Evidence map›Paper›PMID 31964978›Full record

ArticleScientific reports2020

Astrocyte Support for Oligodendrocyte Differentiation can be Conveyed via Extracellular Vesicles but Diminishes with Age.

Cory M Willis, Alexandra M Nicaise, Ernesto R Bongarzone, Maria Givogri, Cory R Reiter, Olivia Heintz, Evan R Jellison, Pearl A Sutter, Gregg TeHennepe, Guruprasad Ananda and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 72 citations in OpenAlex.

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  13. Astrocytic TIMP-1 regulates production of Anastellin, an inhibitor of oligodendrocyte differentiation and FTY720 responses.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  18. Lamin B1 as a key modulator of the developing and aging brain.Frontiers in cellular neuroscience · 2023
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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

12 authors at 3 institutions in 1 country.

Cory M WillisDepartment of Neuroscience, University of Connecticut School of Medicine, Farmington, CT, USA. cw739@cam.ac.uk.
Alexandra M NicaiseDepartment of Neuroscience, University of Connecticut School of Medicine, Farmington, CT, USA.ORCID http://orcid.org/0000-0001-7160-5988
Ernesto R BongarzoneDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Maria GivogriDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Cory R ReiterDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Olivia HeintzDepartment of Neuroscience, University of Connecticut School of Medicine, Farmington, CT, USA.
Evan R JellisonDepartment of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Pearl A SutterDepartment of Neuroscience, University of Connecticut School of Medicine, Farmington, CT, USA.
Gregg TeHennepeThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Guruprasad AnandaThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Anthony T VellaDepartment of Immunology, University of Connecticut School of Medicine, Farmington, CT, USA.
Stephen J CrockerDepartment of Neuroscience, University of Connecticut School of Medicine, Farmington, CT, USA. crocker@uchc.edu.ORCID http://orcid.org/0000-0003-4529-1385
University of Connecticut · USUniversity of Illinois Chicago · USJackson Laboratory · US

Funding

Proteomic and Functional Analyses of Astrocyte ExosomesR21NS087578 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CROCKER, STEPHEN J, VELLA, ANTHONY T · 2015 to 2016
$428k
NINDS NIH HHS R21 NS087578
6 · The paper itself

Abstract

The aging brain is associated with significant changes in physiology that alter the tissue microenvironment of the central nervous system (CNS). In the aged CNS, increased demyelination has been associated with astrocyte hypertrophy and aging has been implicated as a basis for these pathological changes. Aging tissues accumulate chronic cellular stress, which can lead to the development of a pro-inflammatory phenotype that can be associated with cellular senescence. Herein, we provide evidence that astrocytes aged in culture develop a spontaneous pro-inflammatory and senescence-like phenotype. We found that extracellular vesicles (EVs) from young astrocyte were sufficient to convey support for oligodendrocyte differentiation while this support was lost by EVs from aged astrocytes. Importantly, the negative influence of culture age on astrocytes, and their cognate EVs, could be countered by treatment with rapamycin. Comparative proteomic analysis of EVs from young and aged astrocytes revealed peptide repertoires unique to each age. Taken together, these findings provide new information on the contribution of EVs as potent mediators by which astrocytes can extert changing influence in either the disease or aged brain.

Indexed as

Cell DifferentiationCellular SenescenceAgingAnimalsAstrocytesBrainCells, CulturedExtracellular VesiclesMiceOligodendrogliaProteomics

Identifiers

PMID31964978
PMCPMC6972737
OpenAlexW3001162363

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.