Evidence map›Paper›PMID 25762685›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Immune quiescence of the brain is set by astroglial connexin 43.

Anne-Cécile Boulay, Aurélien Mazeraud, Salvatore Cisternino, Bruno Saubaméa, Phillipe Mailly, Laurent Jourdren, Corinne Blugeon, Virginie Mignon, Maria Smirnova, Alessia Cavallo and 7 more

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Review
  2. Review
  3. Development of perivascular astrocyte processes.Frontiers in neuroscience · 2025
    Review
  4. Article
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  6. Review
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  8. Article
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  15. Review
  16. Astroglial Connexins in Neurodegenerative Diseases.Frontiers in molecular neuroscience · 2021
    Review
  17. Article
  18. Article
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  20. Review
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

17 authors.

Anne-Cécile BoulayCollege of France, Center for Interdisciplinary Research in Biology/National Center of Scientific Research (CNRS), Coeducational Research Unit (UMR) 7241, National Institute of Health and Medical Research (INSERM), U1050/Neuroglial Interactions in Cerebral Physiopathology, F-75231 Paris, France, University Pierre and Marie Curie, F-75005 Paris, France, MemoLife Laboratory of Excellence and Paris Science Lettre Research University, F-75005 Paris, France.
Aurélien MazeraudHuman Histopathology and Animal Models and Paris Descartes University-Sorbonne Paris Cité and Neuropathology Service, Sainte-Anne Hospital Center, F-75014 Paris, France.ORCID http://orcid.org/0000-0001-8473-7779
Salvatore CisterninoFaculté de Pharmacie, UMR in Health 1144, F-75006 Paris, France, Psychotropic Response Variability, INSERM, U1144, Paris, F-75006, France, Paris Diderot University, Coeducational Research Unit in Health 1144, F-75013 Paris, France.
Bruno SaubaméaFaculté de Pharmacie, UMR in Health 1144, F-75006 Paris, France, Psychotropic Response Variability, INSERM, U1144, Paris, F-75006, France, Paris Diderot University, Coeducational Research Unit in Health 1144, F-75013 Paris, France.
Phillipe MaillyCollege of France, Center for Interdisciplinary Research in Biology/National Center of Scientific Research (CNRS), Coeducational Research Unit (UMR) 7241, National Institute of Health and Medical Research (INSERM), U1050/Neuroglial Interactions in Cerebral Physiopathology, F-75231 Paris, France, University Pierre and Marie Curie, F-75005 Paris, France, MemoLife Laboratory of Excellence and Paris Science Lettre Research University, F-75005 Paris, France.
Laurent JourdrenEcole Normale Supérieure, Institute of Biology, Genomic Platform, F-75005 Paris, France, INSERM, U1024, F-75005 Paris, France, CNRS, UMR 8197, Paris, F-75005 France.
Corinne BlugeonEcole Normale Supérieure, Institute of Biology, Genomic Platform, F-75005 Paris, France, INSERM, U1024, F-75005 Paris, France, CNRS, UMR 8197, Paris, F-75005 France.
Virginie MignonFaculté de Pharmacie, UMR in Health 1144, F-75006 Paris, France, Psychotropic Response Variability, INSERM, U1144, Paris, F-75006, France, Paris Diderot University, Coeducational Research Unit in Health 1144, F-75013 Paris, France.
Maria SmirnovaFaculté de Pharmacie, UMR in Health 1144, F-75006 Paris, France, Psychotropic Response Variability, INSERM, U1144, Paris, F-75006, France, Paris Diderot University, Coeducational Research Unit in Health 1144, F-75013 Paris, France.
Alessia CavalloCollege of France, Center for Interdisciplinary Research in Biology/National Center of Scientific Research (CNRS), Coeducational Research Unit (UMR) 7241, National Institute of Health and Medical Research (INSERM), U1050/Neuroglial Interactions in Cerebral Physiopathology, F-75231 Paris, France, University Pierre and Marie Curie, F-75005 Paris, France, MemoLife Laboratory of Excellence and Paris Science Lettre Research University, F-75005 Paris, France.
