Evidence map›Paper›PMID 27463232›Full record

ArticleCell cycle (Georgetown, Tex.)2017

The secretome of MUSE cells contains factors that may play a role in regulation of stemness, apoptosis and immunomodulation.

Nicola Alessio, Servet Özcan, Kazuki Tatsumi, Ayşegül Murat, Gianfranco Peluso, Mari Dezawa, Umberto Galderisi

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.4field-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

46 citing papers in PubMed, 73 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 4 countries.

Nicola Alessioa Department of Experimental Medicine , Biotechnology and Molecular Biology Section, Second University of Naples , Naples , Italy.
Servet Özcanb Genome and Stem Cell Center (GENKOK), Erciyes University , Kayseri , Turkey.
Kazuki Tatsumid Department of Stem Cell Biology and Histology , Tohoku University Graduate School of Medicine , Sendai , Japan.
Ayşegül Muratc Graduate School of Health Sciences, Erciyes Universty , Kayseri , Turkey.
Gianfranco Pelusof Institute of Bioscience and Bioresources, CNR , Naples , Italy.
Mari Dezawae Tohoku Laboratory Non-clinical Research Division, Clio, Inc. , Sendai , Japan.
Umberto Galderisia Department of Experimental Medicine , Biotechnology and Molecular Biology Section, Second University of Naples , Naples , Italy.
Erciyes University · TRInstitute of Biosciences and Bioresources · ITTohoku University · JPUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) are a heterogeneous population, which contain several cell phenotypes: mesenchymal stem cells, progenitor cells, fibroblasts and other type of cells. Previously, we identified unique stem cells that we named multilineage-differentiating stress enduring (Muse) cells as one to several percent of MSCs of the bone marrow, adipose tissue and dermis. Among different cell populations in MSCs, Muse cells, positive for pluripotent surface marker SSEA-3, may represent cells responsible for pluripotent-like property of MSCs, since they express pluripotency genes, able to differentiated into triploblastic cells from a single cells and are self-renewable. MSCs release biologically active factors that have profound effects on local cellular dynamics. A thorough examination of MSC secretome seems essential for understanding the physiological functions exerted by these cells in our organism and also for rational cellular therapy design. In this setting, studies on secretome of Muse cells may shed light on pathways that are associated with their specific features. Our findings evidenced that secretomes of MSCs and Muse cells contain factors that regulate extracellular matrix remodeling, ox-redox activities and immune system. Muse cells appear to secrete factors that may preserve their stem cell features, allow survival under stress conditions and may contribute to their immunomodulation capacity. In detail, the proteins belonging to protein kinase A signaling, FXR/RXR activation and LXR/RXR activation pathways may play a role in regulation of Muse stem cell features. These last 2 pathways together with proteins associated with antigen presentation pathway and coagulation system may play a role in immunomodulation.

Indexed as

ApoptosisCell DifferentiationCell LineageImmunomodulationMetabolomeStress, PhysiologicalCells, CulturedGene OntologyGene Regulatory NetworksHumansMesenchymal Stem CellsSignal TransductionapoptosiscancerMesenchymal stem cellssecretomesenescence

Identifiers

PMID27463232
PMCPMC5270533
OpenAlexW2501096092

What OpenQuestion holds

Textmetadata
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.