Evidence map›Paper›PMID 29790106›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2018

Imaging Reporter Strategy to Monitor Gene Activation of Microglia Polarisation States under Stimulation.

Franziska M Collmann, Rory Pijnenburg, Gabriele Schneider, Cordula Schäfer, Kat Folz-Donahue, Christian Kukat, Mathias Hoehn

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. IndividualFrontiers in immunology · 2019
    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 3 institutions in 2 countries.

Franziska M CollmannMax Planck Institute for Metabolism Research, In-vivo-NMR Laboratory, Gleueler Straße 50, D-50931, Cologne, Germany.
Rory PijnenburgMax Planck Institute for Metabolism Research, In-vivo-NMR Laboratory, Gleueler Straße 50, D-50931, Cologne, Germany.
Gabriele SchneiderMax Planck Institute for Metabolism Research, In-vivo-NMR Laboratory, Gleueler Straße 50, D-50931, Cologne, Germany.
Cordula SchäferMax Planck Institute for Metabolism Research, In-vivo-NMR Laboratory, Gleueler Straße 50, D-50931, Cologne, Germany.
Kat Folz-DonahueMax Planck Institute for Biology of Ageing, FACS & Imaging Core Facility, Cologne, Germany.
Christian KukatMax Planck Institute for Biology of Ageing, FACS & Imaging Core Facility, Cologne, Germany.
Mathias HoehnMax Planck Institute for Metabolism Research, In-vivo-NMR Laboratory, Gleueler Straße 50, D-50931, Cologne, Germany. mathias@sf.mpg.de.
Max Planck Institute for Metabolism Research · DEMax Planck Institute for Biology of Ageing · DEPercuros (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglial cells as innate immune key players have a critical and unique role in neurodegenerative disorders. They strongly interact with their microenvironment in a complex manner and react to changes by switching their phenotype and functional activation states. In order to understand the development of brain diseases, it is imperative to elucidate up- or down-regulation of genes involved in microglia polarisation in time-profile by a simple-to-use strategy. Here, we present a new imaging strategy to follow promoter activity of genes involved in microglia polarisation. We lentivirally transduced BV-2 microglia cells in culture with constructs consisting of the induced nitric oxide synthase (iNOS), Fc gamma receptor III (Fcgr3) (both resembling the pro-inflammatory M1-like phenotype) or Chitinase-like 3 (Chil3/Ym1) (resembling the anti-inflammatory M2-like phenotype) promoters and stimulated transgenic cells with potent activators for pro- or anti-inflammatory response, such as lipopolysaccharide (LPS) + interferon gamma (IFN-γ) or interleukin (IL)-4, respectively. Promoter activities upon polarisation phases were quantitatively assessed by the two imaging reporters Luc2 for bioluminescence and eGFP for fluorescence.

Indexed as

AnimalsAnti-Inflammatory Agentsbeta-N-AcetylhexosaminidasesCell PolarityCells, CulturedGenes, ReporterGenetic VectorsImage Processing, Computer-AssistedLectinsLentivirusMiceMicrogliaMicroscopy, FluorescenceNitric Oxide Synthase Type IIReceptors, IgGTranscriptional ActivationAnti-Inflammatory Agentsbeta-N-AcetylhexosaminidasesChil3 protein, mouseFcgr3 protein, mouseLectinsNitric Oxide Synthase Type IINos2 protein, mouseReceptors, IgGBioluminescence imagingFluorescence imagingMicrogliaMicroglia polarisationReporter imaging

Identifiers

PMID29790106
PMCPMC6096558
OpenAlexW2804097999

What OpenQuestion holds

Textmetadata
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.