Pascal EzanCollege of France, Center for Interdisciplinary Research in Biology/National Center of Scientific Research (CNRS), Coeducational Research Unit (UMR) 7241, National Institute of Health and Medical Research (INSERM), U1050/Neuroglial Interactions in Cerebral Physiopathology, F-75231 Paris, France, University Pierre and Marie Curie, F-75005 Paris, France, MemoLife Laboratory of Excellence and Paris Science Lettre Research University, F-75005 Paris, France.
Patrick AvéHuman Histopathology and Animal Models and Paris Descartes University-Sorbonne Paris Cité and Neuropathology Service, Sainte-Anne Hospital Center, F-75014 Paris, France.
Florent DingliCurie Institute Research Center, Protein Mass Spectrometry Laboratory, F-75248 Paris, France, and.ORCID http://orcid.org/0000-0002-7715-2446
Damarys LoewCurie Institute Research Center, Protein Mass Spectrometry Laboratory, F-75248 Paris, France, and.
Paulo VieiraLymphopoiesis Unit, Pasteur Institute, F-75015 Paris, France, INSERM, U668, F-75015 Paris, France.
Fabrice ChrétienHuman Histopathology and Animal Models and Paris Descartes University-Sorbonne Paris Cité and Neuropathology Service, Sainte-Anne Hospital Center, F-75014 Paris, France.
Martine Cohen-SalmonCollege of France, Center for Interdisciplinary Research in Biology/National Center of Scientific Research (CNRS), Coeducational Research Unit (UMR) 7241, National Institute of Health and Medical Research (INSERM), U1050/Neuroglial Interactions in Cerebral Physiopathology, F-75231 Paris, France, University Pierre and Marie Curie, F-75005 Paris, France, MemoLife Laboratory of Excellence and Paris Science Lettre Research University, F-75005 Paris, France, martine.cohen-salmon@college-de-france.fr.ORCID http://orcid.org/0000-0002-5312-8476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the normal brain, immune cell trafficking and immune responses are strictly controlled and limited. This unique homeostatic equilibrium, also called brain immune quiescence, is crucial to maintaining proper brain functions and is altered in various pathological processes, from chronic immunopathological disorders to cognitive and psychiatric impairments. To date, the precise nature of factors regulating the brain/immune system interrelationship is poorly understood. In the present study, we demonstrate that one of these regulating factors is Connexin 43 (Cx43), a gap junction protein highly expressed by astrocytes at the blood-brain barrier (BBB) interface. We show that, by setting the activated state of cerebral endothelium, astroglial Cx43 controls immune recruitment as well as antigen presentation mechanisms in the mouse brain. Consequently, in the absence of astroglial Cx43, recruited immune cells elaborate a specific humoral autoimmune response against the von Willebrand factor A domain-containing protein 5a, an extracellular matrix protein of the brain. Altogether, our results demonstrate that Cx43 is a new astroglial factor promoting the immune quiescence of the brain.

Indexed as

Age FactorsAlbuminsAnimalsAstrocytesBlood-Brain BarrierBrainCalcium-Binding ProteinsCarbon IsotopesCD3 ComplexCell MovementCells, CulturedConnexin 43CytokinesEndothelial CellsFemaleGlial Fibrillary Acidic ProteinAif1 protein, mouseAlbuminsCalcium-Binding ProteinsCarbon IsotopesCD3 ComplexConnexin 43CytokinesGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseMicrofilament ProteinsNerve Tissue ProteinsS100 ProteinsSucroseastrocyteautoimmunityblood-brain barrierconnexinimmune quiescence

Identifiers

PMID25762685
PMCPMC6605289

What OpenQuestion holds

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Registered trials

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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.