Literature DB >> 33669748

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

Mustafa B Acar1,2, Domenico Aprile3, Serife Ayaz-Guner4, Huseyin Guner4, Coskun Tez2,5, Giovanni Di Bernardo3,6, Gianfranco Peluso7, Servet Ozcan2,5, Umberto Galderisi2,3,6.   

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.

Entities:  

Keywords:  DNA damage; mesenchymal stromal cells; oxidative stress; stem cells

Mesh:

Substances:

Year:  2021        PMID: 33669748      PMCID: PMC7922977          DOI: 10.3390/ijms22042064

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  36 in total

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Authors:  Alexandra Vaisman; John P McDonald; Roger Woodgate
Journal:  EcoSal Plus       Date:  2012-11

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6.  Protocol Update for large-scale genome and gene function analysis with the PANTHER classification system (v.14.0).

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7.  Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis.

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8.  InnateDB: systems biology of innate immunity and beyond--recent updates and continuing curation.

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Journal:  Nucleic Acids Res       Date:  2012-11-24       Impact factor: 16.971

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  3 in total

1.  Inhibition of Gap Junctional Intercellular Communication Upregulates Pluripotency Gene Expression in Endogenous Pluripotent Muse Cells.

Authors:  Khaled Hatabi; Yukari Hirohara; Yoshihiro Kushida; Yasumasa Kuroda; Shohei Wakao; James Trosko; Mari Dezawa
Journal:  Cells       Date:  2022-08-30       Impact factor: 7.666

2.  Naïve pluripotent-like characteristics of non-tumorigenic Muse cells isolated from human amniotic membrane.

Authors:  Eiji Ogawa; Yo Oguma; Yoshihiro Kushida; Shohei Wakao; Kana Okawa; Mari Dezawa
Journal:  Sci Rep       Date:  2022-10-14       Impact factor: 4.996

3.  Molecular Morphology and Function of Stromal Cells.

Authors:  Mirko Manetti
Journal:  Int J Mol Sci       Date:  2021-12-14       Impact factor: 5.923

  3 in total

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