Evidence map›Paper›PMID 31166939›Full record

ArticlePLoS biology2019

NGL-3 in the regulation of brain development, Akt/GSK3b signaling, long-term depression, and locomotive and cognitive behaviors.

Hyejin Lee, Wangyong Shin, Kyungdeok Kim, Suho Lee, Eun-Jae Lee, Jihye Kim, Hanseul Kweon, Eunee Lee, Haram Park, Muwon Kang and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Cell Adhesion Molecule Signaling at the Synapse: Beyond the Scaffold.Cold Spring Harbor perspectives in biology · 2024
    Review
  5. Article
  6. Article
  7. Molecular mechanisms of synaptogenesis.Frontiers in synaptic neuroscience · 2022
    Review
  8. Article
  9. Article
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

13 authors at 4 institutions in 1 country.

Hyejin LeeCenter for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, Korea.
Wangyong ShinDepartment of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Korea.
Kyungdeok KimDepartment of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Korea.
Suho LeeCenter for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, Korea.
Eun-Jae LeeDepartment of Neurology, Asan Medical Center University of Ulsan, College of Medicine, Seoul, South Korea.
Jihye KimCenter for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, Korea.
Hanseul KweonDepartment of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Korea.
Eunee LeeCenter for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, Korea.
Haram ParkDepartment of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Korea.
Muwon KangDepartment of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Korea.
Esther YangDepartment of Anatomy, College of Medicine, Korea University, Seoul, Korea.
Hyun KimDepartment of Anatomy, College of Medicine, Korea University, Seoul, Korea.
Eunjoon KimCenter for Synaptic Brain Dysfunctions, Institute for Basic Science (IBS), Daejeon, Korea.ORCID 0000-0001-5518-6584
Korea Advanced Institute of Science and Technology · KRInstitute for Basic Science · KRKorea University · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Netrin-G ligand-3 (NGL-3) is a postsynaptic adhesion molecule known to directly interact with the excitatory postsynaptic scaffolding protein postsynaptic density-95 (PSD-95) and trans-synaptically with leukocyte common antigen-related (LAR) family receptor tyrosine phosphatases to regulate presynaptic differentiation. Although NGL-3 has been implicated in the regulation of excitatory synapse development by in vitro studies, whether it regulates synapse development or function, or any other features of brain development and function, is not known. Here, we report that mice lacking NGL-3 (Ngl3-/- mice) show markedly suppressed normal brain development and postnatal survival and growth. A change of the genetic background of mice from pure to hybrid minimized these developmental effects but modestly suppressed N-methyl-D-aspartate (NMDA) receptor (NMDAR)-mediated synaptic transmission in the hippocampus without affecting synapse development, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor (AMPAR)-mediated basal transmission, and presynaptic release. Intriguingly, long-term depression (LTD) was near-completely abolished in Ngl3-/- mice, and the Akt/glycogen synthase kinase 3β (GSK3β) signaling pathway, known to suppress LTD, was abnormally enhanced. In addition, pharmacological inhibition of Akt, but not activation of NMDARs, normalized the suppressed LTD in Ngl3-/- mice, suggesting that Akt hyperactivity suppresses LTD. Ngl3-/- mice displayed several behavioral abnormalities, including hyperactivity, anxiolytic-like behavior, impaired spatial memory, and enhanced seizure susceptibility. Among them, the hyperactivity was rapidly improved by pharmacological NMDAR activation. These results suggest that NGL-3 regulates brain development, Akt/GSK3β signaling, LTD, and locomotive and cognitive behaviors.

Indexed as

AnimalsBrainGlycogen Synthase Kinase 3 betaGPI-Linked ProteinsHippocampusLigandsLong-Term Synaptic DepressionMaleMiceMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsNetrinsNeuronal PlasticityNeuronsProto-Oncogene Proteins c-aktGlycogen Synthase Kinase 3 betaGPI-Linked ProteinsLigandsNerve Tissue ProteinsNetrinsNGL3 protein, mouseProto-Oncogene Proteins c-aktReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID31166939
PMCPMC6550391
OpenAlexW2948979641

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.