Evidence map›Paper›PMID 25432888›Full record

ArticleMolecular neurobiology2016

Lack of JWA Enhances Neurogenesis and Long-Term Potentiation in Hippocampal Dentate Gyrus Leading to Spatial Cognitive Potentiation.

Sha Sha, Jin Xu, Zi-Hong Lu, Juan Hong, Wei-Jun Qu, Jian-Wei Zhou, Ling Chen

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
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  4. Glutathione in the Brain.International journal of molecular sciences · 2021
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Sha ShaLaboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, Jiangsu, 210029, China.
Jin XuDepartment of Molecular Cell Biology and Toxicology, School of Public Health, Nanjing Medical University, Hanzhong Road 140, Nanjing, Jiangsu, 210029, China.
Zi-Hong LuDepartment of Physiology, Nanjing Medical University, Hanzhong Road 140, Nanjing, Jiangsu, 210029, China.
Juan HongDepartment of Physiology, Nanjing Medical University, Hanzhong Road 140, Nanjing, Jiangsu, 210029, China.
Wei-Jun QuDepartment of Physiology, Nanjing Medical University, Hanzhong Road 140, Nanjing, Jiangsu, 210029, China.
Jian-Wei ZhouDepartment of Molecular Cell Biology and Toxicology, School of Public Health, Nanjing Medical University, Hanzhong Road 140, Nanjing, Jiangsu, 210029, China. jwzhou@njmu.edu.cn.
Ling ChenLaboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, Jiangsu, 210029, China. lingchen@njmu.edu.cn.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

JWA (Arl6ip5), a homologous gene of glutamate-transporter-associated protein 3-18 (GTRAP3-18) and addicsin, is highly expressed in hippocampus. We generated systemic and neuronal JWA knockout (JWA-KO and JWA-nKO) mice to investigate the influence of JWA deficiency on spatial cognitive performance, process of neurogenesis, and induction of long-term potentiation (LTP) in hippocampal dentate gyrus (DG). In comparison with wild-type (WT) mice and JWA (loxP/loxP) (control of JWA-nKO) mice, 8-week-old JWA-KO mice and JWA-nKO mice showed spatial cognitive potentiation as assessed by Morris water maze test. In hippocampal DG of JWA-nKO mice, either survival and migration or neurite growth of newborn neurons were significantly enhanced without the changes in proliferation and differentiation of stem cells. In addition, the increase of LTP amplitude and the decline of LTP threshold were observed in DG, but not in CA1 region, of JWA-nKO mice compared to control mice. The levels of hippocampal FAK, Akt, and mTOR phosphorylation in JWA-nKO mice were higher than those in control mice. The PI3K or FAK inhibitor could abolish the enhanced neurogenesis and LTP induction in JWA-nKO mice, which was accompanied by disappearance of the spatial cognitive potentiation. The treatment of JWA-nKO mice with 3'-azido-3'-deoxythymidine (AZT), a telomerase inhibitor, suppressed not only the enhanced neurogenesis but also the enhanced LTP induction in DG, but it did not affect the LTP induction in CA1 region. The results suggest that the JWA deficiency through cascading FAK-PI3K-Akt-mTOR pathway increases the newborn neurons and enhances the LTP induction in hippocampal DG, which leads to the spatial cognitive potentiation.

Indexed as

CognitionLong-Term PotentiationNeurogenesisAnimalsAnimals, NewbornCarrier ProteinsCell MovementCell SurvivalDentate GyrusFocal Adhesion Protein-Tyrosine KinasesGenotypeHeat-Shock ProteinsMembrane Transport ProteinsMice, KnockoutNeuritesPhosphorylationArl6ip5 protein, mouseCarrier ProteinsFocal Adhesion Protein-Tyrosine KinasesHeat-Shock ProteinsMembrane Transport ProteinsProtein Kinase InhibitorsProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesZidovudineHippocampusJWALong-term potentiation (LTP)MemoryNeurogenesis

Identifiers

PMID25432888
OpenAlexW2087619478

What OpenQuestion holds

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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.