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氧化石墨烯修饰的微孔磺化聚醚醚酮用于指导骨质疏松性骨再生。

Graphene oxide-decorated microporous sulfonated polyetheretherketone for guiding osteoporotic bone regeneration.

机构信息

Department of Orthopedics, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200233, China.

Department of Orthopedics, Nanjing Jinling Hospital, Affliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu Province, China.

出版信息

J Control Release. 2024 Oct;374:15-27. doi: 10.1016/j.jconrel.2024.07.054. Epub 2024 Aug 7.

Abstract

Recent studies have indicated that the nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome is an ideal therapeutic target for osteoporosis because it affects the differentiation of osteoblasts and osteoclasts. RNA sequencing utilizing multifunctional graphene oxide (GO) nanosheets revealed a correlation between GO nanomaterials and the NLRP3 inflammasome, as well as osteogenic genes in macrophages. This study aimed to construct a bone microenvironment-responsive multifunctional two-dimensional GO coating on the surface of microporous sulfonated polyetheretherketone (SPEEK) via polydopamine modification (SPEEK@PDA-GO). In vitro analysis showed that the SPEEK@PDA-GO implants weakened the STAT3-mediated NLRP3/caspase-1/IL-1β signaling pathway in macrophages and subsequently prevented the formation of an extracellular inflammatory microenvironment, which is crucial for osteoclastogenesis. SPEEK@PDA-GO displayed significantly higher expression of M2 macrophage markers and osteogenic genes, indicating that the multifunctional GO nanosheets could facilitate bone regeneration via their immunomodulatory properties. The ability of SPEEK@PDA-GO to stimulate new bone formation and block bone loss caused by estrogen loss due to ovariectomy was also analyzed. The findings of this study offer valuable information on the possible involvement of the NLRP3 inflammasome in the interaction between the immune system and bone health in patients with osteoporosis.

摘要

最近的研究表明,核苷酸结合寡聚化结构域样受体家族富含吡咯结构域蛋白 3(NLRP3)炎症小体是骨质疏松症的理想治疗靶点,因为它影响成骨细胞和破骨细胞的分化。利用多功能氧化石墨烯(GO)纳米片进行 RNA 测序表明,GO 纳米材料与 NLRP3 炎症小体以及巨噬细胞中的成骨基因之间存在相关性。本研究旨在通过聚多巴胺修饰(SPEEK@PDA-GO)在微孔磺化聚醚醚酮(SPEEK)表面构建一种对骨微环境响应的多功能二维 GO 涂层。体外分析表明,SPEEK@PDA-GO 植入物减弱了 STAT3 介导的巨噬细胞中 NLRP3/caspase-1/IL-1β信号通路,从而防止了破骨细胞形成细胞外炎症微环境,这对于破骨细胞形成至关重要。SPEEK@PDA-GO 显示出更高水平的 M2 巨噬细胞标志物和成骨基因的表达,表明多功能 GO 纳米片可以通过其免疫调节特性促进骨再生。还分析了 SPEEK@PDA-GO 刺激新骨形成和阻断去卵巢引起的雌激素缺乏导致的骨丢失的能力。本研究的结果提供了有关 NLRP3 炎症小体可能参与骨质疏松症患者免疫系统和骨骼健康之间相互作用的有价值信息。

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