Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Repository of the University of Ljubljana
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Advanced
New in RUL
About RUL
In numbers
Help
Sign in
Details
Differential expression of lncRNAs and mRNAs in bone marrow-derived mesenchymal stem cells under continuous and intermittent teriparatide treatment
ID
Vrščaj, Lucija Ana
(
Author
),
ID
Marc, Janja
(
Author
),
ID
Ostanek, Barbara
(
Author
)
URL - Source URL, Visit
https://www.sciencedirect.com/science/article/pii/S0753332225004871?via%3Dihub
PDF - Presentation file,
Download
(2,15 MB)
MD5: 0D1628BB172B28E367925030F919F71B
URL - Source URL, Visit
https://www.sciencedirect.com/science/article/pii/S0753332225004871
Image galllery
Abstract
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.
Language:
English
Keywords:
teriparatide
,
lncRNAs
,
mRNAs
,
bone marrow mesenchymal stem cells (bMSCs)
,
osteogenic differentiation
,
differential expression
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2025
Number of pages:
11 str.
Numbering:
Vol. 189, art. no. 118293
PID:
20.500.12556/RUL-177227
UDC:
616-097:616.71-007.234
ISSN on article:
1950-6007
DOI:
10.1016/j.biopha.2025.118293
COBISS.SI-ID:
259941123
Publication date in RUL:
18.12.2025
Views:
390
Downloads:
348
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Biomedicine & pharmacotherapy
Shortened title:
Biomed. pharmacother.
Publisher:
Éditions scientifiques et médicales Elsevier
ISSN:
1950-6007
COBISS.SI-ID:
23136261
Licences
License:
CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:
http://creativecommons.org/licenses/by-nc/4.0/
Description:
A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.
Secondary language
Language:
Slovenian
Keywords:
teriparatid
,
lncRNA
,
mRNA
,
mezenhimske matične celice kostnega mozga (bMSC)
,
osteogena diferenciacija
,
diferencialna ekspresija
Projects
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P3-0298-2019
Name:
Geni, hormonske in osebnostne spremembe pri metabolnih motnjah
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J3-1759-2019
Name:
Celostna karakterizacija zadetkov analiz GWAS - pot do novih terapevtskih tarč za anabolno zdravljenje osteoporoze(GWASforAna)
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J3-4527-2022
Name:
Mišični sekretom in kostne celice - sodelovanje pri osteosarkopeniji (MiKOSA)
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back