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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 (Avtor), ID Mihelič, Anže (Avtor), ID Mihalič, Rene (Avtor), ID Marolt, Darja (Avtor), ID Janež, Andrej (Avtor), ID Trebše, Rihard (Avtor), ID Marc, Janja (Avtor), ID Zupan, Janja (Avtor)

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Izvleček
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.

Jezik:Angleški jezik
Ključne besede:mesenchymal stem/stromal cells, osteoarthritis, bone, muscle, CD271
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FFA - Fakulteta za farmacijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2019
Št. strani:12 str.
Številčenje:Vol. 38, art. 101465
PID:20.500.12556/RUL-137727 Povezava se odpre v novem oknu
UDK:576.3:616.71-007.234
ISSN pri članku:1873-5061
DOI:10.1016/j.scr.2019.101465 Povezava se odpre v novem oknu
COBISS.SI-ID:4717937 Povezava se odpre v novem oknu
Datum objave v RUL:29.06.2022
Število ogledov:869
Število prenosov:110
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Stem cell research
Založnik:Elsevier
ISSN:1873-5061
COBISS.SI-ID:519732761 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:artroza, matične celice

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0298
Naslov:Geni, hormonske in osebnostne spremembe pri metabolnih motnjah

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:J3-7245
Naslov:Odkrivanje novih regulatorjev izražanja RANKL, ključne molekule ne samo v kostni prenovi

Financer:EC - European Commission
Program financ.:Interreg Italia Slovenia
Akronim:ARTE

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