Evidence map›Paper›PMID 31650708›Full record

ArticleEMBO reports2019

Radial somatic F-actin organization affects growth cone dynamics during early neuronal development.

Durga Praveen Meka, Robin Scharrenberg, Bing Zhao, Oliver Kobler, Theresa König, Irina Schaefer, Birgit Schwanke, Sergei Klykov, Melanie Richter, Dennis Eggert and 5 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Moonlighting at the Poles: Non-Canonical Functions of Centrosomes.Frontiers in cell and developmental biology · 2022
    Review
  6. Review
  7. Article
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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

15 authors at 4 institutions in 2 countries.

Durga Praveen MekaRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-1058-9827
Robin ScharrenbergRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-7825-894X
Bing ZhaoRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Oliver KoblerCombinatorial Neuroimaging Core Facility (CNI), Leibniz Institute for Neurobiology, Magdeburg, Germany.ORCID 0000-0001-7173-9919
Theresa KönigRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Irina SchaeferRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Birgit SchwankeRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sergei KlykovEmmy-Noether Group "Neuronal Protein Transport", Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Melanie RichterRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Dennis EggertMax Planck Institute for the Structure and Dynamics of Matter, Hamburg, Germany.
Sabine WindhorstDepartment of Biochemistry and Signal Transduction, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Carlos G DottiCentro de Biología Molecular "Severo Ochoa", CSIC-UAM, Madrid, Spain.ORCID 0000-0003-4052-1719
Michael R KreutzRG Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany.ORCID 0000-0003-0575-6950
Marina MikhaylovaEmmy-Noether Group "Neuronal Protein Transport", Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-7646-1346
Froylan Calderon de AndaRG Neuronal Development, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-2743-7774
Universität Hamburg · DECentro de Biología Molecular Severo Ochoa · ESLeibniz Institute for Neurobiology · DELeibniz Institute of Virology (LIV) · DE

Funding

BMBF EnergiBundesministerium für Bildung und Forschung, BMBF (ERA-NET Neuron) 01EW1410Bundesministerium für Bildung und Forschung, BMBF (ERA-NET Neuron) 01EW1910Bundesministerium für Bildung und Forschung, BMBF (JPND) 01ED1806Deutsche Forschungsgemeinschaft (DFG) CA 1495/1-1Deutsche Forschungsgemeinschaft (DFG) CA 1495/4-1Deutsche Forschungsgemeinschaft (DFG) FOR 2419Deutsche Forschungsgemeinschaft (DFG) SCHE 132/18-1Deutsche Forschungsgemeinschaft (DFG Emmy-Noether Programm) MI 1923/2-1Deutsche Forschungsgemeinschaft (DFG Emmy-Noether Programm) Ml 1923/1-1JPND STADLeibniz Foundation, Deutsche Forschungsgemeinschaft Kr1879 5-1, 6-1Leibniz Foundation, Deutsche Forschungsgemeinschaft SFB 779 TPB8University Medical Center Hamburg-Eppendorf (UKE)
6 · The paper itself

Abstract

The centrosome is thought to be the major neuronal microtubule-organizing center (MTOC) in early neuronal development, producing microtubules with a radial organization. In addition, albeit in vitro, recent work showed that isolated centrosomes could serve as an actin-organizing center, raising the possibility that neuronal development may, in addition, require a centrosome-based actin radial organization. Here, we report, using super-resolution microscopy and live-cell imaging of cultured rodent neurons, F-actin organization around the centrosome with dynamic F-actin aster-like structures with F-actin fibers extending and retracting actively. Photoactivation/photoconversion experiments and molecular manipulations of F-actin stability reveal a robust flux of somatic F-actin toward the cell periphery. Finally, we show that somatic F-actin intermingles with centrosomal PCM-1 (pericentriolar material 1 protein) satellites. Knockdown of PCM-1 and disruption of centrosomal activity not only affect F-actin dynamics near the centrosome but also in distal growth cones. Collectively, the data show a radial F-actin organization during early neuronal development, which might be a cellular mechanism for providing peripheral regions with a fast and continuous source of actin polymers, hence sustaining initial neuronal development.

Indexed as

NeurogenesisActinsAnimalsCell Cycle ProteinsCells, CulturedCentrosomeGrowth ConesHippocampusMiceMice, Inbred C57BLMicrotubulesRatsActinsCell Cycle ProteinsPcm1 protein, mouseactincentrosomemicrotubulesneuronal developmentPCM-1

Identifiers

PMID31650708
PMCPMC6893363
OpenAlexW2981595470

What Socratic holds

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LicenceCC BY
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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 Socratic graph.