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基于 mA 依赖方式通过 METTL3/Clip3 抑制衰老来减少辐射诱导的骨损伤的碳点。

Carbon Dots from Attenuate Radiation-Induced Bone Injury by Inhibiting Senescence via METTL3/Clip3 in an mA-Dependent Manner.

机构信息

Department of Oromaxillofacial-Head & Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, College of Stomatology, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, Shanghai Jiao Tong University, Shanghai 200011, China.

出版信息

ACS Appl Mater Interfaces. 2023 May 3;15(17):20726-20741. doi: 10.1021/acsami.3c01322. Epub 2023 Apr 23.

Abstract

Radiation-induced bone injury management remains a challenge in clinical practice, and there is no effective medicine. Recently, biomass-derived carbon dots (CDs) have attracted attention in biomedical engineering due to the advantages of abundant heteroatoms, low toxicity, and no need to drug loading. Here, we report that CDs, synthesized from via hydrothermal strategy, can effectively alleviate radiation-induced bone injury. CCK-8, apoptosis analysis, β-galactosidase staining, quantitative polymerase chain reaction, and western blots demonstrate that CDs can mediate radiation-induced damage and senescence of bone marrow mesenchymal stem cells (BMSCs). CDs regulate osteogenic- and adipogenic-balance after irradiation, shown by alizarin red and oil red O staining. In vivo experiments reveal that CDs prevent the occurrence of osteoradionecrosis in rats, demonstrated by micro-CT and histology examination. The osseointegration of titanium implants installed in irradiated bone is promoted by CDs. Mechanistically, CDs increase the 6-methyladenosine (mA) level of irradiated BMSCs via the increased methyltransferase-like 3 (METTL3). High-throughput sequencing facilitates detection of increased mA levels located in the 3'-untranslated regions (UTR) of the CAP-Gly domain containing linker protein 3 (Clip3) mRNA. The dual-luciferase reporter assay shows that 3'UTR is the direct target of METTL3. Subsequently, the increased mA modification led to enhanced degradation of mRNA and downregulated CLIP3 expression, eventually resulting in the alleviation of radiation-induced bone injury. Interfering with the METTL3/Clip3 axis can antagonize the effect of CDs, indicating that CDs mediate radiation-induced bone injury via the METTL3/Clip3 axis. Taken together, CDs from alleviate radiation-induced bone injury by inhibiting senescence via regulation of mA modification of . The present study paves a new pathway for the management of radiation-induced bone injury.

摘要

辐射诱导性骨损伤的管理在临床实践中仍然是一个挑战,目前尚无有效的治疗药物。最近,生物量衍生的碳点(CDs)由于其富含杂原子、低毒性和无需药物加载的优点,在生物医学工程中引起了关注。在这里,我们报告说,通过水热策略从 合成的 CDs 可以有效地缓解辐射诱导的骨损伤。CCK-8、细胞凋亡分析、β-半乳糖苷酶染色、定量聚合酶链反应和 Western blot 表明,CDs 可以介导骨髓间充质干细胞(BMSCs)的辐射损伤和衰老。CDs 调节照射后成骨和成脂平衡,通过茜素红和油红 O 染色显示。体内实验表明,CDs 通过微 CT 和组织学检查预防大鼠骨放射性坏死的发生。CDs 促进植入照射骨中的钛植入物的骨整合。机制上,CDs 通过增加甲基转移酶样 3(METTL3)增加照射 BMSCs 中的 6-甲基腺苷(mA)水平。高通量测序有助于检测到 Clip3 mRNA 的 3'UTR 中 mA 水平的增加。双荧光素酶报告基因检测显示 3'UTR 是 METTL3 的直接靶标。随后,增加的 mA 修饰导致 mRNA 的降解增强,CLIP3 表达下调,最终缓解了辐射诱导的骨损伤。干扰 METTL3/Clip3 轴可以拮抗 CD 的作用,表明 CD 通过 METTL3/Clip3 轴介导辐射诱导的骨损伤。总之,来自 的 CDs 通过调节 mA 修饰来抑制衰老,从而缓解辐射诱导的骨损伤。本研究为辐射诱导性骨损伤的管理开辟了一条新途径。

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