Wang He, Chang Xiaowei, Ma Qian, Sun Boyang, Li Han, Zhou Jinmin, Hu Yiyao, Yang Xiaoyu, Li Jie, Chen Xin, Song Jinlin
Chongqing Key Laboratory of Oral Diseases and Biomedical Sciences, Chongqing Municipal Key Laboratory of Oral Biomedical Engineering of Higher Education, College of Stomatology of Chongqing Medical University, Chongqing, 401147, China.
Department of Chemical Engineering, Shaanxi Key Laboratory of Energy Chemical Process Intensification, Institute of Polymer Science in Chemical Engineering, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an, 710049, China.
Bioact Mater. 2022 Sep 14;21:324-339. doi: 10.1016/j.bioactmat.2022.08.029. eCollection 2023 Mar.
Diabetes mellitus (DM) aggravates periodontitis, resulting in accelerated periodontal bone resorption. Disordered glucose metabolism in DM causes reactive oxygen species (ROS) overproduction resulting in compromised bone healing, which makes diabetic periodontal bone regeneration a major challenge. Inspired by the natural bone healing cascade, a mesoporous silica nanoparticle (MSN)-incorporated PDLLA (poly(dl-lactide))-PEG-PDLLA (PPP) thermosensitive hydrogel with stepwise cargo release is designed to emulate the mesenchymal stem cell "recruitment-osteogenesis" cascade for diabetic periodontal bone regeneration. During therapy, SDF-1 quickly escapes from the hydrogel due to diffusion for early rat bone marrow stem cell (rBMSC) recruitment. Simultaneously, slow degradation of the hydrogel starts to gradually expose the MSNs for sustained release of metformin, which can scavenge the overproduced ROS under high glucose conditions to reverse the inhibited osteogenesis of rBMSCs by reactivating the AMPK/β-catenin pathway, resulting in regulation of the diabetic microenvironment and facilitation of osteogenesis. experiments indicate that the hydrogel markedly restores the inhibited migration and osteogenic capacities of rBMSCs under high glucose conditions. results suggest that it can effectively recruit rBMSCs to the periodontal defect and significantly promote periodontal bone regeneration under type 2 DM. In conclusion, our work provides a novel therapeutic strategy of a bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration.
糖尿病(DM)会加重牙周炎,导致牙周骨吸收加速。糖尿病患者体内紊乱的糖代谢会导致活性氧(ROS)过量产生,从而损害骨愈合,这使得糖尿病性牙周骨再生成为一项重大挑战。受天然骨愈合级联反应的启发,设计了一种含有介孔二氧化硅纳米颗粒(MSN)的聚(dl-丙交酯)-聚乙二醇-聚(dl-丙交酯)(PPP)热敏水凝胶,其具有逐步释放药物的功能,旨在模拟间充质干细胞的“募集-成骨”级联反应,以促进糖尿病性牙周骨再生。在治疗过程中,由于扩散作用,基质细胞衍生因子-1(SDF-1)会迅速从水凝胶中释放出来,用于早期招募大鼠骨髓干细胞(rBMSC)。同时,水凝胶的缓慢降解开始逐渐暴露MSN,以便持续释放二甲双胍,二甲双胍可以在高糖条件下清除过量产生的ROS,通过重新激活AMPK/β-连环蛋白途径来逆转rBMSC的成骨抑制,从而调节糖尿病微环境并促进成骨。实验表明,该水凝胶在高糖条件下能显著恢复rBMSC受到抑制的迁移和成骨能力。结果表明,它可以有效地将rBMSC募集到牙周缺损部位,并在2型糖尿病条件下显著促进牙周骨再生。总之,我们的工作提供了一种新型治疗策略,即一种模仿天然骨愈合级联反应的生物启发式药物递送系统,用于糖尿病性牙周骨再生。