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聚芳醚醚酮表面的程序化设计可启动免疫调节并依次实现骨再生。

Programmed surface on poly(aryl-ether-ether-ketone) initiating immune mediation and fulfilling bone regeneration sequentially.

作者信息

Xie Lingxia, Wang Guomin, Wu Yuzheng, Liao Qing, Mo Shi, Ren Xiaoxue, Tong Liping, Zhang Wei, Guan Min, Pan Haobo, Chu Paul K, Wang Huaiyu

机构信息

Center for Human Tissues and Organs Degeneration, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.

Department of Physics, Department of Materials Science and Engineering, and Department of Biomedical Engineering, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China.

出版信息

Innovation (Camb). 2021 Aug 5;2(3):100148. doi: 10.1016/j.xinn.2021.100148. eCollection 2021 Aug 28.

Abstract

The immune responses are involved in every stage after implantation but the reported immune-regulated materials only work at the beginning without fully considering the different phases of bone healing. Here, poly(aryl-ether-ether-ketone) (PEEK) is coated with a programmed surface, which rapidly releases interleukin-10 (IL-10) in the first week and slowly delivers dexamethasone (DEX) up to 4 weeks. Owing to the synergistic effects of IL-10 and DEX, an aptly weak inflammation is triggered within the first week, followed by significant M2 polarization of macrophages and upregulation of the autophagy-related factors. The suitable immunomodulatory activities pave the way for osteogenesis and the steady release of DEX facilitates bone regeneration thereafter. The sequential immune-mediated process is also validated by an 8-week implementation on a rat model. This is the first attempt to construct implants by taking advantage of both immune-mediated modulation and sequential regulation spanning all bone regeneration phases, which provides insights into the fabrication of advanced biomaterials for tissue engineering and immunological therapeutics.

摘要

免疫反应参与植入后的每个阶段,但报道的免疫调节材料仅在开始时起作用,未充分考虑骨愈合的不同阶段。在此,聚芳醚醚酮(PEEK)被赋予了一个程序化表面,该表面在第一周快速释放白细胞介素-10(IL-10),并在长达4周的时间内缓慢递送地塞米松(DEX)。由于IL-10和DEX的协同作用,在第一周内引发了适度的弱炎症,随后巨噬细胞发生显著的M2极化以及自噬相关因子上调。合适的免疫调节活性为骨生成铺平了道路,DEX的持续释放促进了随后的骨再生。这种顺序性免疫介导过程也通过在大鼠模型上进行的8周实验得到了验证。这是首次尝试利用免疫介导调节和跨越所有骨再生阶段的顺序调节来构建植入物,为组织工程和免疫治疗的先进生物材料制造提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b22/8454576/0a050cc44d1d/fx1.jpg

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