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Skeletal-muscle-derived mesenchymal stem/stromal cells from patients with osteoarthritis show superior biological properties compared to bone-derived cells
ID Čamernik, Klemen (Author), ID Mihelič, Anže (Author), ID Mihalič, Rene (Author), ID Marolt, Darja (Author), ID Janež, Andrej (Author), ID Trebše, Rihard (Author), ID Marc, Janja (Author), ID Zupan, Janja (Author)

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Abstract
Mesenchymal stem/stromal cells (MSCs) are being exploited for patient-derived stem-cell therapies. As the biological properties of MSCs derived from skeletal muscle of osteoarthritis patients are poorly understood, the aim of this study was to compare muscle MSCs with well-recognized bone and bone marrow-derived MSCs from these patients. Paired samples of skeletal muscle and trabecular bone tissue were obtained from 21 patients with osteoarthritis. Isolated cells were compared using ex vivo immunophenotyping and detailed in vitro analyses. These included the colony forming unit fibroblast assay, growth kinetics, senescence, multilineage potential, immunophenotyping, and MSC marker gene expression profiling. Freshly isolated MSCs from muscle showed improved viability over bone-derived MSCs, with similar mesenchymal fraction. Muscle-derived MSCs showed superior clonogenicity, higher growth rates, and lower doubling times. Muscle-derived MSCs also showed superior osteogenic and myogenic properties and a positive correlation between CD271 expression and adipogenesis. Senescence rate as well as adipogenic and chondrogenic potentials were similar. Skeletal muscle-derived MSCs of osteoarthritis patients have superior clonogenicity and growth kinetics compared to bone-derived MSCs, making them a good candidate for autologous stem-cell therapies. Moreover, the positive correlation between CD271 and adipogenesis suggest that CD271 expressing muscle MSCs might contribute to muscle steatosis observed in osteoarthritis.

Language:English
Keywords:mesenchymal stem/stromal cells, osteoarthritis, bone, muscle, CD271
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2019
Number of pages:12 str.
Numbering:Vol. 38, art. 101465
PID:20.500.12556/RUL-137727 This link opens in a new window
UDC:576.3:616.71-007.234
ISSN on article:1873-5061
DOI:10.1016/j.scr.2019.101465 This link opens in a new window
COBISS.SI-ID:4717937 This link opens in a new window
Publication date in RUL:29.06.2022
Views:457
Downloads:89
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Record is a part of a journal

Title:Stem cell research
Publisher:Elsevier
ISSN:1873-5061
COBISS.SI-ID:519732761 This link opens in a new window

Licences

License:CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.

Secondary language

Language:Slovenian
Keywords:artroza, matične celice

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P3-0298
Name:Geni, hormonske in osebnostne spremembe pri metabolnih motnjah

Funder:ARRS - Slovenian Research Agency
Project number:J3-7245
Name:Odkrivanje novih regulatorjev izražanja RANKL, ključne molekule ne samo v kostni prenovi

Funder:EC - European Commission
Funding programme:Interreg Italia Slovenia
Acronym:ARTE

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