Evidence map›Paper›PMID 25814934›Full record

ArticleFrontiers in cellular neuroscience2015

Brain region-specific gene expression profiles in freshly isolated rat microglia.

Karlijn J Doorn, John J P Brevé, Benjamin Drukarch, Hendrikus W Boddeke, Inge Huitinga, Paul J Lucassen, Anne-Marie van Dam

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 106 citations in OpenAlex.

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  16. An emerging role for microglia in stress-effects on memory.The European journal of neuroscience · 2022
    Review
  17. Article
  18. Article
  19. Review
  20. Microglia and Microglia-Like Cells: Similar but Different.Frontiers in cellular neuroscience · 2022
    Review

4 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Karlijn J DoornDepartment Structural and Functional Plasticity of the Nervous System, Center for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, Netherlands ; Neuroscience Campus Amsterdam, Department Anatomy and Neurosciences, VU University Medical Center Amsterdam, Netherlands.
John J P BrevéNeuroscience Campus Amsterdam, Department Anatomy and Neurosciences, VU University Medical Center Amsterdam, Netherlands.
Benjamin DrukarchNeuroscience Campus Amsterdam, Department Anatomy and Neurosciences, VU University Medical Center Amsterdam, Netherlands.
Hendrikus W BoddekeSection Medical Physiology, Department of Neuroscience, University Medical Centre Groningen Groningen, Netherlands.
Inge HuitingaNeuroimmunology Group, Netherlands Institute for Neuroscience, Institute of the Royal Netherlands Academy of Arts and Sciences Amsterdam, Netherlands.
Paul J LucassenDepartment Structural and Functional Plasticity of the Nervous System, Center for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, Netherlands.
Anne-Marie van DamDepartment Structural and Functional Plasticity of the Nervous System, Center for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, Netherlands.
Amsterdam Neuroscience · NLNetherlands Institute for Neuroscience · NLUniversity Medical Center Groningen · NLUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia are important cells in the brain that can acquire different morphological and functional phenotypes dependent on the local situation they encounter. Knowledge on the region-specific gene signature of microglia may hold valuable clues for microglial functioning in health and disease, e.g., Parkinson's disease (PD) in which microglial phenotypes differ between affected brain regions. Therefore, we here investigated whether regional differences exist in gene expression profiles of microglia that are isolated from healthy rat brain regions relevant for PD. We used an optimized isolation protocol based on a rapid isolation of microglia from discrete rat gray matter regions using density gradients and fluorescent-activated cell sorting. Application of the present protocol followed by gene expression analysis enabled us to identify subtle differences in region-specific microglial expression profiles and show that the genetic profile of microglia already differs between different brain regions when studied under control conditions. As such, these novel findings imply that brain region-specific microglial gene expression profiles exist that may contribute to the region-specific differences in microglia responsivity during disease conditions, such as seen in, e.g., PD.

Indexed as

FACShippocampusmicrogliaolfactory bulbParkinson’s diseasesubstantia nigra

Identifiers

PMID25814934
PMCPMC4357261
OpenAlexW2162188109

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.