Evidence map›Paper›PMID 23066017›Full record

ArticleThe Journal of biological chemistry2012

Neuritin activates insulin receptor pathway to up-regulate Kv4.2-mediated transient outward K+ current in rat cerebellar granule neurons.

Jin-Jing Yao, Xiao-Fei Gao, Chi-Wing Chow, Xiao-Qin Zhan, Chang-Long Hu, Yan-Ai Mei

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  12. International journal of molecular sciences · 2022
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  19. Cholecystokinin type B receptor-mediated inhibition of A-type KCell communication and signaling : CCS · 2019
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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

6 authors at 3 institutions in 2 countries.

Jin-Jing YaoInstitutes of Brain Science, School of Life Sciences and State Key Laboratory of Medical Neurobiology, Fudan University, Shanghai 200433, China.
Xiao-Fei Gao
Chi-Wing Chow
Xiao-Qin Zhan
Chang-Long Hu
Yan-Ai Mei
Fudan University · CNState Key Laboratory of Medical NeurobiologyAlbert Einstein College of Medicine · US

Funding

Molecular Signaling in AdipocytesR01DK090481 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHOW, CHI-WING · 2011 to 2014
$1.5M
NIDDK NIH HHS R01 DK090481
6 · The paper itself

Abstract

Neuritin is a new neurotrophic factor discovered in a screen to identify genes involved in activity-dependent synaptic plasticity. Neuritin also plays multiple roles in the process of neural development and synaptic plasticity. The receptors for binding neuritin and its downstream signaling effectors, however, remain unclear. Here, we report that neuritin specifically increases the densities of transient outward K(+) currents (I(A)) in rat cerebellar granule neurons (CGNs) in a time- and concentration-dependent manner. Neuritin-induced amplification of I(A) is mediated by increased mRNA and protein expression of Kv4.2, the main α-subunit of I(A). Exposure of CGNs to neuritin markedly induces phosphorylation of ERK (pERK), Akt (pAkt), and mammalian target of rapamycin (pmTOR). Neuritin-induced I(A) and increased expression of Kv4.2 are attenuated by ERK, Akt, or mTOR inhibitors. Unexpectedly, pharmacological blockade of insulin receptor, but not the insulin-like growth factor 1 receptor, abrogates the effect of neuritin on I(A) amplification and Kv4.2 induction. Indeed, neuritin activates downstream signaling effectors of the insulin receptor in CGNs and HeLa. Our data reveal, for the first time, an unanticipated role of the insulin receptor in previously unrecognized neuritin-mediated signaling.

Indexed as

Gene Expression RegulationAnimalsCerebellumDose-Response Relationship, DrugExtracellular Signal-Regulated MAP KinasesGPI-Linked ProteinsHeLa CellsHumansKineticsModels, BiologicalNeuronsNeuropeptidesPatch-Clamp TechniquesRatsReceptor, InsulinShal Potassium ChannelsExtracellular Signal-Regulated MAP KinasesGPI-Linked ProteinsNeuropeptidesNrn1 protein, ratReceptor, InsulinShal Potassium Channels

Identifiers

PMID23066017
PMCPMC3510849
OpenAlexW2004589561

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.