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Comprehensive analysis of skeletal muscle- and bone-derived mesenchymal stem/stromal cells in patients with osteoarthritis and femoral neck fracture
ID
Čamernik, Klemen
(
Author
),
ID
Mihelič, Anže
(
Author
),
ID
Mihalič, Rene
(
Author
),
ID
Haring, Gregor
(
Author
),
ID
Herman, Simon
(
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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https://stemcellres.biomedcentral.com/articles/10.1186/s13287-020-01657-z
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Abstract
Background: Mesenchymal stem/stromal cells (MSCs) can replenish the aged cells of the musculoskeletal system in adult life. Stem cell exhaustion and decrease in their regenerative potential have been suggested to be hallmarks of aging. Here, we investigated whether muscle- and bone-derived MSCs of patients with osteoarthritis and osteoporosis are affected by this exhaustion, compared to healthy donors. Methods: Patients with primary osteoarthritis, femoral neck fractures due to osteoporosis, and healthy donors (controls) were included. MSCs were isolated from the skeletal muscle and subchondral bone from each patient and compared using ex vivo and in vitro analyses, including immunophenotyping, colony-forming unit fibroblast assays, growth kinetics, cell senescence, multilineage potential, and MSC marker gene expression profiling. Results: Freshly isolated cells from muscle from patients with osteoarthritis showed a lower proportion of CD45/CD19/CD14/CD34-negative cells compared to patients with osteoporosis and healthy donors. Freshly isolated muscle cells from patients with osteoarthritis and osteoporosis also showed higher clonogenicity compared to healthy donors. MSCs from both tissues of osteoarthritis patients showed significantly reduced osteogenesis and MSCs from the bone also reduced adipogenesis. Chondrogenic pellet diameter was reduced in bone-derived MSCs from both patient groups compared to healthy donors. A significant positive correlation was observed between adipogenesis and CD271 expression in muscle-derived MSCs. CD73 was significantly lower in bone-derived MSCs from osteoarthritis patients, compared to osteoporosis patients. Gene expression profiling showed significantly lower expression of MSC marker gene leptin receptor, LEPR, previously identified as the major source of the bone and adipocytes in the adult bone marrow, in bone-derived MSCs from patients with osteoarthritis in comparison with osteoporotic patients and healthy donors. Conclusions: Our results show deficient ex vivo and in vitro properties of both skeletal muscle- and bone-derived MSCs in osteoarthritis and osteoporosis patients, compared to healthy donors. In bone-derived MSCs from patients with osteoarthritis, we also identified a lower expression of the leptin receptor, a marker of MSCs that present a major source of MSCs in the adult bone marrow. This suggests that exhaustion of skeletal muscle- and bone-derived MSCs is a hallmark of osteoarthritis and osteoporosis, which defines the need for further clinical trials of stem cell transplantation in these patients.
Language:
English
Keywords:
mesenchymal stem/stromal cells
,
skeletal muscle
,
trabecular bone
,
osteoarthritis
,
osteoporosis
,
controls
,
leptin receptor
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2020
Number of pages:
14 str.
Numbering:
Vol. 11, iss. 1, art. 146
PID:
20.500.12556/RUL-125371
UDC:
616.4
ISSN on article:
1757-6512
DOI:
10.1186/s13287-020-01657-z
COBISS.SI-ID:
34763993
Publication date in RUL:
12.03.2021
Views:
1186
Downloads:
309
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Record is a part of a journal
Title:
Stem cell research & therapy
Publisher:
Springer Nature
ISSN:
1757-6512
COBISS.SI-ID:
27049945
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
12.03.2021
Secondary language
Language:
Slovenian
Keywords:
osteoartritis
,
mezenhimalne/stromalne matične celice
,
celovita analiza
,
osteoporoza. leptinski receptor
,
kontrola
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:
ARRS - Slovenian Research Agency
Project number:
J3-1749
Name:
Mezenhimske matične celice-nosilci endogene regenerativne sposobnosti tkiv v boju proti staranju mišično-skeletnega sistema
Funder:
EC - European Commission
Funding programme:
Interreg Italia-Slovenia 2014–2020
Acronym:
ARTE
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