Evidence map›Paper›PMID 15788763›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Distinct roles of calcineurin-nuclear factor of activated T-cells and protein kinase A-cAMP response element-binding protein signaling in presynaptic differentiation.

Tomoyuki Yoshida, Masayoshi Mishina

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Axonal CB1 Receptors Mediate Inhibitory Bouton Formation via cAMP Increase and PKA.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
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  11. BDNF and glucocorticoids regulate corticotrophin-releasing hormone (CRH) homeostasis in the hypothalamus.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  14. Mitochondrial Ca2+ cycling facilitates activation of the transcription factor NFAT in sensory neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  15. Article
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  17. NFAT signaling in neural development and axon growth.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2008
    Review
  18. Article
  19. Myosin Va controls oligodendrocyte morphogenesis and myelination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  20. Article
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

2 authors at 1 institution in 1 country.

Tomoyuki YoshidaDepartment of Molecular Neurobiology and Pharmacology, Graduate School of Medicine, University of Tokyo, and Solution-Oriented Research for Science and Technology, Japan Science and Technology Corporation, Tokyo 113-0033, Japan.
Masayoshi Mishina
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synaptic vesicle accumulation and morphological changes are characteristic features of axon terminal differentiation during synaptogenesis. To investigate the regulatory mechanism that orchestrates synaptic molecules to form mature presynaptic terminals, we visualized a single axon terminal of zebrafish olfactory sensory neurons in vivo and examined the effects of the neuron-specific gene manipulations on the axon terminal differentiation. Synaptic vesicles visualized with vesicle-associated membrane protein 2 (VAMP2)-enhanced green fluorescent protein (EGFP) fusion protein gradually accumulated in axon terminals, whereas the axon terminals visualized with GAP43 fused with EGFP remodeled from complex shapes with filopodia to simple shapes without filopodia from 50 h postfertilization (hpf) to 84 hpf. Expression of dominant-negative protein kinase A (PKA) or cAMP response element-binding protein (CREB) suppressed the VAMP2-EGFP punctum formation in axon terminals during synaptogenesis. Consistently, constitutively active PKA or CREB stimulated VAMP2-EGFP puncta formation. On the other hand, cyclosporine A treatment or suppression of nuclear factor of activated T cells (NFAT) activation prevented the axon terminal remodeling from complex to simple shapes during synaptogenesis. Consistently, expression of constitutively active calcineurin accelerated the axon terminal remodeling. These results suggest that calcineurin-NFAT signaling regulates axon terminal remodeling, and PKA-CREB signaling controls synaptic vesicle accumulation.

Indexed as

Age FactorsAnimalsAnimals, Genetically ModifiedCalcineurinCell DifferentiationCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinCyclosporineDiagnostic ImagingDNA-Binding ProteinsEmbryo, NonmammalianEnzyme InhibitorsGAP-43 ProteinGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsImmunohistochemistryCalcineurinCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinCyclosporineDNA-Binding ProteinsEnzyme InhibitorsGAP-43 ProteinGreen Fluorescent ProteinsNFATC Transcription FactorsRNA, MessengerT-Box Domain Proteinstbr1b protein, zebrafishVesicle-Associated Membrane Protein 2Zebrafish Proteins

Identifiers

PMID15788763
PMCPMC6725083
OpenAlexW2056815050

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.