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短尾相关蛋白激活的岩藻依聚糖水凝胶微球可恢复退变椎间盘微环境。

Brachyury-Activated Fucoidan Hydrogel Microspheres Rejuvenate Degenerative Intervertebral Discs Microenvironment.

作者信息

Gong Yuhao, Shi Wenxiao, Liu Xingzhu, Yu Hang, Wu Yinghui, Xia Yanzhang, Yue Caichun, Yang Chongkai, Shen Cong, Pei Renjun, Xin Tianwen, Pei Hailong, Shen Jun

机构信息

Department of Orthopedics, the Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou, 215006, P. R. China.

Suzhou Key Laboratory of Orthopedic Medical Engineering, the Affiliated Suzhou Hospital of Nanjing Medical University,Suzhou Municipal Hospital, Suzhou, 215006, P. R. China.

出版信息

Adv Sci (Weinh). 2025 Sep;12(34):e04195. doi: 10.1002/advs.202504195. Epub 2025 Jun 20.

Abstract

Extracellular matrix (ECM) metabolic disorders and the establishment of inflammatory microenvironment are the primary pathological alterations associated with intervertebral disc degeneration (IVDD). The inflammatory microenvironment promotes ECM degradation, further exacerbating the vicious cycle of nucleus pulposus (NP) degeneration. This study introduces the mRNA encoding a novel therapeutic transcription factor, Brachyury (Bry), into nucleus pulposus cells (NPCs) using an injectable microsphere system composed of biomimetic GelMA/Fucoidan (FU) dual-component hydrogel (GF) and surface chemically grafted lipid nanoparticles (LNP) (BLNP@GF). The study aims to alleviate inflammatory response in the NP while restoring the ECM secretion function of NPCs and enhancing the ability of NPCs to withstand inflammatory stress, thereby restoring physiological balance in the NP microenvironment. The GF microspheres demonstrate injectability and porosity, facilitating efficient LNP loading through chemical grafting. In the LPS-simulated inflammatory microenvironment, sustained release of FU significantly reduces inflammatory activity in NPCs. Successful transfection with Bry mRNA upregulate ECM synthesis in degenerated NPCs. In a rat tail puncture IVDD model, local application of BLNP@GF microspheres effectively improved ECM remodeling in NP tissue, thereby ameliorating puncture-induced IVDD. In conclusion, FU-functionalized GelMA hydrogel microspheres loaded with Bry mRNA provide a promising new strategy for reversing IVDD.

摘要

细胞外基质(ECM)代谢紊乱和炎症微环境的建立是与椎间盘退变(IVDD)相关的主要病理改变。炎症微环境促进ECM降解,进一步加剧髓核(NP)退变的恶性循环。本研究使用由仿生甲基丙烯酰化明胶/岩藻依聚糖(FU)双组分水凝胶(GF)和表面化学接枝脂质纳米颗粒(LNP)组成的可注射微球系统(BLNP@GF),将编码新型治疗性转录因子短尾相关转录因子(Bry)的mRNA导入髓核细胞(NPCs)。该研究旨在减轻NP中的炎症反应,同时恢复NPCs的ECM分泌功能,增强NPCs抵抗炎症应激的能力,从而恢复NP微环境中的生理平衡。GF微球具有可注射性和孔隙率,通过化学接枝促进LNP的有效负载。在脂多糖模拟的炎症微环境中,FU的持续释放显著降低了NPCs中的炎症活性。Bry mRNA的成功转染上调了退变NPCs中ECM的合成。在大鼠尾部穿刺IVDD模型中,局部应用BLNP@GF微球有效改善了NP组织中的ECM重塑,从而改善了穿刺诱导的IVDD。总之,负载Bry mRNA的FU功能化甲基丙烯酰化明胶水凝胶微球为逆转IVDD提供了一种有前景的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ea2/12442695/c44caa8c8388/ADVS-12-e04195-g010.jpg

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