Evidence map›Paper›PMID 21557511›Full record

ArticleDevelopmental neurobiology2011

Modulation of neurite outgrowth by activation of calcium-permeable kainate receptors expressed by rat nociceptive-like dorsal root ganglion neurons.

Donald J Joseph, Damian J Williams, Amy B MacDermott

Abstract read
In one paragraph

Article in Developmental neurobiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Neto2 Assembles with Kainate Receptors in DRG Neurons during Development and Modulates Neurite Outgrowth in Adult Sensory Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  9. Article
  10. Article
  11. CRMP2 tethers kainate receptor activity to cytoskeleton dynamics during neuronal maturation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  12. Article
  13. Review
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

3 authors at 1 institution in 1 country.

Donald J JosephDepartment of Neuroscience, Program in Neurobiology and Behavior, Columbia University, New York, New York 10032, USA.
Damian J Williams
Amy B MacDermott
Columbia University · US

Funding

Synaptic regulation of dorsal horn projection neuronsR01NS029797 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MACDERMOTT, AMY B · 1992 to 2010
$3.4M
Transmitter release from peripheral sensory neuronsR01NS053575 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MACDERMOTT, AMY B · 2006 to 2010
$1.7M
Kainate receptors &Development-Minority FellowshipF31NS049964 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JOSEPH, DONALD · 2004 to 2006
$136k
NINDS NIH HHS F31 NS049964NINDS NIH HHS NS053575NINDS NIH HHS NS49964NINDS NIH HHS R01 NS029797NINDS NIH HHS R01 NS053575
6 · The paper itself

Abstract

Neurite outgrowth is a fundamental step in establishing proper neuronal connections in the developing central nervous system. Dynamic control of outgrowth has been attributed to changes in growth cone Ca2+ levels in response to extracellular cues. Here we have investigated a possible role for Ca2+ permeable kainate (KA) receptors in regulating neurite outgrowth of nociceptive-like dorsal root ganglion (DRG) neurons. To identify KA receptor subunits likely to be involved, we used quantitative RT-PCR on acutely dissociated DRG and dorsal horn neurons. DRG neurons expressed more GluK1, particularly the GluK1b spice variant, than dorsal horn neurons. Conversely, dorsal horn neurons expressed more GluK2, particularly GluK2a, than DRG neurons. Further, an RNA editing assay indicated that the majority of GluK1 and GluK2 mRNA transcripts in DRG were unedited. Imaging Ca2+ transients following application of a KA receptor agonist to DRG and dorsal horn co-cultures revealed increases in intracellular Ca2+ in the growth cones of DRG neurons. In the majority of cases, this increase in Ca2+ was partly or completely blocked by Joro spider toxin (JSTX), an antagonist for Ca2+-permeable AMPA and KA receptors. Treatment of DRG/dorsal horn co-cultures with KA for 18 hours suppressed neurite outgrowth while application of the rapidly desensitizing KA receptor agonist SYM 2081, the competitive AMPA/KA receptor antagonist, CNQX, and JSTX or philanthotoxin enhanced neurite outgrowth and prevented KA effects on neurite outgrowth. Thus, Ca2+ entry through KA receptors at the growth cone of DRG neurons may be an important regulator of neurite outgrowth.

Indexed as

6-Cyano-7-nitroquinoxaline-2,3-dioneAdenosine DeaminaseAnalysis of VarianceAnimalsCalciumCells, CulturedDose-Response Relationship, DrugEmbryo, MammalianExcitatory Amino Acid AntagonistsGanglia, SpinalGAP-43 ProteinGene Expression RegulationGluK2 Kainate ReceptorGlutamatesGrowth ConesKainic Acid4-methylglutamic acid6-Cyano-7-nitroquinoxaline-2,3-dioneAda protein, ratAdenosine DeaminaseCalciumdomoic acidExcitatory Amino Acid AntagonistsGAP-43 ProteinGluK2 Kainate ReceptorGlutamatesJSTX spider toxinKainic AcidKainic Acid ReceptorsMembrane ProteinsNeuromuscular Depolarizing AgentsRNA, MessengerSpider Venoms

Identifiers

PMID21557511
PMCPMC3973019
OpenAlexW1987198820

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.