Circadian Clock Regulation via Biomaterials for Nucleus Pulposus

被引:36
作者
Chen, Wei [1 ,2 ]
Zheng, Dandan [2 ]
Chen, Hao [2 ]
Ye, Tingjun [1 ]
Liu, Zhihong [1 ]
Qi, Jin [1 ]
Shen, Hongxing
Ruan, Huitong [1 ]
Cui, Wenguo [1 ]
Deng, Lianfu [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Traumatol & Orthopaed, Dept Orthopaed,Sch Med,Shanghai Key Lab Prevent &, 197 Ruijin 2nd Rd, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Dept Spine Surg, Sch Med, 160 Pujian Rd, Shanghai 200127, Peoples R China
基金
国家重点研发计划;
关键词
circadian clock; extracellular matrices; intervertebral disc degeneration; microfluidics; tissue regeneration; DISC DEGENERATION; RHYTHMS;
D O I
10.1002/adma.202301037
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Circadian clock disorder during tissue degeneration has been considered the potential pathogenesis for various chronic diseases, such as intervertebral disc degeneration (IVDD). In this study, circadian clock-regulating biomaterials (ClockMPs) that can effectively activate the intrinsic circadian clock of nucleus pulposus cells (NPCs) in IVDD and improve the physiological function of NPCs for disc regeneration are fabricated via air-microfluidic technique and the chemical cross-linking between polyvinyl alcohol and modified-phenylboronic acid. In vitro experiments verified that ClockMPs can scavenge reactive oxygen species to maintain a stable microenvironment for the circadian clock by promoting the binding of BMAL1 and CLOCK proteins. ClockMPs can regulate the expression of core circadian clock genes by activating the PI3K-AKT pathway in NPCs to remodel the intrinsic circadian clock and promote extracellular matrix synthesis. Furthermore, in vivo experiments of IVDD treated with ClockMPs proved that ClockMPs can promote disc regeneration by regulating the circadian clock of NPCs. In conclusion, ClockMPs provided a novel and promising strategy for circadian clock regulation during tissue regeneration.
引用
收藏
页数:14
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