Evidence map›Paper›PMID 33708356›Full record

ArticleJournal of extracellular vesicles2020

An implanted device enables in vivo monitoring of extracellular vesicle-mediated spread of pro-inflammatory mast cell response in mice.

Krisztina V Vukman, Andrea Ferencz, Daniella Fehér, Krisztina Juhos, Péter Lőrincz, Tamás Visnovitz, Anna Koncz, Krisztina Pálóczi, Gábor Seregélyes, András Försönits and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  3. p16Immunity & ageing : I & A · 2024
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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

14 authors at 3 institutions in 1 country.

Krisztina V VukmanDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Andrea FerenczDepartment of Surgical Research and Techniques Semmelweis University Budapest Hungary.
Daniella FehérDepartment of Surgical Research and Techniques Semmelweis University Budapest Hungary.
Krisztina JuhosDepartment of Surgical Research and Techniques Semmelweis University Budapest Hungary.
Péter LőrinczDepartment of Anatomy Cell and Developmental Biology Eötvös Loránd University Budapest Hungary.
Tamás VisnovitzDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Anna KonczDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Krisztina PálócziDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Gábor SeregélyesDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
András FörsönitsDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Delaram KhamariDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
Alicia GalinsogaDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.
László DrahosMS Proteomics Research Group Hungarian Academy of Sciences Institute of Organic Chemistry Budapest Hungary.
Edit I BuzásDepartment of Genetics Cell- and Immunobiology Semmelweis University Budapest Hungary.ORCID 0000-0002-3744-206X
Semmelweis University · HUEötvös Loránd University · HUInstitute of Organic Chemistry · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mast cells have been shown to release extracellular vesicles (EVs) in vitro. However, EV-mediated mast cell communication in vivo remains unexplored. Primary mast cells from GFP-transgenic and wild type mice, were grown in the presence or absence of lipopolysaccharide (LPS), and the secreted EVs were separated from the conditioned media. Mast cell-derived EVs were next cultured with LPS-naïve mast cells, and the induction of TNF-α expression was monitored. In addition, primary mast cells were seeded in diffusion chambers that were implanted into the peritoneal cavities of mice. Diffusion chambers enabled the release of GFP

Indexed as

MAP Kinase Signaling SystemAnimalsCells, CulturedExtracellular VesiclesGene Expression RegulationInflammationLipopolysaccharidesMast CellsMiceMice, TransgenicTumor Necrosis Factor-alphaLipopolysaccharidesTumor Necrosis Factor-alphaextracellular vesiclesin vitroin vivoLPSmast cellTNF‐α

Identifiers

PMID33708356
PMCPMC7890545
OpenAlexW3119452690

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.