用于引导骨质疏松性骨再生的氧化石墨烯装饰微孔磺化聚醚醚酮。

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
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引用次数: 0

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含吡啶结构域的 3(NLRP3)炎性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)纳米片进行的 RNA 测序发现,GO 纳米材料与 NLRP3 炎性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改性(SPEEK@PDA-GO),在微孔磺化聚醚醚酮(SPEEK)表面构建骨微环境响应性多功能二维GO涂层。体外分析表明,SPEEK@PDA-GO植入物削弱了巨噬细胞中由STAT3介导的NLRP3/caspase-1/IL-1β信号通路,从而阻止了对破骨细胞生成至关重要的细胞外炎性微环境的形成。SPEEK@PDA-GO的M2巨噬细胞标志物和成骨基因表达量明显提高,表明多功能GO纳米片可通过其免疫调节特性促进骨再生。研究还分析了SPEEK@PDA-GO刺激新骨形成和阻断因卵巢切除术导致雌激素丧失引起的骨丢失的能力。这项研究的结果为NLRP3炎性体可能参与骨质疏松症患者免疫系统与骨骼健康之间的相互作用提供了宝贵的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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