Publication: Improving stemness and functional features of mesenchymal stem cells from Wharton's jelly of a human umbilical cord by mimicking the native, low oxygen stem cell niche
| dc.contributor.author | Obradovic, Hristina (56444469700) | |
| dc.contributor.author | Krstic, Jelena (26532883400) | |
| dc.contributor.author | Trivanovic, Drenka (54421475000) | |
| dc.contributor.author | Mojsilovic, Slavko (14036036900) | |
| dc.contributor.author | Okic, Ivana (55749320000) | |
| dc.contributor.author | Kukolj, Tamara (56001838100) | |
| dc.contributor.author | Ilic, Vesna (57190793777) | |
| dc.contributor.author | Jaukovic, Aleksandra (7006010128) | |
| dc.contributor.author | Terzic, Milan (55519713300) | |
| dc.contributor.author | Bugarski, Diana (35616659100) | |
| dc.date.accessioned | 2025-07-02T12:10:29Z | |
| dc.date.available | 2025-07-02T12:10:29Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Introduction: Mesenchymal stem cells from Wharton's Jelly of a human umbilical cord (WJ-MSCs) are a potential tool in regenerative medicine based on their availability, proliferative potential and differentiation capacity. Since their physiological niche contains low oxygen levels, we investigated whether cultivation of WJ-MSCs at 3% O2 affects their main features. Methods: WJ-MSCs were cultured under 21% and 3% O2. Proliferation rate was followed by short and long term proliferation assays, clonogenic capacity by CFU-F assay and cell cycle and death by flow cytometry. Differentiation capacity was investigated by histochemical staining after induced differentiation. Pluripotency and differentiation markers' expression was determined by RT-PCR. Migration capacity was followed by scratch assay and mobilization from collagen, and the activity of proteolytic enzymes by zymography. Specific inhibitors of MAPK and Wnt/β-catenin pathways were used to investigate underlying molecular mechanisms. Results: Compared to standard 21% O2, cultivation of WJ-MSCs at 3% O2 did not influence their immunophenotype, while it modulated their differentiation process and enhanced their clonogenic and expansion capacity. 3% O2 induced transient change in cell cycle and prevented cell death. The expression of NANOG, OCT4A, OCT4B and SOX2 was increased at 3% O2. Both cultivation and preculturing of WJ-MSCs at 3% O2 increased their in vitro migratory capacity and enhanced the activity of proteolytic enzymes. ERK1/2 mediated WJ-MSCs’ mobilization from collagen regardless of oxygen levels, while Wnt/β-catenin pathway was activated during migration and mobilization at standard conditions. Conclusion: Culturing of WJ-MSCs under 3% O2 should be considered a credible condition when investigating their properties and potential use. © 2019 Elsevier Ltd | |
| dc.identifier.uri | https://doi.org/10.1016/j.placenta.2019.05.005 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85065744920&doi=10.1016%2fj.placenta.2019.05.005&partnerID=40&md5=f2d236914a7b58180d00b3939496552f | |
| dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/12727 | |
| dc.subject | Hypoxia | |
| dc.subject | Mesenchymal stem cells (MSC) | |
| dc.subject | Migration | |
| dc.subject | Stemness | |
| dc.subject | Wharton's jelly | |
| dc.title | Improving stemness and functional features of mesenchymal stem cells from Wharton's jelly of a human umbilical cord by mimicking the native, low oxygen stem cell niche | |
| dspace.entity.type | Publication |
