Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints From a Comparative Proteome Analysis
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Date
2021
Journal Title
Journal ISSN
Volume Title
Publisher
MDPI
Open Access Color
GOLD
Green Open Access
Yes
OpenAIRE Downloads
72
OpenAIRE Views
158
Publicly Funded
No
Abstract
Muse cells are adult stem cells that are present in the stroma of several organs and possess an enduring capacity to cope with endogenous and exogenous genotoxic stress. In cell therapy, the peculiar biological properties of Muse cells render them a possible natural alternative to mesenchymal stromal cells (MSCs) or to in vitro-generated pluripotent stem cells (iPSCs). Indeed, some studies have proved that Muse cells can survive in adverse microenvironments, such as those present in damaged/injured tissues. We performed an evaluation of Muse cells' proteome under basic conditions and followed oxidative stress treatment in order to identify ontologies, pathways, and networks that can be related to their enduring stress capacity. We executed the same analysis on iPSCs and MSCs, as a comparison. The Muse cells are enriched in several ontologies and pathways, such as endosomal vacuolar trafficking related to stress response, ubiquitin and proteasome degradation, and reactive oxygen scavenging. In Muse cells, the protein-protein interacting network has two key nodes with a high connectivity degree and betweenness: NFKB and CRKL. The protein NFKB is an almost-ubiquitous transcription factor related to many biological processes and can also have a role in protecting cells from apoptosis during exposure to a variety of stressors. CRKL is an adaptor protein and constitutes an integral part of the stress-activated protein kinase (SAPK) pathway. The identified pathways and networks are all involved in the quality control of cell components and may explain the stress resistance of Muse cells.
Description
Guner, Huseyin/0000-0002-0220-5224; Ozcan, Servet/0000-0002-9914-8843; Aprile, Domenico/0000-0003-1166-3259; Ayaz Guner, Serife/0000-0002-1052-0961; Acar, Mustafa Burak/0000-0002-9109-6575; Tez, Coskun/0000-0002-6816-7443; Di Bernardo, Giovanni/0000-0002-4985-4029;
Keywords
Stem Cells, DNA Damage, Oxidative Stress, Mesenchymal Stromal Cells, Proteomics, Proteome, Induced Pluripotent Stem Cells, DNA damage; Mesenchymal stromal cells; Oxidative stress; Stem cells; Adult Stem Cells; Cell Line; DNA Damage; Gene Ontology; Humans; Induced Pluripotent Stem Cells; Protein Interaction Maps; Proteome; Signal Transduction; Proteomics; Stress, Physiological, Article, Cell Line, Adult Stem Cells, Gene Ontology, stem cells, Stress, Physiological, DNA damage, oxidative stress, Humans, Protein Interaction Maps, mesenchymal stromal cells, DNA Damage, Signal Transduction
Fields of Science
0301 basic medicine, 03 medical and health sciences
Citation
WoS Q
Q1
Scopus Q
Q2

OpenCitations Citation Count
12
Source
International Journal of Molecular Sciences
Volume
22
Issue
4
Start Page
2064
End Page
PlumX Metrics
Citations
CrossRef : 12
Scopus : 13
PubMed : 11
Captures
Mendeley Readers : 14
SCOPUS™ Citations
13
checked on Mar 06, 2026
Web of Science™ Citations
13
checked on Mar 06, 2026
Page Views
8
checked on Mar 06, 2026
Downloads
3
checked on Mar 06, 2026
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