Evidence map›Paper›PMID 25005116›Full record

ArticleJournal of neuroimmunology2014

Selective expression of Narp in primary nociceptive neurons: role in microglia/macrophage activation following nerve injury.

M Miskimon, S Han, J J Lee, M Ringkamp, M A Wilson, R S Petralia, X Dong, P F Worley, J M Baraban, I M Reti

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroimmunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pain and itch processing by subpopulations of molecularly diverse spinal and trigeminal projection neurons.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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

10 authors at 1 institution in 1 country.

M MiskimonDepartment of Neuroscience, Johns Hopkins University, United States.
S HanDepartment of Psychiatry, Johns Hopkins University, United States.
J J LeeDepartment of Psychiatry, Johns Hopkins University, United States.
M RingkampDepartment of Neurosurgery, Johns Hopkins University, United States.
M A WilsonDepartment of Neuroscience, Johns Hopkins University, United States.
R S PetraliaNIDCD, NIH, Johns Hopkins University, United States.
X DongDepartment of Neuroscience, Johns Hopkins University, United States.
P F WorleyDepartment of Neuroscience, Johns Hopkins University, United States.
J M BarabanDepartment of Neuroscience, Johns Hopkins University, United States; Department of Psychiatry, Johns Hopkins University, United States.
I M RetiDepartment of Neuroscience, Johns Hopkins University, United States; Department of Psychiatry, Johns Hopkins University, United States; Laboratory of Origin, United States. Electronic address: imreti@jhmi.edu.
Johns Hopkins University · US

Funding

Advanced Imaging CoreZICDC000081 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI WINKLER, DENNIS · 2012 to 2025
$17.4M
The Role of NARP in Drug AbuseR01DA016303 · NIDA · JOHNS HOPKINS UNIVERSITY · PI RETI, IRVING M · 2006 to 2013
$3.0M
Intramural NIH HHSNIDA NIH HHS R01 DA016303NIDA NIH HHS R01DA016303
6 · The paper itself

Abstract

Neuronal activity regulated pentraxin (Narp) is a secreted protein implicated in regulating synaptic plasticity via its association with the extracellular surface of AMPA receptors. We found robust Narp immunostaining in dorsal root ganglia (DRG) that is largely restricted to small diameter neurons, and in the superficial layers of the dorsal horn of the spinal cord. In double staining studies of DRG, we found that Narp is expressed in both IB4- and CGRP-positive neurons, markers of distinct populations of nociceptive neurons. Although a panel of standard pain behavioral assays were unaffected by Narp deletion, we found that Narp knockout mice displayed an exaggerated microglia/macrophage response in the dorsal horn of the spinal cord to sciatic nerve transection 3days after surgery compared with wild type mice. As other members of the pentraxin family have been implicated in regulating innate immunity, these findings suggest that Narp, and perhaps other neuronal pentraxins, also regulate inflammation in the nervous system.

Indexed as

AnimalsC-Reactive ProteinFemaleGanglia, SpinalGene ExpressionHyperalgesiaMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutMicrogliaNerve Tissue ProteinsNociceptorsPentraxinsPosterior Horn CellsC-Reactive ProteinNerve Tissue ProteinsPentraxinsAMPACGRPDorsal root ganglionInflammationPainPentraxin

Identifiers

PMID25005116
PMCPMC4152392
OpenAlexW2024845454

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.