Evidence map›Paper›PMID 31685650›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Dynamic Changes in Ultrastructure of the Primary Cilium in Migrating Neuroblasts in the Postnatal Brain.

Mami Matsumoto, Masato Sawada, Diego García-González, Vicente Herranz-Pérez, Takashi Ogino, Huy Bang Nguyen, Truc Quynh Thai, Keishi Narita, Natsuko Kumamoto, Shinya Ugawa and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

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  14. Neuronal guidance behaviours: the primary cilium perspective.Frontiers in cell and developmental biology · 2025
    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

18 authors at 10 institutions in 5 countries.

Mami MatsumotoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0003-1406-5916
Masato SawadaDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.ORCID 0000-0002-8694-8526
Diego García-GonzálezDepartment of Clinical Neurobiology, Medical Faculty of Heidelberg University and German Cancer Research Center, 69120 Heidelberg, Germany.ORCID 0000-0002-2500-0248
Vicente Herranz-PérezLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, CIBERNED, 46980, Valencia, Spain.ORCID 0000-0002-1969-1214
Takashi OginoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Huy Bang NguyenDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki 444-8787, Japan.ORCID 0000-0002-7823-067X
Truc Quynh ThaiDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki 444-8787, Japan.
Keishi NaritaDepartment of Anatomy and Cell Biology, Faculty of Medicine, University of Yamanashi, Chuo 409-3898, Japan.
Natsuko KumamotoDepartment of Anatomy and Neuroscience, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Shinya UgawaDepartment of Anatomy and Neuroscience, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Yumiko SaitoGraduate School of Integrated Sciences for Life, Hiroshima University, Hiroshima 739-8521, Japan.
Sen TakedaDepartment of Anatomy and Cell Biology, Faculty of Medicine, University of Yamanashi, Chuo 409-3898, Japan.
Naoko KanekoDepartment of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Konstantin KhodosevichBiotech Research & Innovation Centre, University of Copenhagen, 2200 Copenhagen, Denmark.
Hannah MonyerDepartment of Clinical Neurobiology, Medical Faculty of Heidelberg University and German Cancer Research Center, 69120 Heidelberg, Germany.
José Manuel García-VerdugoLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, CIBERNED, 46980, Valencia, Spain.
Nobuhiko OhnoDivision of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki 444-8787, 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 · JPUniversity of Copenhagen · DKUniversity of Yamanashi · JPGerman Cancer Research Center · DEHiroshima University · JPJichi Medical University · JPPham Ngoc Thach University of Medicine · VNUniversitat de València · ESUniversitat Jaume I · ESUniversity of Medicine and Pharmacy at Ho Chi Minh City · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New neurons, referred to as neuroblasts, are continuously generated in the ventricular-subventricular zone of the brain throughout an animal's life. These neuroblasts are characterized by their unique potential for proliferation, formation of chain-like cell aggregates, and long-distance and high-speed migration through the rostral migratory stream (RMS) toward the olfactory bulb (OB), where they decelerate and differentiate into mature interneurons. The dynamic changes of ultrastructural features in postnatal-born neuroblasts during migration are not yet fully understood. Here we report the presence of a primary cilium, and its ultrastructural morphology and spatiotemporal dynamics, in migrating neuroblasts in the postnatal RMS and OB. The primary cilium was observed in migrating neuroblasts in the postnatal RMS and OB in male and female mice and zebrafish, and a male rhesus monkey. Inhibition of intraflagellar transport molecules in migrating neuroblasts impaired their ciliogenesis and rostral migration toward the OB. Serial section transmission electron microscopy revealed that each migrating neuroblast possesses either a pair of centrioles or a basal body with an immature or mature primary cilium. Using immunohistochemistry, live imaging, and serial block-face scanning electron microscopy, we demonstrate that the localization and orientation of the primary cilium are altered depending on the mitotic state, saltatory migration, and deceleration of neuroblasts. Together, our results highlight a close mutual relationship between spatiotemporal regulation of the primary cilium and efficient chain migration of neuroblasts in the postnatal brain.

Indexed as

AnimalsCell MovementCiliaFemaleLateral VentriclesMacaca mulattaMaleMiceNeural Stem CellsNeuronsOlfactory BulbZebrafishelectron microscopylive imagingneuronal migrationolfactory bulbprimary ciliumrostral migratory stream

Identifiers

PMID31685650
PMCPMC6978947
OpenAlexW2987143724

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.