Evidence map›Paper›PMID 18458158›Full record

ArticleThe Journal of cell biology2008

Presynaptic type III neuregulin1-ErbB signaling targets {alpha}7 nicotinic acetylcholine receptors to axons.

Melissa L Hancock, Sarah E Canetta, Lorna W Role, David A Talmage

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Structural Similarities between Neuregulin 1-3 Isoforms Determine Their Subcellular Distribution and Signaling Mode in Central Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Type III neuregulin 1 is required for multiple forms of excitatory synaptic plasticity of mouse cortico-amygdala circuits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  17. Article
  18. Article
  19. Disrupted activity in the hippocampal-accumbens circuit of type III neuregulin 1 mutant mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Melissa L HancockIntegrated Program in Cellular, Molecular and Biophysical Studies, Columbia University, New York, NY 10032, USA.
Sarah E Canetta
Lorna W Role
David A Talmage
Center for Neurosciences · USColumbia University · US

Funding

Hormones: Molecular Mechanism of Action and FunctionsT32DK007328 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KOUSTENI, STAVROULA · 1986 to 2025
$7.8M
EXPRESSION OF NEURONAL NICOTINIC ACETYLOCHOLINE RECEPTORR01NS029071 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI ROLE, LORNA W · 1991 to 2009
$3.6M
In vivo studies of Neuregulin 1 in addiction pathwaysR21DA019941 · NIDA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI ROLE, LORNA W · 2005 to 2006
$261k
NIDA NIH HHS DA019941NIDA NIH HHS R21 DA019941NIDDK NIH HHS DK07328NIDDK NIH HHS T32 DK007328NINDS NIH HHS NS29071NINDS NIH HHS R01 NS029071
6 · The paper itself

Abstract

Type III Neuregulin1 (Nrg1) isoforms are membrane-tethered proteins capable of participating in bidirectional juxtacrine signaling. Neuronal nicotinic acetylcholine receptors (nAChRs), which can modulate the release of a rich array of neurotransmitters, are differentially targeted to presynaptic sites. We demonstrate that Type III Nrg1 back signaling regulates the surface expression of alpha7 nAChRs along axons of sensory neurons. Stimulation of Type III Nrg1 back signaling induces an increase in axonal surface alpha7 nAChRs, which results from a redistribution of preexisting intracellular pools of alpha7 rather than from increased protein synthesis. We also demonstrate that Type III Nrg1 back signaling activates a phosphatidylinositol 3-kinase signaling pathway and that activation of this pathway is required for the insertion of preexisting alpha7 nAChRs into the axonal plasma membrane. These findings, in conjunction with prior results establishing that Type III Nrg1 back signaling controls gene transcription, demonstrate that Type III Nrg1 back signaling can regulate both short-and long-term changes in neuronal function.

Indexed as

alpha7 Nicotinic Acetylcholine ReceptorAnimalsAxonsCells, CulturedEmbryo, MammalianEndocytosisGanglia, SpinalGene Expression RegulationMiceMice, KnockoutNeuregulin-1Oncogene Proteins v-erbBPhosphatidylinositol 3-KinasesProtein IsoformsProto-Oncogene Proteins c-aktReceptors, Nicotinicalpha7 Nicotinic Acetylcholine ReceptorChrna7 protein, mouseNeuregulin-1Oncogene Proteins v-erbBPhosphatidylinositol 3-KinasesProtein IsoformsProto-Oncogene Proteins c-aktReceptors, NicotinicReceptors, Presynaptic

Identifiers

PMID18458158
PMCPMC2364689
OpenAlexW2120892416

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.