Evidence map›Paper›PMID 23171280›Full record

ArticleBMC neuroscience2012

Functional crosstalk in culture between macrophages and trigeminal sensory neurons of a mouse genetic model of migraine.

Alessia Franceschini, Asha Nair, Tanja Bele, Arn Mjm van den Maagdenberg, Andrea Nistri, Elsa Fabbretti

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 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
2.5field-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, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Role of ATP in migraine mechanisms: focus on P2X3 receptors.The journal of headache and pain · 2023
    Review
  5. Dural Immune Cells, CGRP, and Migraine.Frontiers in neurology · 2022
    Review
  6. Review
  7. Cross-talk signaling in the trigeminal ganglion: role of neuropeptides and other mediators.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  8. Current understanding of trigeminal ganglion structure and function in headache.Cephalalgia : an international journal of headache · 2019
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. ATP P2X3 receptors and neuronal sensitization.Frontiers in cellular neuroscience · 2013
    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

6 authors at 3 institutions in 3 countries.

Alessia FranceschiniDepartment of Neuroscience and Italian Institute of Technology Unit, International School for Advanced Studies (SISSA), Via Bonomea 265, Trieste, 34136, Italy.
Asha Nair
Tanja Bele
Arn Mjm van den Maagdenberg
Andrea Nistri
Elsa Fabbretti
Italian Institute of Technology · ITLeiden University Medical Center · NLUniversity of Nova Gorica · SI

Funding

Telethon GGP10082
6 · The paper itself

Abstract

backgroundEnhanced activity of trigeminal ganglion neurons is thought to underlie neuronal sensitization facilitating the onset of chronic pain attacks, including migraine. Recurrent headache attacks might establish a chronic neuroinflammatory ganglion profile contributing to the hypersensitive phenotype. Since it is difficult to study this process in vivo, we investigated functional crosstalk between macrophages and sensory neurons in primary cultures from trigeminal sensory ganglia of wild-type (WT) or knock-in (KI) mice expressing the Cacna1a gene mutation (R192Q) found in familial hemiplegic migraine-type 1. After studying the number and morphology of resident macrophages in culture, the consequences of adding host macrophages on macrophage phagocytosis and membrane currents mediated by pain-transducing P2X3 receptors on sensory neurons were examined.

resultsKI ganglion cultures constitutively contained a larger number of active macrophages, although no difference in P2X3 receptor expression was found. Co-culturing WT or KI ganglia with host macrophages (active as much as resident cells) strongly stimulated single cell phagocytosis. The same protocol had no effect on P2X3 receptor expression in WT or KI co-cultures, but it largely enhanced WT neuron currents that grew to the high amplitude constitutively seen for KI neurons. No further potentiation of KI neuronal currents was observed.

conclusionsTrigeminal ganglion cultures from a genetic mouse model of migraine showed basal macrophage activation together with enhanced neuronal currents mediated by P2X3 receptors. This phenotype could be replicated in WT cultures by adding host macrophages, indicating an important functional crosstalk between macrophages and sensory neurons.

Indexed as

Adenosine TriphosphateAnimalsAnimals, NewbornCalcium-Binding ProteinsCalcium Channels, L-TypeCell CommunicationCells, CulturedCoculture TechniquesMacrophagesMembrane PotentialsMiceMice, Inbred C57BLMice, TransgenicMicrofilament ProteinsMutationPatch-Clamp TechniquesAdenosine TriphosphateAif1 protein, mousealpha,beta-methyleneadenosine 5'-triphosphatebeta3 tubulin, mouseCACNA1C protein, mouseCalcium-Binding ProteinsCalcium Channels, L-TypeMicrofilament ProteinsReceptors, Purinergic P2X3Tubulin

Identifiers

PMID23171280
PMCPMC3511260
OpenAlexW1971635159

What OpenQuestion holds

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LicenceCC BY
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.