Evidence map›Paper›PMID 26124113›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Notch1-STAT3-ETBR signaling axis controls reactive astrocyte proliferation after brain injury.

Matthew D LeComte, Issei S Shimada, Casey Sherwin, Jeffrey L Spees

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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
6.5field-weighted citation impact, top 3% 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, 94 citations in OpenAlex.

  1. Article
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  10. BQ788 reveals glial ETBritish journal of pharmacology · 2023
    Article
  11. Review
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  13. Article
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  15. Lunatic Fringe-GFP Marks Lamina-Specific Astrocytes That Regulate Sensory Processing.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  16. Article
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  18. Review
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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

4 authors at 1 institution in 1 country.

Matthew D LeComteDepartment of Medicine, Stem Cell Core, University of Vermont, Colchester, VT 05446; Department of Neurological Sciences, University of Vermont, Burlington, VT 05401; Neuroscience Graduate Program, University of Vermont, Burlington, VT 05401.ORCID http://orcid.org/0000-0001-7703-9729
Issei S ShimadaDepartment of Medicine, Stem Cell Core, University of Vermont, Colchester, VT 05446;
Casey SherwinDepartment of Medicine, Stem Cell Core, University of Vermont, Colchester, VT 05446; Department of Neurological Sciences, University of Vermont, Burlington, VT 05401; Neuroscience Graduate Program, University of Vermont, Burlington, VT 05401.
Jeffrey L SpeesDepartment of Medicine, Stem Cell Core, University of Vermont, Colchester, VT 05446; Department of Neurological Sciences, University of Vermont, Burlington, VT 05401; Neuroscience Graduate Program, University of Vermont, Burlington, VT 05401 jeffrey.spees@uvm.edu.
University of Vermont · US

Funding

Control of reactive astrocytes by Notch1 and Amyloid Precursor ProteinR01NS073815 · NINDS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI SPEES, JEFFREY L · 2012 to 2015
$1.3M
NINDS NIH HHS R01 NS073815NINDS NIH HHS R01NS073815
6 · The paper itself

Abstract

Defining the signaling network that controls reactive astrogliosis may provide novel treatment targets for patients with diverse CNS injuries and pathologies. We report that the radial glial cell antigen RC2 identifies the majority of proliferating glial fibrillary acidic protein-positive (GFAP(+)) reactive astrocytes after stroke. These cells highly expressed endothelin receptor type B (ETB(R)) and Jagged1, a Notch1 receptor ligand. To study signaling in adult reactive astrocytes, we developed a model based on reactive astrocyte-derived neural stem cells isolated from GFAP-CreER-Notch1 conditional knockout (cKO) mice. By loss- and gain-of-function studies and promoter activity assays, we found that Jagged1/Notch1 signaling increased ETB(R) expression indirectly by raising the level of phosphorylated signal transducer and activator of transcription 3 (STAT3), a previously unidentified EDNRB transcriptional activator. Similar to inducible transgenic GFAP-CreER-Notch1-cKO mice, GFAP-CreER-ETB(R)-cKO mice exhibited a defect in reactive astrocyte proliferation after cerebral ischemia. Our results indicate that the Notch1-STAT3-ETB(R) axis connects a signaling network that promotes reactive astrocyte proliferation after brain injury.

Indexed as

Cell ProliferationSignal TransductionAnimalsAstrocytesBrain InjuriesMaleMiceMice, Inbred C57BLMice, KnockoutPromoter Regions, GeneticReceptor, Endothelin BReceptor, Notch1STAT3 Transcription FactorNotch1 protein, mouseReceptor, Endothelin BReceptor, Notch1Stat3 protein, mouseSTAT3 Transcription FactorETBRNotch1proliferationreactive astrocyteSTAT3

Identifiers

PMID26124113
PMCPMC4507218
OpenAlexW1642543027

What OpenQuestion holds

Textmetadata
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.