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Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis

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 stroma...

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Autores principales: Acar, Mustafa B., Aprile, Domenico, Ayaz-Guner, Serife, Guner, Huseyin, Tez, Coskun, Di Bernardo, Giovanni, Peluso, Gianfranco, Ozcan, Servet, Galderisi, Umberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922977/
https://www.ncbi.nlm.nih.gov/pubmed/33669748
http://dx.doi.org/10.3390/ijms22042064
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author Acar, Mustafa B.
Aprile, Domenico
Ayaz-Guner, Serife
Guner, Huseyin
Tez, Coskun
Di Bernardo, Giovanni
Peluso, Gianfranco
Ozcan, Servet
Galderisi, Umberto
author_facet Acar, Mustafa B.
Aprile, Domenico
Ayaz-Guner, Serife
Guner, Huseyin
Tez, Coskun
Di Bernardo, Giovanni
Peluso, Gianfranco
Ozcan, Servet
Galderisi, Umberto
author_sort Acar, Mustafa B.
collection PubMed
description 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.
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spelling pubmed-79229772021-03-03 Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis Acar, Mustafa B. Aprile, Domenico Ayaz-Guner, Serife Guner, Huseyin Tez, Coskun Di Bernardo, Giovanni Peluso, Gianfranco Ozcan, Servet Galderisi, Umberto Int J Mol Sci Article 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. MDPI 2021-02-19 /pmc/articles/PMC7922977/ /pubmed/33669748 http://dx.doi.org/10.3390/ijms22042064 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Acar, Mustafa B.
Aprile, Domenico
Ayaz-Guner, Serife
Guner, Huseyin
Tez, Coskun
Di Bernardo, Giovanni
Peluso, Gianfranco
Ozcan, Servet
Galderisi, Umberto
Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title_full Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title_fullStr Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title_full_unstemmed Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title_short Why Do Muse Stem Cells Present an Enduring Stress Capacity? Hints from a Comparative Proteome Analysis
title_sort why do muse stem cells present an enduring stress capacity? hints from a comparative proteome analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922977/
https://www.ncbi.nlm.nih.gov/pubmed/33669748
http://dx.doi.org/10.3390/ijms22042064
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