Wang Xuechun, Wang Qing, Wang Jian, Wang Xuan, Yin Linling, Wang Changping, Fan Guangjian, Pan Jinsong
Department of Stomatology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 201620, China.
Department of General Dentistry, Shanghai Ninth People's Hospital, School of Medicine, College of Stomatology, Shanghai Jiao Tong University, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Sciences, Shanghai, 200011, China.
Biomater Res. 2024 Jul 29;28:0057. doi: 10.34133/bmr.0057. eCollection 2024.
Periodontitis is a chronic inflammatory disease characterized by plaque accumulation, resulting in immune microenvironment disorders and resorption of alveolar bone. To promote bone healing under inflammatory environments, a functional biomaterial based on disease pathophysiology is designed. A novel fatty acid C10-modified polypeptide, C-KR8, is discovered to have excellent abilities in modulating macrophage repolarization and promoting bone regeneration in periodontitis. To build a multifunctional material localized drug delivery system, C-KR8@ZIF-8 (C-KR8-loaded zeolitic imidazolate framework-8) nanoparticles are constructed to sustainedly release the C-KR8 peptide and Zn elements. By synergistic effects of providing a dynamic immuno-modulatory environment and promoting osteogenesis under pathological conditions, the obtained pH-responsive nanoparticles display excellent bone regeneration capability. Furthermore, coimmunoprecipitation/liquid chromatography-tandem mass spectrometry analysis and proteomics analysis revealed that the C-KR8 peptide directly interacts with the high-temperature requirement protein A1 (Htra1), and C-KR8@ZIF-8 nanoparticles promote the osteogenic differentiation of bone mesenchymal stem cells by activating the focal adhesion kinase (FAK)/phosphatidylinositide 3-kinase (PI3K)/AKT pathway and enhancing the nuclear localization of Yes-associated protein (YAP). Taken together, this study demonstrates C-KR8 peptide regulate osteoimmunology and bone regeneration by Htra1/FAK/YAP pathway and that ZIF-8-based peptide loading platform is a promising strategy for periodontitis.
牙周炎是一种以菌斑积聚为特征的慢性炎症性疾病,会导致免疫微环境紊乱和牙槽骨吸收。为了促进炎症环境下的骨愈合,基于疾病病理生理学设计了一种功能性生物材料。发现一种新型脂肪酸C10修饰的多肽C-KR8在调节巨噬细胞极化和促进牙周炎骨再生方面具有优异能力。为构建多功能材料局部给药系统,制备了C-KR8@ZIF-8(负载C-KR8的沸石咪唑酯骨架-8)纳米颗粒以持续释放C-KR8肽和锌元素。通过在病理条件下提供动态免疫调节环境和促进成骨的协同作用,所获得的pH响应性纳米颗粒显示出优异的骨再生能力。此外,免疫共沉淀/液相色谱-串联质谱分析和蛋白质组学分析表明,C-KR8肽直接与高温需求蛋白A1(Htra1)相互作用,并且C-KR8@ZIF-8纳米颗粒通过激活粘着斑激酶(FAK)/磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(AKT)途径并增强Yes相关蛋白(YAP)的核定位来促进骨间充质干细胞的成骨分化。综上所述,本研究证明C-KR8肽通过Htra1/FAK/YAP途径调节骨免疫学和骨再生,并且基于ZIF-8的肽负载平台是治疗牙周炎的一种有前景的策略。