Evidence map›Paper›PMID 24719112›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

The serine/threonine kinase Ndr2 controls integrin trafficking and integrin-dependent neurite growth.

Kati Rehberg, Stefanie Kliche, Deniz A Madencioglu, Marlen Thiere, Bettina Müller, Bernhard Manuel Meineke, Christian Freund, Eike Budinger, Oliver Stork

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

39 citing papers in PubMed, 52 citations in OpenAlex.

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  7. The NDR family of kinases: essential regulators of aging.Frontiers in molecular neuroscience · 2024
    Review
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  18. Article
  19. Kinase Signaling in Dendritic Development and Disease.Frontiers in cellular neuroscience · 2021
    Review
  20. Review
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

9 authors at 5 institutions in 4 countries.

Kati RehbergDepartment of Genetics and Molecular Neurobiology, Institute of Biology, and Institute for Molecular and Clinical Immunology, Medical Faculty, Otto-von-Guericke University, 39120 Magdeburg, Germany, Department of Biochemistry, Institute for Chemistry and Biochemistry, Freie Universität Berlin, 14195 Berlin, Germany, Protein Engineering Group, Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany, Department of Auditory Learning and Speech, Leibniz-Institute for Neurobiology, 39118 Magdeburg, Germany, and Center for Behavioral Brain Sciences, 39106 Magdeburg, Germany.
Stefanie Kliche
Deniz A Madencioglu
Marlen Thiere
Bettina Müller
Bernhard Manuel Meineke
Christian Freund
Eike Budinger
Oliver Stork
Center for Behavioral Brain Sciences · DELeibniz Association · DEInstitute of Neurobiology · BGLaboratory of Molecular Genetics · PLOtto-von-Guericke University Magdeburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrins have been implicated in various processes of nervous system development, including proliferation, migration, and differentiation of neuronal cells. In this study, we show that the serine/threonine kinase Ndr2 controls integrin-dependent dendritic and axonal growth in mouse hippocampal neurons. We further demonstrate that Ndr2 is able to induce phosphorylation at the activity- and trafficking-relevant site Thr(788/789) of β1-integrin to stimulate the PKC- and CaMKII-dependent activation of β1-integrins, as well as their exocytosis. Accordingly, Ndr2 associates with integrin-positive early and recycling endosomes in primary hippocampal neurons and the surface expression of activated β1-integrins is reduced on dendrites of Ndr2-deficient neurons. The role of Ndr2 in dendritic differentiation is also evident in vivo, because Ndr2-null mutant mice show arbor-specific alterations of dendritic complexity in the hippocampus. This indicates a role of Ndr2 in the fine regulation of dendritic growth; in fact, treatment of primary neurons with Semaphorin 3A rescues Ndr2 knock-down-induced dendritic growth deficits but fails to enhance growth beyond control level. Correspondingly, Ndr2-null mutant mice show a Semaphorin 3A(-/-)-like phenotype of premature dendritic branching in the hippocampus. The results of this study show that Ndr2-mediated integrin trafficking and activation are crucial for neurite growth and guidance signals during neuronal development.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell Growth ProcessesCells, CulturedEndosomesGene DeletionHEK293 CellsHippocampusHumansIntegrin beta1MiceMice, Inbred C57BLNeuritesNIH 3T3 CellsPC12 CellsPhosphorylationAdaptor Proteins, Signal TransducingIntegrin beta1Ndr2 protein, mouseProteinsSemaphorin-3Adendritic and axonal growthdendritic branchingintegrin activationintegrin traffickingmouseserine/threonine kinase Ndr2

Identifiers

PMID24719112
PMCPMC6609001
OpenAlexW2093944536

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.