Evidence map›Paper›PMID 33659050›Full record

ArticleJournal of extracellular vesicles2021

Isolation methodology is essential to the evaluation of the extracellular vesicle component of the senescence-associated secretory phenotype.

Ryan Wallis, Natasa Josipovic, Hannah Mizen, Arturo Robles-Tenorio, Eleanor J Tyler, Argyris Papantonis, Cleo L Bishop

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Ryan WallisBlizard Institute of Cell and Molecular Science Barts and The London School of Medicine and Dentistry London UK.
Natasa JosipovicInstitute of Pathology University Medical Centre Göttingen Göttingen Germany.
Hannah MizenBlizard Institute of Cell and Molecular Science Barts and The London School of Medicine and Dentistry London UK.
Arturo Robles-TenorioBlizard Institute of Cell and Molecular Science Barts and The London School of Medicine and Dentistry London UK.
Eleanor J TylerBlizard Institute of Cell and Molecular Science Barts and The London School of Medicine and Dentistry London UK.
Argyris PapantonisInstitute of Pathology University Medical Centre Göttingen Göttingen Germany.
Cleo L BishopBlizard Institute of Cell and Molecular Science Barts and The London School of Medicine and Dentistry London UK.
Queen Mary University of London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M009513/1Medical Research Council MR/K501372/1
6 · The paper itself

Abstract

A hallmark of senescence is the acquisition of an enhanced secretome comprising inflammatory mediators and tissue remodelling agents - the senescence-associated secretory phenotype (SASP). Through the SASP, senescent cells are hypothesised to contribute to both ageing and pathologies associated with age. Whilst soluble factors have been the most widely investigated components of the SASP, there is growing evidence that small extracellular vesicles (EVs) comprise functionally important constituents. Thus, dissecting the contribution of the soluble SASP from the vesicular component is crucial to elucidating the functional significance of senescent cell derived EVs. Here, we take advantage of a systematic proteomics based approach to determine that soluble SASP factors co-isolate with EVs following differential ultracentrifugation (dUC). We present size-exclusion chromatography (SEC) as a method for separation of the soluble and vesicular components of the senescent secretome and thus EV purification. Furthermore, we demonstrate that SEC EVs isolated from senescent cells contribute to non-cell autonomous paracrine senescence. Therefore, this work emphasises the requirement for methodological rigor due to the propensity of SASP components to co-isolate during dUC and provides a framework for future investigations of the vesicular component of the SASP.

Indexed as

Cellular SenescenceSenescence-Associated Secretory PhenotypeAgingCell Line, TumorCells, CulturedChromatography, GelExosomesExtracellular VesiclesHumansPhenotypeProteinsProteomicsSecretomeProteinsageingexosomesextracellular vesiclesparacrine senescencesenescencesenescence‐associated secretory phenotype

Identifiers

PMID33659050
PMCPMC7892802
OpenAlexW3130240542

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.