Evidence map›Paper›PMID 25224226›Full record

ArticleDevelopmental biology2014

MACF1 regulates the migration of pyramidal neurons via microtubule dynamics and GSK-3 signaling.

Minhan Ka, Eui-Man Jung, Ulrich Mueller, Woo-Yang Kim

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

62 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. A clinical and genotype-phenotype analysis of MACF1 variants.American journal of human genetics · 2025
    Article
  3. Article
  4. Optogenetic and Endogenous Modulation of CaInternational journal of molecular sciences · 2025
    Review
  5. Domain specific phenotypic expansion associated with variants inmedRxiv : the preprint server for health sciences · 2025
    Article
  6. Identification ofJournal of medical genetics · 2025
    Article
  7. A Multifaceted Giant Protein Microtubule-Actin Cross-Linking Factor 1.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. TheMolecular biology of the cell · 2022
    Article
  18. Article
  19. Review
  20. Article

2 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Minhan KaDevelopmental Neuroscience, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE 68198, United States.
Eui-Man JungDevelopmental Neuroscience, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE 68198, United States.
Ulrich MuellerDorris Neuroscience Center and Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, United States.
Woo-Yang KimDevelopmental Neuroscience, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE 68198, United States. Electronic address: wooyang.kim@unmc.edu.
Nebraska Medical Center · USScripps Research Institute · US

Funding

UNMC Histology/Imaging and Creighton University Imaging Core FacilityP30GM110768 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SMITH, SHELLEY D · 2014 to 2018
$5.1M
Cell Adhesion Molecules in CNS DevelopmentR01NS046456 · NINDS · SCRIPPS RESEARCH INSTITUTE, THE · PI MUELLER, ULRICH · 2004 to 2013
$4.4M
The Molecular Biology of Neurosurgery SystemsP20GM103471 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SMITH, SHELLEY D · 2012 to 2013
$4.1M
NIGMS NIH HHS P20 GM103471NIGMS NIH HHS P20GM103471NIGMS NIH HHS P30 GM110768NINDS NIH HHS R01 NS046456
6 · The paper itself

Abstract

Neuronal migration and subsequent differentiation play critical roles for establishing functional neural circuitry in the developing brain. However, the molecular mechanisms that regulate these processes are poorly understood. Here, we show that microtubule actin crosslinking factor 1 (MACF1) determines neuronal positioning by regulating microtubule dynamics and mediating GSK-3 signaling during brain development. First, using MACF1 floxed allele mice and in utero gene manipulation, we find that MACF1 deletion suppresses migration of cortical pyramidal neurons and results in aberrant neuronal positioning in the developing brain. The cell autonomous deficit in migration is associated with abnormal dynamics of leading processes and centrosomes. Furthermore, microtubule stability is severely damaged in neurons lacking MACF1, resulting in abnormal microtubule dynamics. Finally, MACF1 interacts with and mediates GSK-3 signaling in developing neurons. Our findings establish a cellular mechanism underlying neuronal migration and provide insights into the regulation of cytoskeleton dynamics in developing neurons.

Indexed as

Cell MovementSignal TransductionAnimalsBlotting, WesternBrainCentrosomeCytoskeletonGlycogen Synthase Kinase 3Green Fluorescent ProteinsIsoenzymesKineticsMice, KnockoutMicrofilament ProteinsMicroscopy, ConfocalMicrotubulesModels, BiologicalGlycogen Synthase Kinase 3Green Fluorescent ProteinsIsoenzymesMacf1 protein, mouseMicrofilament ProteinsCytoskeletonGSK-3MACF1MicrotubuleNeuronal migration

Identifiers

PMID25224226
PMCPMC4190130
OpenAlexW2171483753

What OpenQuestion holds

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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.