Evidence map›Paper›PMID 38069411›Full record

ArticleInternational journal of molecular sciences2023

M2-Macrophage-Induced Chronic Inflammation Promotes Reversible Mesenchymal Stromal Cell Senescence and Reduces Their Anti-Fibrotic Properties.

Uliana Dyachkova, Maksim Vigovskiy, Nataliya Basalova, Anastasia Efimenko, Olga Grigorieva

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 14 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

5 authors at 1 institution in 1 country.

Uliana DyachkovaFaculty of Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia.
Maksim VigovskiyFaculty of Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0003-2103-8158
Nataliya BasalovaFaculty of Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia.
Anastasia EfimenkoFaculty of Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0002-0696-1369
Olga GrigorievaFaculty of Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia.
Lomonosov Moscow State University · RU

Funding

Russian Science Foundation 19-75-30007
6 · The paper itself

Abstract

Fibrosis and the associated decline in organ functionality lead to an almost 50% mortality rate in developed countries. Multipotent mesenchymal stromal cells (MSC) were shown to suppress the development and progression of fibrosis through secreted factors including specific non-coding RNAs transferred within extracellular vesicles (EV). However, age-associated chronic inflammation can provoke MSC senescence and change secretome composition, thereby affecting their antifibrotic properties. Alternatively activated macrophages (M2-type) are key players in chronic inflammation that may interact with MSC through paracrine mechanisms and decrease their antifibrotic functions. To confirm this hypothesis, we evaluated the M2-macrophage conditioned medium (CM-M2) effect on human adipose-tissue-derived MSC senescence in vitro. We found that CM-M2, as well as a pro-senescence agent, hydrogen peroxide (H

Indexed as

Cellular SenescenceMesenchymal Stem CellsFibrosisHumansHydrogen PeroxideInflammationMacrophagesHydrogen Peroxidechronic inflammationextracellular vesiclesfibroblast-to-myofibroblast differentiationfibrosismacrophagesmultipotent mesenchymal stromal cells

Identifiers

PMID38069411
PMCPMC10707628
OpenAlexW4389311406

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.