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Anti-inflammatory effects of polydeoxyribonucleotide and adipose tissue-derived mesenchymal stem cells in a canine cell model of osteoarthritis
被引:0
|作者:
Seo, Ju-Hui
[1
,2
]
Kim, Woo Keyoung
[1
,2
,3
]
Kang, Kyu-Won
[1
,2
]
Lee, Seoyun
[1
,2
,3
]
Kang, Byung-Jae
[1
,2
,3
]
机构:
[1] Seoul Natl Univ, Coll Vet Med, Dept Vet Clin Sci, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Vet Sci, 1 Gwanak Ro, Seoul 08826, South Korea
[3] Seoul Natl Univ, BK21 FOUR Future Vet Med Leading Educ & Res Ctr, Seoul 08826, South Korea
基金:
新加坡国家研究基金会;
关键词:
AdMSCs;
chondrocytes;
in vitro;
PDRN;
synoviocytes;
FIBROBLASTS;
MECHANISMS;
RECEPTORS;
SKIN;
D O I:
10.4142/jvs.24147
中图分类号:
S85 [动物医学(兽医学)];
学科分类号:
0906 ;
摘要:
Importance: A relatively new therapeutic agent for osteoarthritis (OA), polydeoxyribonucleotide (PDRN), shows potential in treating human OA due to its regenerative and anti-inflammatory effects. However, studies on PDRN for canine OA are limited, and no study has investigated their use with mesenchymal stem cells (MSCs) conventionally used for OA treatment. Objective: This study aimed to evaluate the potential of PDRN and explore its combined effect with adipose tissue-derived MSCs (AdMSCs) in treating canine OA. Methods: To study the impact of PDRN, canine chondrocytes, synoviocytes, and AdMSCs were exposed to various PDRN concentrations, and viability was assessed using cell counting kit-8. The OA model was created by treating chondrocytes and synoviocytes with lipopolysaccharide, followed by treatment under three different conditions: PDRN alone, AdMSCs alone, and a combination of PDRN and AdMSCs. Using real-time quantitative polymerase chain reaction, the anti-inflammatory effects and mechanisms were investigated by quantitatively assessing pro-inflammatory cytokines, collagen degradation markers, adenosine A2a receptor (ADORA2A), and nuclear factor-kappa B. Results: PDRN alone and combined with AdMSCs significantly reduced the expression of pro-inflammatory cytokines and collagen degradation markers in an OA model. PDRN promoted AdMSC proliferation and upregulated ADORA2A expression. AdMSCs exhibited comprehensive anti-inflammatory effects through paracrine effects, and both substances reduced inflammatory gene expression through different mechanisms, potentially enhancing therapeutic effects. Conclusions and Relevance: The results indicate that PDRN is a safe and effective antiinflammatory material that can be used independently or as an adjuvant for AdMSCs. Although additional research is necessary, this study is significant because it provides a foundation for future research at the cellular level.
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