Evidence map›Paper›PMID 38461182›Full record

ArticleNature communications2024

Identification of the growth cone as a probe and driver of neuronal migration in the injured brain.

Chikako Nakajima, Masato Sawada, Erika Umeda, Yuma Takagi, Norihiko Nakashima, Kazuya Kuboyama, Naoko Kaneko, Satoaki Yamamoto, Haruno Nakamura, Naoki Shimada and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  3. Functionalized Biomimetic Scaffolds for Human-Derived Auditory Neural Circuit Construction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  8. Neuronal Axon Generation/Regeneration Regulated by Sulfated Glycans.Advances in experimental medicine and biology · 2026
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Neuronal guidance behaviours: the primary cilium perspective.Frontiers in cell and developmental biology · 2025
    Review
  14. Article
  15. Article
  16. 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

28 authors at 10 institutions in 4 countries.

Chikako Nakajima *Department of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.ORCID 0000-0003-3071-8585
Masato Sawada *Department of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Erika UmedaDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Yuma TakagiDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Norihiko NakashimaDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Kazuya KuboyamaDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Naoko KanekoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Satoaki YamamotoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Haruno NakamuraDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Naoki ShimadaResearch and Development Center, The Japan Wool Textile Co., Ltd., Kobe, 675-0053, Japan.
Koichiro NakamuraMedical Device Department, Nikke Medical Co., Ltd., Osaka, 541-0048, Japan.
Kumiko MatsunoResearch and Development Center, The Japan Wool Textile Co., Ltd., Kobe, 675-0053, Japan.
Shoji UesugiMedical Device Department, Nikke Medical Co., Ltd., Osaka, 541-0048, Japan.
Nynke A VepřekDepartment of Chemistry, New York University, New York, NY, 10003, USA.ORCID 0000-0001-7301-265X
Florian KüllmerInstitute for Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Jena, 07743, Germany.ORCID 0000-0002-0671-1546
Veselin NasufovićInstitute for Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Jena, 07743, Germany.ORCID 0000-0001-6812-637X
Hironobu UchiyamaToray Research Center, Inc., Otsu, 520-8567, Japan.
Masaru NakadaToray Research Center, Inc., Otsu, 520-8567, Japan.
Yuji OtsukaToray Research Center, Inc., Otsu, 520-8567, Japan.
Yasuyuki ItoDepartment of Neurochemistry and Molecular Cell Biology, School of Medicine and Graduate School of Medical/Dental Sciences, Niigata University, Niigata, 951-8510, Japan.
Vicente Herranz-PérezLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, CIBERNED, Valencia, 46980, Spain.ORCID 0000-0002-1969-1214
José Manuel García-VerdugoLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, CIBERNED, Valencia, 46980, Spain.ORCID 0000-0001-9872-6499
Nobuhiko OhnoDepartment of Anatomy, Division of Histology and Cell Biology, Jichi Medical University, School of Medicine, Shimotsuke, 329-0498, Japan.
Hans-Dieter ArndtInstitute for Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Jena, 07743, Germany.ORCID 0000-0002-0792-1422
Dirk TraunerDepartment of Chemistry, New York University, New York, NY, 10003, USA.
Yasuhiko TabataLaboratory of Biomaterials, Department of Regeneration Science and Engineering, Institute for Life and Medical Sciences (LiMe), Kyoto University, Kyoto, 606-8507, Japan.ORCID 0000-0001-8974-277X
Michihiro IgarashiDepartment of Neurochemistry and Molecular Cell Biology, School of Medicine and Graduate School of Medical/Dental Sciences, Niigata University, Niigata, 951-8510, Japan.
Kazunobu SawamotoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan. sawamoto@med.nagoya-cu.ac.jp.ORCID 0000-0003-1984-5129
Nagoya City University · JPFriedrich Schiller University Jena · DEToray Industries, Inc. (Japan) · JPKyoto University · JPNiigata University · JPUniversitat de València · ESDoshisha University · JPJichi Medical University · JPNew York University · USTranslational Therapeutics (United States) · US

Funding

Japan Agency for Medical Research and Development (AMED) 23gm1210007, 21bm0704033h0003
6 · The paper itself

Abstract

Axonal growth cones mediate axonal guidance and growth regulation. We show that migrating neurons in mice possess a growth cone at the tip of their leading process, similar to that of axons, in terms of the cytoskeletal dynamics and functional responsivity through protein tyrosine phosphatase receptor type sigma (PTPσ). Migrating-neuron growth cones respond to chondroitin sulfate (CS) through PTPσ and collapse, which leads to inhibition of neuronal migration. In the presence of CS, the growth cones can revert to their extended morphology when their leading filopodia interact with heparan sulfate (HS), thus re-enabling neuronal migration. Implantation of an HS-containing biomaterial in the CS-rich injured cortex promotes the extension of the growth cone and improve the migration and regeneration of neurons, thereby enabling functional recovery. Thus, the growth cone of migrating neurons is responsive to extracellular environments and acts as a primary regulator of neuronal migration.

Indexed as

Growth ConesReceptor-Like Protein Tyrosine Phosphatases, Class 2AnimalsAxonsBrainCells, CulturedChondroitin SulfatesMiceNeurogenesisChondroitin SulfatesReceptor-Like Protein Tyrosine Phosphatases, Class 2

Identifiers

PMID38461182
PMCPMC10924819
OpenAlexW4392614967

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.