Evidence map›Paper›PMID 9822730›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

Specific agrin isoforms induce cAMP response element binding protein phosphorylation in hippocampal neurons.

R R Ji, C M Böse, C Lesuisse, D Qiu, J C Huang, Q Zhang, F Rupp

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. 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
2.1field-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

22 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Emerging roles for MAP kinases in agrin signaling.Communicative & integrative biology · 2011
    Article
  8. Agrin downregulation induced by nerve injury contributes to neuropathic pain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  9. Article
  10. Synapse loss in cortex of agrin-deficient mice after genetic rescue of perinatal death.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  11. Article
  12. MuSK expressed in the brain mediates cholinergic responses, synaptic plasticity, and memory formation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  13. Lipid rafts serve as a signaling platform for nicotinic acetylcholine receptor clustering.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Agrin differentially regulates the rates of axonal and dendritic elongation in cultured hippocampal neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  19. Agrin controls synaptic differentiation in hippocampal neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
    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

7 authors at 2 institutions in 1 country.

R R JiDepartment of Neuroscience, School of Medicine, The Johns Hopkins University, Baltimore, Maryland 21205, USA.
C M Böse
C Lesuisse
D Qiu
J C Huang
Q Zhang
F Rupp
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

THE ROLE OF AGRIN IN SYNAPTOGENESISR29MH051158 · NIMH · JOHNS HOPKINS UNIVERSITY · PI RUPP, FABIO P · 1994 to 1998
–
NIMH NIH HHS MH51158
6 · The paper itself

Abstract

The synaptic basal lamina protein agrin is essential for the formation of neuromuscular junctions. Agrin mediates the postsynaptic clustering of acetylcholine receptors and regulates transcription in muscles. Agrin expression is not restricted to motor neurons but can be demonstrated throughout the CNS. The functional significance of agrin expression in neurons other than motor neurons is unknown. To test whether agrin triggers responses in neurons that lead to the activation of transcription factors, we have analyzed phosphorylation of the transcriptional regulatory site serine 133 of the transcription factor CREB (cAMP response element binding protein) in primary hippocampal neurons. Our results indicate that the neuronal (Ag4,8), but not the non-neuronal (Ag0,0), isoform of agrin induces CREB phosphorylation in hippocampal neurons. The kinetics of agrin- and BDNF-induced CREB phosphorylation are similar: peak levels are reached in minutes and are strongly reduced 2 hr later. Neuronal responses to agrin require extracellular calcium, and, in contrast to tyrosine kinase inhibitors, the specific inhibition of protein kinase A (PKA) does not affect agrin-evoked CREB phosphorylation. Our results show that hippocampal neurons specifically respond to neuronal agrin in a Ca2+-dependent manner and via the activation of tyrosine kinases.

Indexed as

AgrinAnimalsBrain-Derived Neurotrophic FactorCalciumCells, CulturedColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinEnzyme InhibitorsHippocampusIsomerismNeuronsPhosphorylationProtein-Tyrosine KinasesRats8-((4-chlorophenyl)thio)cyclic-3',5'-AMPAgrinBrain-Derived Neurotrophic FactorCalciumColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinEnzyme InhibitorsProtein-Tyrosine KinasesThionucleotides

Identifiers

PMID9822730
PMCPMC6793297
OpenAlexW1770029100

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.