Nanozyme Coating-Mediated Mitochondrial Metabolic Reprogramming of Macrophages for Immunomodulatory Osseointegration in Rheumatoid Arthritis Case.

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-07-08 DOI:10.1021/acsnano.5c07535
Shimeng Chen,Xiaoqi Liu,Wenhui Zhang,Bo Li,Fuwei Liu,Yingang Zhang,Yong Han
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引用次数: 0

Abstract

Conventional titanium (Ti)-based implants often fail to achieve osseointegration in bone defects accompanied by rheumatoid arthritis (RA), primarily due to the RA pathological microenvironment, characterized by elevated reactive oxygen species (ROS) levels and hypoxia. This microenvironment induces mitochondria dysfunction and intracellular Ca2+ overload, facilitating macrophage polarization toward the M1 phenotype and thus impairing osteoimmunomodulatory osseointegration. To address this challenge, a nanozyme-inspired coating, featuring the deposition of MnFe2O4 nanoparticles onto a polydopamine (PDA)-decorated surface of microporous TiO2, is constructed on Ti (known as MFO coating). The osteoimmunomodulatory osseointegration of the coating, both in vitro and in vivo, accompanied by RA was assessed, and the underlying mechanisms were also investigated. Due to the efficient conversion of H2O2 into O2 and robust ROS-scavenging capabilities, the coating mitigates mitochondria ROS accumulation and intracellular Ca2+ overload induced by the pathological microenvironment, while simultaneously elevating intracellular O2 levels, thereby preventing macrophage apoptosis. Meanwhile, by improving the microenvironment, the coating activates moderate mitophagy through the Ca2+-AMPK-mTOR signaling pathway, facilitating the removal of dysfunctional mitochondria and the preservation of mitochondrial dynamics and integrity. As a result, the restored mitochondria reprogram their metabolic pathway from relying on anaerobic to relying on aerobic oxidative phosphorylation, facilitating macrophage polarization toward the M2 phenotype, which not only inhibits osteoclastogenesis but also accelerates osseointegration in rats with RA. The coating presents a transformative approach to Ti-based implant design for bone defects associated with inflammatory diseases, potentially reducing the risk of revision surgery and offering a long-lasting lifespan for patients.
纳米酶包被介导的巨噬细胞线粒体代谢重编程对类风湿关节炎患者免疫调节性骨整合的影响。
在类风湿性关节炎(RA)伴有骨缺损的情况下,传统的钛(Ti)基植入物往往无法实现骨整合,这主要是由于RA的病理微环境(以活性氧(ROS)水平升高和缺氧为特征)。这种微环境诱导线粒体功能障碍和细胞内Ca2+超载,促进巨噬细胞向M1表型极化,从而损害骨免疫调节的骨整合。为了解决这一挑战,一种纳米酶启发的涂层,其特点是将MnFe2O4纳米颗粒沉积在聚多巴胺(PDA)修饰的微孔TiO2表面上,构建在Ti上(称为MFO涂层)。在体外和体内评估了涂层的骨免疫调节骨整合,并对其潜在机制进行了研究。由于有效地将H2O2转化为O2和强大的ROS清除能力,该涂层减轻了病理性微环境诱导的线粒体ROS积累和细胞内Ca2+超载,同时提高细胞内O2水平,从而防止巨噬细胞凋亡。同时,通过改善微环境,涂层通过Ca2+-AMPK-mTOR信号通路激活适度的线粒体自噬,促进功能障碍线粒体的去除,保持线粒体动力学和完整性。因此,修复后的线粒体将其代谢途径从依赖厌氧转变为依赖有氧氧化磷酸化,促进巨噬细胞向M2表型极化,这不仅抑制了RA大鼠的破骨细胞生成,而且加速了骨整合。该涂层为炎性疾病相关骨缺损的钛基植入设计提供了一种革命性的方法,潜在地降低了翻修手术的风险,并为患者提供了更长的寿命。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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