Evidence map›Paper›PMID 31998844›Full record

ArticleScience advances2020

Microglia response following acute demyelination is heterogeneous and limits infiltrating macrophage dispersion.

Jason R Plemel, Jo Anne Stratton, Nathan J Michaels, Khalil S Rawji, Eric Zhang, Sarthak Sinha, Charbel S Baaklini, Yifei Dong, Madelene Ho, Kevin Thorburn and 13 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 2 pooled it
13.2field-weighted citation impact, top 1% 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

126 citing papers in PubMed, 2 syntheses or guidelines pooled it, 206 citations in OpenAlex.

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  16. Astrocytic ET-1 System Determines Microglia Phenotype Following Spinal Cord Injury.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  17. Review
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66 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

23 authors at 2 institutions in 1 country.

Jason R PlemelHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0003-1385-1464
Jo Anne StrattonHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-1205-1353
Nathan J MichaelsHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Khalil S RawjiHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-9687-8330
Eric ZhangHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-1268-5073
Sarthak SinhaDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-0770-3150
Charbel S BaakliniNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-1075-0767
Yifei DongHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Madelene HoNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Kevin ThorburnDepartment of Pharmacology, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-6996-2561
Timothy N FriedmanNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-0058-5075
Sana JawadHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Claudia SilvaHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Andrew V CaprarielloHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-2529-5621
Vahid HoghooghiHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Julie YueNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Arzina JafferDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-9197-9060
Kelly LeeNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-5027-1146
Bradley J KerrNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-0264-8316
Raj MidhaHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Peter K StysHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Jeff BiernaskieHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-0633-0698
V Wee YongHotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-2600-3563
University of Calgary · CAUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia and infiltrating macrophages are thought to orchestrate the central nervous system (CNS) response to injury; however, the similarities between these cells make it challenging to distinguish their relative contributions. We genetically labeled microglia and CNS-associated macrophages to distinguish them from infiltrating macrophages. Using single-cell RNA sequencing, we describe multiple microglia activation states, one of which was enriched for interferon associated signaling. Although blood-derived macrophages acutely infiltrated the demyelinated lesion, microglia progressively monopolized the lesion environment where they surrounded infiltrating macrophages. In the microglia-devoid sciatic nerve, the infiltrating macrophage response was sustained. In the CNS, the preferential proliferation of microglia and sparse microglia death contributed to microglia dominating the lesion. Microglia ablation reversed the spatial restriction of macrophages with the demyelinated spinal cord, highlighting an unrealized macrophages-microglia interaction. The restriction of peripheral inflammation by microglia may be a previously unidentified mechanism by which the CNS maintains its "immune privileged" status.

Indexed as

ApoptosisBiomarkersCell ProliferationCentral Nervous SystemComputational BiologyDemyelinating DiseasesFluorescent Antibody TechniqueGene Expression ProfilingMacrophage ActivationMacrophagesMicrogliaTranscriptomeBiomarkers

Identifiers

PMID31998844
PMCPMC6962036
OpenAlexW3000185208

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.