Evidence map›Paper›PMID 25053164›Full record

ArticleJournal of cellular biochemistry2014

Autotaxin downregulates LPS-induced microglia activation and pro-inflammatory cytokines production.

Rana Awada, Jean Sébastien Saulnier-Blache, Sandra Grès, Emmanuel Bourdon, Philippe Rondeau, Avinash Parimisetty, Ruben Orihuela, G Jean Harry, Christian Lefebvre d'Hellencourt

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 60 citations in OpenAlex.

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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 4 institutions in 2 countries.

Rana AwadaGroupe d'Etude sur l'Inflammation Chronique et l'Obésité (GEICO) EA 4516, Université de La Réunion, 15 avenue R. Cassin, CS 92003, 97715, Saint Denis Cedex and Plateforme CYROI, 2 Rue Maxime Rivière, BP 80 005, Sainte Clotilde Cedex, Reunion Island, France.
Jean Sébastien Saulnier-Blache
Sandra Grès
Emmanuel Bourdon
Philippe Rondeau
Avinash Parimisetty
Ruben Orihuela
G Jean Harry
Christian Lefebvre d'Hellencourt
Inserm · FRInstitut des Maladies Métaboliques et Cardiovasculaires · FRNational Institute of Environmental Health Sciences · USNational Institutes of Health · US

Funding

Environmentally Induced Alterations In Neuron And Glia Development and AgingZIAES021164 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI HARRY, GAYLIA JEAN · 2009 to 2021
$15.4M
Environment Effects and Development of Neuron and GliaZ01ES021164 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI HARRY, GAYLIA JEAN · 1997 to 2008
$409k
Intramural NIH HHS Z01 ES021164
6 · The paper itself

Abstract

Inflammation is essential in defense against infection or injury. It is tightly regulated, as over-response can be detrimental, especially in immune-privileged organs such as the central nervous system (CNS). Microglia constitutes the major source of inflammatory factors, but are also involved in the regulation of the inflammation and in the reparation. Autotaxin (ATX), a phospholipase D, converts lysophosphatidylcholine (LPC) into lysophosphatidic acid (LPA) and is upregulated in several CNS injuries. LPA, a pleiotropic immunomodulatory factor, can induce multiple cellular processes including morphological changes, proliferation, death, and survival. We investigated ATX effects on microglia inflammatory response to lipopolysaccharide (LPS), mimicking gram-negative infection. Murine BV-2 microglia and stable transfected, overexpressing ATX-BV-2 (A +) microglia were treated with LPS. Tumor necrosis factor α (TNFα), interleukin (IL)-6, and IL-10 mRNA and proteins levels were examined by qRT-PCR and ELISA, respectively. Secreted LPA was quantified by a radioenzymatic assay and microglial activation markers (CD11b, CD14, B7.1, and B7.2) were determined by flow cytometry. ATX expression and LPA production were significantly enhanced in LPS treated BV-2 cells. LPS induction of mRNA and protein level for TNFα and IL-6 were inhibited in A+ cells, while IL-10 was increased. CD11b, CD14, and B7.1, and B7.2 expressions were reduced in A+ cells. Our results strongly suggest deactivation of microglia and an IL-10 inhibitory of ATX with LPS induced microglia activation.

Indexed as

AnimalsAntigens, CDCell LineDown-RegulationGene ExpressionInterleukin-10Interleukin-6LipopolysaccharidesLysophospholipase DLysophospholipidsMiceMicrogliaNF-kappa BPhosphoric Diester HydrolasesTranscriptional ActivationTranscription Factor AP-1Antigens, CDIL10 protein, mouseInterleukin-10Interleukin-6Lipopolysaccharideslysophosphatidic acidLysophospholipase DLysophospholipidsNF-kappa BPhosphoric Diester HydrolasesTranscription Factor AP-1Tumor Necrosis Factor-alphaAUTOTAXININFLAMMATIONLYSOPHOSPHATIDIC ACIDMICROGLIA

Identifiers

PMID25053164
PMCPMC4275303
OpenAlexW1943915905

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.