Evidence map›Paper›PMID 24632419›Full record

ArticleNeurobiology of disease2014

Adenosine A2A receptor antagonism reverses inflammation-induced impairment of microglial process extension in a model of Parkinson's disease.

Stefka Gyoneva, Lauren Shapiro, Carlos Lazo, Ethel Garnier-Amblard, Yoland Smith, Gary W Miller, Stephen F Traynelis

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Novel and experimental therapeutics for the management of motor and non-motor Parkinsonian symptoms.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Review
  8. Adenosine AInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Review
  11. Effects of Compounds Isolated fromInternational journal of molecular sciences · 2022
    Article
  12. AMolecules (Basel, Switzerland) · 2022
    Article
  13. Expression of the Adenosine ABiomedicines · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Stefka GyonevaDepartment of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA; Graduate Division of Biological and Biomedical Sciences, Molecular and Systems Pharmacology Program, Emory University, Atlanta, GA 30322, USA. Electronic address: stefka.gyoneva@gmail.com.
Lauren ShapiroGraduate Division of Biological and Biomedical Sciences, Molecular and Systems Pharmacology Program, Emory University, Atlanta, GA 30322, USA.
Carlos LazoSchool of Public Health, Environmental Health, Emory University, Atlanta, GA 30322, USA.
Ethel Garnier-AmblardDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Yoland SmithYerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA; Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Gary W MillerDepartment of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA; School of Public Health, Environmental Health, Emory University, Atlanta, GA 30322, USA; Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Stephen F TraynelisDepartment of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Emory University · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 1985 to 2011
$114.0M
The Emory Alzheimer's Disease CenterP50AG025688 · NIA · EMORY UNIVERSITY · PI WALKER, LARY C · 2005 to 2019
$25.7M
Graduate and Postdoctoral Training in ToxicologyT32ES012870 · NIEHS · EMORY UNIVERSITY · PI Carmen Joseph Marsit · 2004 to 2026
$9.1M
ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI BASSELL, GARY J · 2008 to 2018
$6.8M
Udall Parkinson's Disease Center at Emory University: Circuitry to TherapyP50NS071669 · NINDS · EMORY UNIVERSITY · PI WICHMANN, THOMAS · 2010 to 2015
$6.8M
Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Functional Effects of Adenosine A2A Receptor Activation on MicrogliaF31NS076215 · NINDS · EMORY UNIVERSITY · PI GYONEVA, STEFKA IVANOVA · 2011 to 2012
$61k
NCRR NIH HHS P51 RR000165NCRR NIH HHS RR00165NIA NIH HHS P50 AG025688NIEHS NIH HHS T32 ES012870NIEHS NIH HHS T32ES12870NIGMS NIH HHS T32 GM008602NIGMS NIH HHS T32GM008602NIH HHS P51 OD011132NINDS NIH HHS F31 NS076215NINDS NIH HHS F31NS076215NINDS NIH HHS P30 NS055077NINDS NIH HHS P50 NS071669NINDS NIH HHS P50-NS071669
6 · The paper itself

Abstract

Microglia, the immune cells of the central nervous system, constantly survey the parenchyma in the healthy brain to maintain homeostasis. When a disturbance, such as cell death, results in ATP release in vivo, microglial processes respond by utilizing P2Y12 purinergic receptors to trigger extension toward the site of damage. Processes ultimately surround the injury site, preventing the spread of harmful cellular constituents and assisting with tissue repair. In contrast to the healthy brain, many neurodegenerative diseases, including Parkinson's disease, are characterized by the presence of neuroinflammation. Yet, the ability of microglia to respond to tissue damage under pro-inflammatory conditions has not been well studied. To assess the ability of microglia to respond to tissue injury and localized cell death in the context of Parkinson's disease, we performed confocal imaging of acute brain slices from mice with microglia-specific green fluorescent protein expression. Microglia in coronal slices containing the substantia nigra extend processes toward a mechanical injury in a P2Y12 receptor-dependent manner. However, microglia in mice treated for 5days with 20mg/kg/day 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) show significantly reduced process displacement toward the injury compared to microglia in control animals. Pre-treatment of slices from MPTP-injected mice with the A2A receptor-selective antagonist preladenant restores the ability of activated microglia to respond to tissue damage. These data support the hypothesis that chronic inflammation impedes microglial motility in response to further injury, such as cell death, and suggest that some aspects of the neuroprotection observed with adenosine A2A receptor antagonists may involve direct or indirect actions at microglia.

Indexed as

Adenosine A2 Receptor AntagonistsAnimalsDisease Models, AnimalInflammationLipopolysaccharidesMiceMice, Inbred C57BLMicrogliaMPTP PoisoningSubstantia NigraAdenosine A2 Receptor AntagonistsLipopolysaccharidesAcute brain sliceAdenosine A(2A) receptorImagingMicrogliaNeuroinflammationParkinson's diseasePreladenant

Identifiers

PMID24632419
PMCPMC4072497
OpenAlexW2073992121

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.