Evidence map›Paper›PMID 31123102›Full record

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

Sensory Axon Growth Requires Spatiotemporal Integration of CaSR and TrkB Signaling.

Ronja Markworth, Youri Adolfs, Vivian Dambeck, Lars M Steinbeck, Muriel Lizé, R Jeroen Pasterkamp, Mathias Bähr, Camin Dean, Katja Burk

Open access · hybridAbstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Silencing the enhancer of zeste homologue 2,Neural regeneration research · 2022
    Article
  5. Review
  6. 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 4 institutions in 2 countries.

Ronja MarkworthDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0003-1893-4752
Youri AdolfsDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht University, 3584 CG Utrecht, The Netherlands.
Vivian DambeckDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Lars M SteinbeckCenter for Biostructural Imaging of Neurodegeneration, 37075 Göttingen, Germany, and.ORCID 0000-0002-9870-6735
Muriel LizéDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-4954-3503
R Jeroen PasterkampDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht University, 3584 CG Utrecht, The Netherlands.ORCID 0000-0003-1631-6440
Mathias BährDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Camin DeanEuropean Neuroscience Institute, 37077 Göttingen, Germany.ORCID 0000-0002-7969-5014
Katja BurkDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany, kburk@gwdg.de.ORCID 0000-0001-6083-4152
German Center for Neurodegenerative Diseases · DEUniversitätsmedizin Göttingen · DEUtrecht University · NLEuropean Neuroscience Institute Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neural circuit development involves the coordinated growth and guidance of axons. During this process, axons encounter many different cues, but how these cues are integrated and translated into growth is poorly understood. In this study, we report that receptor signaling does not follow a linear path but changes dependent on developmental stage and coreceptors involved. Using developing chicken embryos of both sexes, our data show that calcium-sensing receptor (CaSR), a G-protein-coupled receptor important for regulating calcium homeostasis, regulates neurite growth in two distinct ways. First, when signaling in isolation, CaSR promotes growth through the PI3-kinase-Akt pathway. At later developmental stages, CaSR enhances tropomyosin receptor kinase B (TrkB)/BDNF-mediated neurite growth. This enhancement is facilitated through a switch in the signaling cascade downstream of CaSR (i.e., from the PI3-kinase-Akt pathway to activation of GSK3α Tyr279). TrkB and CaSR colocalize within late endosomes, cotraffic and coactivate GSK3, which serves as a shared signaling node for both receptors. Our study provides evidence that two unrelated receptors can integrate their individual signaling cascades toward a nonadditive effect and thus control neurite growth during development.

Indexed as

AnimalsAxonsCell EnlargementCells, CulturedChick EmbryoFemaleHEK293 CellsHumansMaleMembrane GlycoproteinsMiceMice, Inbred C57BLNodose GanglionProtein-Tyrosine KinasesReceptors, Calcium-SensingReceptor, trkBCASR protein, mouseMembrane GlycoproteinsNtrk2 protein, mouseProtein-Tyrosine KinasesReceptors, Calcium-SensingReceptor, trkBCaSRcosignalingGSK3neurite growthsignal integrationTrkB

Identifiers

PMID31123102
PMCPMC6650981
OpenAlexW2946172104

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.