Quercetin-Loaded Bioglass Injectable Hydrogel Promotes m6A Alteration of Per1 to Alleviate Oxidative Stress for Periodontal Bone Defects.
Huimin ZhuChao CaiYeke YuYuning ZhouShiyuan YangYue HuYan ZhuJia ZhouJieyun ZhaoHailong MaYujie ChenYuanjin XuPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Periodontal disease ranks third among noncommunicable illnesses, behind cancer and cardiovascular disease, and is closely related to the occurrence and progression of various systemic diseases. However, elucidating the processes of periodontal disease and promoting periodontal bone regeneration remains a challenge. Here, quercetin is demonstrated to reduce the oxidative stress state of orofacial mesenchymal stem cells (OMSCs) in vitro and to affect the osteogenic growth of OMSCs through molecular mechanisms that mediate the m6A change in Per1. Nevertheless, the limited therapeutic efficacy of systemic medication and the limitations of local medication resulting from the small, moist, and highly dynamic periodontal environment make it challenging to treat periodontal tissues with medication. Herein, a biosafe injectable hydrogel drug-controlled delivery system is constructed as a bone-enhancing factory and loaded with quercetin to treat oxidative stress injury in periodontal tissues. This drug-carrying system made up of nanoscale bioglass microspheres and a light-cured injectable hydrogel, allows effective drug particle loading and cementation in the dynamic and moist periodontal environment. Furthermore, the system demonstrates the ability to stimulate OMSCs osteogenic differentiation in a Per1-dependent manner, which ultimately promotes periodontal bone repair, suggesting that this system has potential for clinical periodontal therapy.
Keyphrases
- oxidative stress
- mesenchymal stem cells
- drug delivery
- bone regeneration
- hyaluronic acid
- cardiovascular disease
- tissue engineering
- bone mineral density
- wound healing
- bone marrow
- dna damage
- healthcare
- gene expression
- soft tissue
- stem cells
- signaling pathway
- body composition
- postmenopausal women
- bone loss
- coronary artery disease
- cell therapy
- squamous cell carcinoma
- papillary thyroid
- high resolution
- climate change
- atomic force microscopy
- childhood cancer
- endoplasmic reticulum stress
- replacement therapy
- tandem mass spectrometry
- molecularly imprinted