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Differential expression of lncRNAs and mRNAs in bone marrow-derived mesenchymal stem cells under continuous and intermittent teriparatide treatment
ID Vrščaj, Lucija Ana (Avtor), ID Marc, Janja (Avtor), ID Ostanek, Barbara (Avtor)

URLURL - Izvorni URL, za dostop obiščite https://www.sciencedirect.com/science/article/pii/S0753332225004871?via%3Dihub Povezava se odpre v novem oknu
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MD5: 0D1628BB172B28E367925030F919F71B
URLURL - Izvorni URL, za dostop obiščite https://www.sciencedirect.com/science/article/pii/S0753332225004871 Povezava se odpre v novem oknu

Izvleček
A deeper understanding of how teriparatide exerts its anabolic effects on bone tissue may open new avenues for osteoanabolic treatment. Our study aimed to identify long non-coding RNAs and messenger RNAs (mRNAs) regulated by teriparatide. Bone marrow mesenchymal stem cells (MSCs) were treated with teriparatide during osteogenic differentiation, and long RNA sequencing was performed. We identified 7 622 differentially expressed lncRNAs in both continuous and intermittent treatment groups compared to untreated MSCs. In intermittent treatment, the most upregulated lncRNAs were VCP, EMP1, OXA1L, LPP, and SCARB2, while in continuous treatment, they were XLOC_055533, SCARB2, HNRNPC, VCP, and CALM3. The most downregulated lncRNAs in intermittent treatment were KRTAP4–11, DUBR, MEG3, DIABLO, and ABI3BP, while in continuous treatment, they were XLOC_055164, SLC2A3, COPG1, and SMTN. Among mRNAs, the most upregulated in intermittent treatment were DNAJC25-GNG10, ZBTB4, SLC2A6, TMEM189-UBE2V1, and BDP1, whereas SLC2A6, ZBTB4, MX1, BDP1, and RSAD2 were the most upregulated in continuous treatment. The most downregulated mRNAs in intermittent treatment were PIP4K2B, GFI1B, ISY1-RAB43, AC010422.5, SESN2 and ISY1-RAB43, whereas ZDBF2, KLKB1, RPS10-NUDT3, and XLOC_055092 were the most downregulated mRNAs in continuous treatment. AC008622.2, MED17, and RNF213 emerged as the most critical lncRNAs for elucidating the mechanism of intermittent teriparatide therapy, while XLOC_055533, SPG7, and HOOK3 were highlighted as the most important lncRNAs in the continuous treatment. Additionally, we identified novel lncRNAs (KRTAP4–11, CEBPZOS, and CDC42SE2) that may have a role in teriparatide effects on MSCs. Identified lncRNAs and mRNAs could serve as therapeutic targets or diagnostic markers to improve osteoanabolic treatments.

Jezik:Angleški jezik
Ključne besede:teriparatide, lncRNAs, mRNAs, bone marrow mesenchymal stem cells (bMSCs), osteogenic differentiation, differential expression
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FFA - Fakulteta za farmacijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:11 str.
Številčenje:Vol. 189, art. no. 118293
PID:20.500.12556/RUL-177227 Povezava se odpre v novem oknu
UDK:616-097:616.71-007.234
ISSN pri članku:1950-6007
DOI:10.1016/j.biopha.2025.118293 Povezava se odpre v novem oknu
COBISS.SI-ID:259941123 Povezava se odpre v novem oknu
Datum objave v RUL:18.12.2025
Število ogledov:357
Število prenosov:324
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Biomedicine & pharmacotherapy
Skrajšan naslov:Biomed. pharmacother.
Založnik:Éditions scientifiques et médicales Elsevier
ISSN:1950-6007
COBISS.SI-ID:23136261 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC 4.0, Creative Commons Priznanje avtorstva-Nekomercialno 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc/4.0/deed.sl
Opis:Licenca Creative Commons, ki prepoveduje komercialno uporabo, vendar uporabniki ne rabijo upravljati materialnih avtorskih pravic na izpeljanih delih z enako licenco.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:teriparatid, lncRNA, mRNA, mezenhimske matične celice kostnega mozga (bMSC), osteogena diferenciacija, diferencialna ekspresija

Projekti

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0298-2019
Naslov:Geni, hormonske in osebnostne spremembe pri metabolnih motnjah

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:J3-1759-2019
Naslov:Celostna karakterizacija zadetkov analiz GWAS - pot do novih terapevtskih tarč za anabolno zdravljenje osteoporoze(GWASforAna)

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:J3-4527-2022
Naslov:Mišični sekretom in kostne celice - sodelovanje pri osteosarkopeniji (MiKOSA)

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