Evidence map›Paper›PMID 31212874›Full record

ArticleCells2019

Distinct Protein Expression Networks are Activated in Microglia Cells after Stimulation with IFN-γ and IL-4.

Daniele Vergara, Annamaria Nigro, Alessandro Romano, Stefania De Domenico, Marina Damato, Julien Franck, Chiara Coricciati, Maxence Wistorski, Tristan Cardon, Isabelle Fournier and 4 more

Abstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Asiatic Acid Attenuates Inflammation Induced byInternational journal of molecular sciences · 2022
    Article
  11. Immunometabolic Modulatory Role of Naltrexone in BV-2 Microglia Cells.International journal of molecular sciences · 2021
    Article
  12. Heparanome-Mediated Rescue of Oligodendrocyte Progenitor Quiescence following Inflammatory Demyelination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. 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

14 authors.

Daniele VergaraDepartment of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy. daniele.vergara@unisalento.it.ORCID 0000-0002-2396-7674
Annamaria NigroDivision of Neuroscience, Institute of Experimental Neurology-IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy. nigro.annamaria@hsr.it.ORCID 0000-0001-9570-7276
Alessandro RomanoDivision of Neuroscience, Institute of Experimental Neurology-IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy. romano.alessandro@hsr.it.
Stefania De DomenicoInstitute of Food Production Sciences, C.N.R. Unit of Lecce, 73100 Lecce, Italy. stefaniadedomenico@yahoo.it.ORCID 0000-0002-3501-5881
Marina DamatoDepartment of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy. marina.damato@hotmail.it.
Julien FranckU1192 INSERM, Laboratoire PRISM: Protéomique, Réponse Inflammatoire, Spectrométrie de Masse, Université de Lille, F-59000 Lille, France. julien.franck@univ-lille.fr.
Chiara CoricciatiDepartment of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy. chiara-crc@libero.it.
Maxence WistorskiU1192 INSERM, Laboratoire PRISM: Protéomique, Réponse Inflammatoire, Spectrométrie de Masse, Université de Lille, F-59000 Lille, France. maxence.wisztorski@univ-lille.fr.ORCID 0000-0003-1320-075X
Tristan CardonU1192 INSERM, Laboratoire PRISM: Protéomique, Réponse Inflammatoire, Spectrométrie de Masse, Université de Lille, F-59000 Lille, France. cardon.tristan@yahoo.fr.
Isabelle FournierU1192 INSERM, Laboratoire PRISM: Protéomique, Réponse Inflammatoire, Spectrométrie de Masse, Université de Lille, F-59000 Lille, France. isabelle.fournier@univ-lille.fr.
Angelo QuattriniDivision of Neuroscience, Institute of Experimental Neurology-IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy. quattrini.angelo@hsr.it.ORCID 0000-0002-8226-8320
Michel SalzetU1192 INSERM, Laboratoire PRISM: Protéomique, Réponse Inflammatoire, Spectrométrie de Masse, Université de Lille, F-59000 Lille, France. michel.salzet@univ-lille.fr.ORCID 0000-0003-4318-0817
Roberto FurlanDivision of Neuroscience, Institute of Experimental Neurology-IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy. furlan.roberto@hsr.it.ORCID 0000-0001-7376-9425
Michele MaffiaDepartment of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy. michele.maffa@unisalento.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia cells are the primary immune population of the central nervous system with a role in the regulation of several physiological and pathological conditions. Upon appropriate stimulation, microglia cells can be polarized in a pro-inflammatory M1-like or anti-inflammatory M2-like status. Biological processes and pathways engaged in microglia polarization are starting to be elucidated. To help clarify this, we used a liquid chromatography-mass spectrometry (LC-MS/MS) label free approach to characterize the proteomic profile of human microglia cell line (CHME-5) stimulated with gamma-interferon (IFN-γ) and interleukin-4 (IL-4) to induce a M1 or M2 phenotype, respectively. Outside the classical M1/M2 polarization markers, the M1 status appears to center around the activation of a classical inflammatory response and through the activation of multiple signaling pathways. M2 polarization resulted in a different pattern of protein modulation related to RNA and cellular metabolic processes. Together, our findings provide information regarding the protein changes specific to M1 and M2 activation states, and potentially link the polarization of microglia cells to the acquisition of a specific proteomic profile.

Indexed as

Cell LineHumansInterferon-gammaInterleukin-4Macrophage ActivationMetabolic Networks and PathwaysMicrogliaPhenotypeProteinsProteomicsSignal TransductionTranscription, GeneticInterferon-gammaInterleukin-4ProteinsIFN-γIL-4mass spectrometrymicrogliamicroglia plasticityproteomics

Identifiers

PMID31212874
PMCPMC6628119

What OpenQuestion holds

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LicenceCC BY
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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.