Therapeutic Effects of PEG-Modified Polyamide Amine Dendrimer for Cell Free DNA Adsorption in Temporomandibular Joint Osteoarthritis.
Yuzhuo HeiJingyi DuZhizhao DengYifan DengYu GuanJing YangSufang ChenZiyi ZhangSiqing JiangQingbin ZhangPublished in: ACS applied materials & interfaces (2024)
Temporomandibular joint osteoarthritis (TMJ OA) is characterized by the degeneration of cartilage and subchondral bone. In this study, we observed a significant increase in cell-free DNA (cfDNA) levels during the progression of TMJ OA. Bioinformatics analysis identified TLR9 as a pivotal molecule in TMJ OA pathogenesis. The polyamidoamine (PAMAM) dendrimer characterized by a well-structured, highly branched, and reactive nature, exhibits robust binding and clearance capabilities for cfDNA. However, the abundant amino groups on the surface of PAMAM lead to its inherent toxicity. To mitigate this, PEG-5000 was conjugated to the surface of PAMAM dendrimers, enhancing safety. Our results indicate that PEG-PAMAM effectively inhibits the upregulation of the TLR9 protein in TMJ OA, significantly suppressing the activation of the p-IκBα/p-NF-κB signaling pathway and subsequently decreasing chondrocyte inflammation and apoptosis, as evidenced by both in vivo and in vitro experiments. We conclude that PEG-PAMAM is a safe and effective material for in vivo applications, offering a promising therapeutic strategy for TMJ OA by targeting cfDNA clearance.
Keyphrases
- knee osteoarthritis
- signaling pathway
- oxidative stress
- drug delivery
- pi k akt
- toll like receptor
- inflammatory response
- bioinformatics analysis
- immune response
- rheumatoid arthritis
- induced apoptosis
- cell cycle arrest
- nuclear factor
- epithelial mesenchymal transition
- cell proliferation
- cell death
- lps induced
- extracellular matrix
- protein protein
- long non coding rna