Cited by 33Osteoarthritis Treatment and MechanismsProteoglycans and glycosaminoglycans researchPeriodontal Regeneration and Treatments

Anti-inflammatory Effect of DNA Polymeric Molecules in a Cell Model of Osteoarthritis

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Baek, Ahreum, Kim, MinGi, Kim, Sung Hoon, Cho, Sung-Rae, Kim, Hyun Jung·2018·Inflammation

Abstract

The DNA polymeric molecules polydeoxynucleotide (PDRN) and polynucleotide (PN) can be used as new alternative treatment for osteoarthritis (OA); however, the underlying mechanisms are not fully understood. In this study, we investigated the effect of PDRN and PN on gene-expression profiles in a cell model of OA using transcriptome analysis. Under hypoxic conditions, human chondrosarcoma cells were stressed for 24 h in the presence of interleukin (IL)-1β and subsequently treated with PDRN, PN, or hyaluronic acid (HA) for another 24 h, followed by transcriptome analysis. The results of the transcriptome study comprising differentially expressed genes were analyzed using the Database of Annotation Visualization and Integrated Discovery program, which yielded Kyoto Encyclopedia of Genes and Genomes pathways. Toll-like receptor (TLR)- and nucleotide-binding oligomerization domain-like receptor (NLR)-signaling pathways were related between the IL-1β group and the group treated with DNA polymeric molecules. The genes involved in the TLR- and NLR-signaling pathways were validated using real-time quantitative polymerase chain reaction and western blot. Among these genes, IL-6, IL-1β, IL-8, and chemokine (C-C motif) ligand 3 were dramatically upregulated in the IL-1β group, but significantly downregulated in the group treated with DNA polymeric molecules. Specifically, PN treatment resulted in a greater decrease in the expression of these genes as compared with PDRN treatment. Both PDR…

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Crossref · 10.1007/s10753-017-0722-2

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Authors
Baek, A., Kim, M., Kim, S. H., Cho, S.-R., & Kim, H. J.
Affiliations
  • Yonsei University (KR)
  • Eulji University (KR)
Corresponding author
  • Kim, Sung Hoon
  • Cho, Sung-Rae
  • Kim, Hyun Jung
Venue
Inflammation
Published
2018-01-04
Volume
41
Issue
2
Pages
677-688
ISSN
  • 0360-3997 (ISSN-L)
  • 1573-2576
OpenAlex
W2782458764
Cited by
33
References
3
Citations by year
2026: 4 · 2025: 7 · 2024: 7 · 2023: 3 · 2022: 4 · 2021: 3 · 2020: 1 · 2019: 1 · 2018: 3
FWCI
1.71
Type
journal article
Language
en
Open access
Locations
  • Inflammation (publishedVersion)
  • PubMed (publishedVersion)
  • YUHSpace (Yonsei University Medical Library) (submittedVersion, cc-by-nc-nd)
Funders
  • National Research Foundation (NRF-2014R1A2A1A11052042, NRF-2015M3A9B4067068, NRF-2017R1D1A1B03028855)
  • Ministry of Health & Welfare, Republic of Korea (HI16C1012)
  • Eulji University (KR) EMBRI (2015EMBRI SN0005)
Topics
  • Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
  • Health Sciences › Medicine › Urology › Periodontal Regeneration and Treatments
Keywords
osteoarthritis, polynucleotides, anti-inflammatory activity, IL-1β, hypoxia, chondrosarcoma cells, hyaluronic acid, Toll-like receptor signaling, NOD-like receptor signaling, gene expression profiling, interleukin-6, interleukin-8, cartilage inflammation
MeSH terms
Anti-Inflammatory Agents, Cells, Cultured, Chondrosarcoma, Humans, Osteoarthritis, Polydeoxyribonucleotides, Polynucleotides, Gene Expression Regulation, Neoplastic, Transcriptome

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