Evidence map›Paper›PMID 29348324›Full record

ArticleThe EMBO journal2018

PlexinD1 signaling controls morphological changes and migration termination in newborn neurons.

Masato Sawada, Nobuhiko Ohno, Mitsuyasu Kawaguchi, Shih-Hui Huang, Takao Hikita, Youmei Sakurai, Huy Bang Nguyen, Truc Quynh Thai, Yuri Ishido, Yutaka Yoshida and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  12. A Novel Loss-of-FunctionInternational journal of molecular sciences · 2022
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  16. Bio-protocol · 2020
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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

13 authors at 4 institutions in 2 countries.

Masato SawadaDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID 0000-0002-8694-8526
Nobuhiko OhnoDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki, Japan.
Mitsuyasu KawaguchiDepartment of Organic and Medicinal Chemistry, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.
Shih-Hui HuangDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Takao HikitaDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Youmei SakuraiDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Huy Bang NguyenDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki, Japan.
Truc Quynh ThaiDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki, Japan.
Yuri IshidoDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Yutaka YoshidaDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Hidehiko NakagawaDepartment of Organic and Medicinal Chemistry, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.
Akiyoshi UemuraDepartment of Retinal Vascular Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID 0000-0001-5574-5470
Kazunobu SawamotoDepartment of Developmental and Regenerative Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan sawamoto@med.nagoya-cu.ac.jp.ORCID 0000-0003-1984-5129
Nagoya City University · JPNational Institute for Physiological Sciences · JPCincinnati Children's Hospital Medical Center · USJichi Medical University · JP

Funding

Synapse elimination in the central nervous systemR01NS093002 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI YOSHIDA, YUTAKA · 2015 to 2024
$4.6M
NINDS NIH HHS R01 NS093002
6 · The paper itself

Abstract

Newborn neurons maintain a very simple, bipolar shape, while they migrate from their birthplace toward their destinations in the brain, where they differentiate into mature neurons with complex dendritic morphologies. Here, we report a mechanism by which the termination of neuronal migration is maintained in the postnatal olfactory bulb (OB). During neuronal deceleration in the OB, newborn neurons transiently extend a protrusion from the proximal part of their leading process in the resting phase, which we refer to as a filopodium-like lateral protrusion (FLP). The FLP formation is induced by PlexinD1 downregulation and local Rac1 activation, which coincide with microtubule reorganization and the pausing of somal translocation. The somal translocation of resting neurons is suppressed by microtubule polymerization within the FLP The timing of neuronal migration termination, controlled by Sema3E-PlexinD1-Rac1 signaling, influences the final positioning, dendritic patterns, and functions of the neurons in the OB These results suggest that PlexinD1 signaling controls FLP formation and the termination of neuronal migration through a precise control of microtubule dynamics.

Indexed as

Cell MovementNeurogenesisAnimalsAnimals, NewbornCells, CulturedCell Surface ExtensionsCytoskeletal ProteinsGlycoproteinsIntracellular Signaling Peptides and ProteinsMembrane GlycoproteinsMembrane ProteinsMiceMice, Inbred C57BLNerve Tissue ProteinsNeuronsNeuropeptidesCytoskeletal ProteinsGlycoproteinsIntracellular Signaling Peptides and ProteinsMembrane GlycoproteinsMembrane ProteinsNerve Tissue ProteinsNeuropeptidesPlxnd1 protein, mouserac1 GTP-Binding ProteinRac1 protein, mouseSema3e protein, mouseSemaphorinsmicrotubuleneuronal migrationolfactory bulbphotoactivationpostnatal neurogenesis

Identifiers

PMID29348324
PMCPMC5813262
OpenAlexW2784234813

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.