Evidence map›Paper›PMID 32727501›Full record

ArticleCell communication and signaling : CCS2020

A comparative study on normal and obese mice indicates that the secretome of mesenchymal stromal cells is influenced by tissue environment and physiopathological conditions.

Serife Ayaz-Guner, Nicola Alessio, Mustafa B Acar, Domenico Aprile, Servet Özcan, Giovanni Di Bernardo, Gianfranco Peluso, Umberto Galderisi

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cell communication and signaling : CCS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  17. Translating MSC Therapy in the Age of Obesity.Frontiers in immunology · 2022
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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

8 authors at 5 institutions in 3 countries.

Serife Ayaz-GunerDepartment of Molecular Biology and Genetics, Faculty of Life and Natural Science, Abdullah Gül University, Kayseri, Turkey.
Nicola AlessioDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Mustafa B AcarGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Turkey.
Domenico AprileDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Servet ÖzcanGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Turkey.
Giovanni Di BernardoDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Gianfranco PelusoResearch Institute on Ecosystems (IRET); CNR, Naples, Italy.
Umberto GalderisiDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy. umberto.galderisi@unicampania.it.ORCID 0000-0003-0909-7403
University of Campania "Luigi Vanvitelli" · ITErciyes University · TRAbdullah Gül University · TRInstitute of Ecosystem Study · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe term mesenchymal stromal cells (MSCs) designates an assorted cell population comprised of stem cells, progenitor cells, fibroblasts, and stromal cells. MSCs contribute to the homeostatic maintenance of many organs through paracrine and long-distance signaling. Tissue environment, in both physiological and pathological conditions, may affect the intercellular communication of MSCs.

methodsWe performed a secretome analysis of MSCs isolated from subcutaneous adipose tissue (sWAT) and visceral adipose tissue (vWAT), and from bone marrow (BM), of normal and obese mice.

resultsThe MSCs isolated from tissues of healthy mice share a common core of released factors: components of cytoskeletal and extracellular structures; regulators of basic cellular functions, such as protein synthesis and degradation; modulators of endoplasmic reticulum stress; and counteracting oxidative stress. It can be hypothesized that MSC secretome beneficially affects target cells by the horizontal transfer of many released factors. Each type of MSC may exert specific signaling functions, which could be determined by looking at the many factors that are exclusively released from every MSC type. The vWAT-MSCs release factors that play a role in detoxification activity in response to toxic substances and drugs. The sWAT-MSC secretome contains proteins involved in in chondrogenesis, osteogenesis, and angiogenesis. Analysis of BM-MSC secretome revealed that these cells exert a signaling function by remodeling extracellular matrix structures, such as those containing glycosaminoglycans. Obesity status profoundly modified the secretome content of MSCs, impairing the above-described activity and promoting the release of inflammatory factors.

conclusionWe demonstrated that the content of MSC secretomes depends on tissue microenvironment and that pathological condition may profoundly alter its composition. Video abstract.

Indexed as

Organ SpecificityAnimalsAntigensBlood PlateletsCell DegranulationDiet, High-FatGene OntologyMaleMesenchymal Stem CellsMice, Inbred C57BLMice, ObeseModels, BiologicalSolubilityAntigensMesenchymal stromal cellsObesitySecretome

Identifiers

PMID32727501
PMCPMC7388533
OpenAlexW3045985956

What OpenQuestion holds

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LicenceCC BY
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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.