, J Lee, H S Jeong, S Park, S-Y Jung, H An, S Yoon, S M Lim and 13 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 47 citations in OpenAlex.

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  4. Influence of an AQP4 haplotype and sleep duration on early Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 8 institutions in 2 countries.

J WooCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
J E KimDepartment of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Republic of Korea.
J J ImEwha Brain Institute, Ewha Womans University, Seoul, Republic of Korea.
J LeeCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
H S JeongDepartment of Radiology, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
S ParkCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
S-Y JungCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
H AnCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
S YoonEwha Brain Institute, Ewha Womans University, Seoul, Republic of Korea.
S M LimDepartment of Radiology, College of Medicine, Ewha Womans University, Seoul, Republic of Korea.
S LeeEwha Brain Institute, Ewha Womans University, Seoul, Republic of Korea.
J MaEwha Brain Institute, Ewha Womans University, Seoul, Republic of Korea.
E Y ShinDepartment of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Republic of Korea.
Y-E HanCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
B KimEwha Brain Institute, Ewha Womans University, Seoul, Republic of Korea.
E H LeeGreen Cross Laboratories, Yongin, Republic of Korea.
L FengCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
H ChunCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
B-E YoonCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
I KangDepartment of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Republic of Korea.
S R DagerDepartment of Radiology, University of Washington, Seattle, WA, USA.
I K LyooDepartment of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Republic of Korea.
C J LeeCenter for Neural Science and Functional Connectomics, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
Korea Institute of Science and Technology · KREwha Womans University · KRSeoul National University · KRUniversity of Washington · USCatholic University of Korea · KRDankook University · KRGreen Cross (South Korea) · KRKorea University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of astrocytes in brain plasticity has not been extensively studied compared with that of neurons. Here we adopted integrative translational and reverse-translational approaches to explore the role of an astrocyte-specific major water channel in the brain, aquaporin-4 (AQP4), in brain plasticity and learning. We initially identified the most prevalent genetic variant of AQP4 (single nucleotide polymorphism of rs162008 with C or T variation, which has a minor allele frequency of 0.21) from a human database (n=60 706) and examined its functionality in modulating the expression level of AQP4 in an in vitro luciferase reporter assay. In the following experiments, AQP4 knock-down in mice not only impaired hippocampal volumetric plasticity after exposure to enriched environment but also caused loss of long-term potentiation after theta-burst stimulation. In humans, there was a cross-sectional association of rs162008 with gray matter (GM) volume variation in cortices, including the vicinity of the Perisylvian heteromodal language area (Sample 1, n=650). GM volume variation in these brain regions was positively associated with the semantic verbal fluency. In a prospective follow-up study (Sample 2, n=45), the effects of an intensive 5-week foreign language (English) learning experience on regional GM volume increase were modulated by this AQP4 variant, which was also associated with verbal learning capacity change. We then delineated in mice mechanisms that included AQP4-dependent transient astrocytic volume changes and astrocytic structural elaboration. We believe our study provides the first integrative evidence for a gliogenetic basis that involves AQP4, underlying language-associated brain plasticity.

Indexed as

Language DevelopmentAdultAnimalsAquaporin 4AstrocytesBrainCross-Sectional StudiesDisease Models, AnimalFemaleFollow-Up StudiesGene FrequencyGray MatterHippocampusHumansLearningMaleAQP4 protein, humanAqp4 protein, mouseAquaporin 4

Identifiers

PMID29565042
OpenAlexW2659271799

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.