Rejuvenating Aged Bone Repair Through Multihierarchy Reaction Oxygen Species-Regulated Hydrogel.
Zirui HeChuanhao SunYifan MaXi ChenYing WangKai ChenFangru XieYan ZhangYuan YuanChangsheng LiuPublished in: Advanced materials (Deerfield Beach, Fla.) (2023)
Aging exacerbates the dysfunction of tissue regeneration at multiple levels and gradually diminishes individual's capacity to withstand stress, damage, and disease. The excessive accumulation of reactive oxygen species (ROS) is considered a hallmark feature of senescent stem cells, which causes oxidative stress, deteriorates the host microenvironment, and eventually becomes a critical obstacle for aged bone defect repair. Till now, the strategies cannot synchronously and thoroughly regulate intracellular and extracellular ROS in senescent cells. Herein, we developed a multihierarchy ROS scavenging system for aged bone regeneration by fabricating an injectable PEGylated poly(glycerol sebacate) (PEGS-NH 2 )/poly(γ-glutamic acid) (γ-PGA) hydrogel hydrogel containing rapamycin-loaded poly(diselenide-carbonate) nanomicelles (PSeR). This PSeR hydrogel exhibited highly sensitive ROS responsiveness to the local aged microenvironment and dynamically released drug-loaded nanomicelles to scavenge the intracellular ROS accumulated in senescent bone mesenchymal stem cells. The PSeR hydrogel effectively tuned the antioxidant function and delayed senescence of bone mesenchymal stem cells by safeguarding DNA replication in an oxidative environment, thereby promoting the self-renewal ability and enhancing the osteogenic capacity for aged bone repair in vitro and in vivo. Thus, this multihierarchy ROS-regulated hydrogel provides a new strategy for treating degenerative diseases. This article is protected by copyright. All rights reserved.
Keyphrases
- reactive oxygen species
- drug delivery
- bone regeneration
- stem cells
- mesenchymal stem cells
- wound healing
- dna damage
- oxidative stress
- hyaluronic acid
- bone mineral density
- cell death
- tissue engineering
- soft tissue
- induced apoptosis
- bone loss
- bone marrow
- cancer therapy
- postmenopausal women
- umbilical cord
- emergency department
- cell therapy
- cell cycle arrest
- ischemia reperfusion injury
- body composition
- living cells
- physical activity
- metal organic framework
- drug induced