Evidence map›Paper›PMID 21554942›Full record

ArticleHearing research2011

Activity of all JNK isoforms contributes to neurite growth in spiral ganglion neurons.

Patrick J Atkinson, Chang-Hyun Cho, Marlan R Hansen, Steven H Green

Open access · greenAbstract read
In one paragraph

Article in Hearing research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.8field-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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. MEKK4 Signaling Regulates Sensory Cell Development and Function in the Mouse Inner Ear.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  11. On the Horizon: Cochlear Implant Technology.Otolaryngologic clinics of North America · 2015
    Review
  12. Article
  13. The role of brain-derived neurotrophic factor (BDNF) in the development of neurogenic detrusor overactivity (NDO).The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 2 institutions in 2 countries.

Patrick J AtkinsonDepartment of Biology, University of Iowa, 143 Biology Building, Iowa City, IA 52242, USA.
Chang-Hyun Cho
Marlan R Hansen
Steven H Green
University of Iowa · USGachon University · KR

Funding

Stimuli promoting the survival of spiral ganglion neuronsR01DC002961 · NIDCD · UNIVERSITY OF IOWA · PI GREEN, STEVEN H · 1996 to 2011
$3.6M
Tissue Culture CoreP30DC010362 · NIDCD · UNIVERSITY OF IOWA · PI DAILEY, MICHAEL E, FRITZSCH, BERND · 2010 to 2014
$2.0M
Contribution of c-Jun N-terminal kinase activity to vestibular schwannoma growthR01DC009801 · NIDCD · UNIVERSITY OF IOWA · PI HANSEN, MARLAN R · 2009 to 2013
$1.8M
Reinnervation of inner hair cells following excitotoxic traumaR01DC009405 · NIDCD · UNIVERSITY OF IOWA · PI GREEN, STEVEN H · 2011 to 2015
$1.6M
Regulation of auditory neuron neurite growth by activityK08DC006211 · NIDCD · UNIVERSITY OF IOWA · PI HANSEN, MARLAN R · 2004 to 2008
$957k
NIDCD NIH HHS K08 DC006211NIDCD NIH HHS KO8 DC006211-01A1NIDCD NIH HHS P30 DC010362NIDCD NIH HHS R01 DC002961NIDCD NIH HHS R01 DC009405NIDCD NIH HHS R01 DC009801NIDCD NIH HHS R01 DC02961
6 · The paper itself

Abstract

Jun N-terminal kinase (JNK) is a multifunctional protein kinase crucial for neuronal apoptosis as well as neurite growth. We have previously shown that JNK activity is correlated with spiral ganglion neuron (SGN) apoptosis following hair cell loss in rats (Alam et al., 2007) implying that JNK inhibition may have therapeutic potential to protect SGNs in deaf individuals. Here we investigated the role of JNK in neurite outgrowth from cultured neonatal rat and mouse SGNs. We show that JNK is required for initial growth of neurites and for continued extension of already established neurites. The effect of JNK inhibition on neurite growth is rapid and is also rapidly reversible after washout of the inhibitor. Using phosphoJNK immunoreactivity as an indicator, we show that JNK is activated in growth cones within 30 min after transfer to medium lacking neurotrophic stimuli (5 K medium) but activation in the nucleus and soma requires hours. By transfecting epitope-tagged JNK1, JNK2, or JNK3 isoforms into SGNs, we found that all are present in the nucleus and cytoplasm and that there is no preferential redistribution to the nucleus after transfer to 5 K medium. Cotransfection of dominant-negative (dn) JNK1 and JNK2 into SGNs reduced neurite growth, although transfection of dnJNK1 or dnJNK2 alone had no significant effect. SGNs cultured from JNK3(-/-) mice showed reduced neurite growth that was further reduced by transfection of dnJNK1 and dnJNK2. This indicates that all three JNK isoforms promote SGN neurite growth although there may be functional redundancy between JNK1 and JNK2.

Indexed as

MAP Kinase Signaling SystemAnimalsCells, CulturedEnzyme ActivationKineticsMAP Kinase Kinase KinasesMiceMice, KnockoutMitogen-Activated Protein Kinase 10Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein Kinase 9NeuritesNeuronsPhosphorylationRatsSpiral GanglionMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase 10Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein Kinase 9

Identifiers

PMID21554942
PMCPMC3152600
OpenAlexW1998400942

What OpenQuestion holds

Textmetadata
LicenceTDM
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.