Evidence map›Paper›PMID 22157653›Full record

ArticleCell research2012

Endosome-mediated retrograde axonal transport of P2X3 receptor signals in primary sensory neurons.

Xu-Qiao Chen, Bin Wang, Chengbiao Wu, Jin Pan, Bo Yuan, Yuan-Yuan Su, Xing-Yu Jiang, Xu Zhang, Lan Bao

Open access · bronzeAbstract read
In one paragraph

Article in Cell research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
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  11. Article
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  13. Article
  14. The effect of spinal cord injury on the neurochemical properties of vagal sensory neurons.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  15. Article
  16. Article
  17. ATP P2X3 receptors and neuronal sensitization.Frontiers in cellular neuroscience · 2013
    Review
  18. Article
  19. KIF5B promotes the forward transport and axonal function of the voltage-gated sodium channel Nav1.8.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  20. 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

9 authors at 5 institutions in 2 countries.

Xu-Qiao ChenState Key Laboratory of Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Bin Wang
Chengbiao Wu
Jin Pan
Bo Yuan
Yuan-Yuan Su
Xing-Yu Jiang
Xu Zhang
Lan Bao
Center for Excellence in Molecular Cell Science · CNChinese Academy of Sciences · CNNational Center for Nanoscience and Technology · CNShanghai Institutes for Biological Sciences · CNUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotrophins and their receptors adopt signaling endosomes to transmit retrograde signals. However, the mechanisms of retrograde signaling for other ligand/receptor systems are poorly understood. Here, we report that the signals of the purinergic (P)2X(3) receptor, an ATP-gated ion channel, are retrogradely transported in dorsal root ganglion (DRG) neuron axons. We found that Rab5, a small GTPase, controls the early sorting of P2X(3) receptors into endosomes, while Rab7 mediates the fast retrograde transport of P2X(3) receptors. Intraplantar injection and axonal application into the microfluidic chamber of α, β-methylene-ATP (α, β-MeATP), a P2X selective agonist, enhanced the endocytosis and retrograde transport of P2X(3) receptors. The α, β-MeATP-induced Ca(2+) influx activated a pathway comprised of protein kinase C, rat sarcoma viral oncogene and extracellular signal-regulated protein kinase (ERK), which associated with endocytic P2X(3) receptors to form signaling endosomes. Disruption of the lipid rafts abolished the α, β-MeATP-induced ERK phosphorylation, endocytosis and retrograde transport of P2X(3) receptors. Furthermore, treatment of peripheral axons with α, β-MeATP increased the activation level of ERK and cAMP response element-binding protein in the cell bodies of DRG neurons and enhanced neuronal excitability. Impairment of either microtubule-based axonal transport in vivo or dynein function in vitro blocked α, β-MeATP-induced retrograde signals. These results indicate that P2X(3) receptor-activated signals are transmitted via retrogradely transported endosomes in primary sensory neurons and provide a novel signaling mechanism for ligand-gated channels.

Indexed as

MAP Kinase Signaling SystemAnimalsAxonal TransportCyclic AMP Response Element-Binding ProteinEndocytosisEndosomesGanglia, SpinalHEK293 CellsHumansLigandsMembrane MicrodomainsPhosphorylationProtein Kinase CRatsRats, Sprague-DawleyReceptors, Purinergic P2X3Cyclic AMP Response Element-Binding ProteinLigandsProtein Kinase CReceptors, Purinergic P2X3

Identifiers

PMID22157653
PMCPMC3317558
OpenAlexW1971504915

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.