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GM@mTG-V微球通过重建椎间盘生物力学和炎症微环境促进椎间盘再生。

GM@mTG-V microspheres promote NP regeneration by reconstructing IVD biomechanics and inflammatory microenvironment.

作者信息

Gao Rong, Zhang Yongfeng, Deng Bo, Zhang Jiawei, Liang Zhuowen, Wei Zhao, Xu Feng, Ding Tan

机构信息

Department of Orthopedics, Xijing Hospital, The Fourth Military Medical University, Xi'an, Shaanxi 710032, China.

Bioinspired Engineering and Biomechanics Center (BEBC), Xi'an Jiaotong University, Xi'an, 710049, China.

出版信息

Mater Today Bio. 2025 May 23;32:101897. doi: 10.1016/j.mtbio.2025.101897. eCollection 2025 Jun.

DOI:10.1016/j.mtbio.2025.101897
PMID:40502369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12152893/
Abstract

Intervertebral disc degeneration (IVDD) has emerged as a significant global public health challenge, imposing substantial burdens on both individuals and society. Growing evidence suggests that modulating the mechanical microenvironment and alleviating inflammation in degenerated IVDs can promote tissue regeneration. In this study, we integrated natural pharmaceuticals with tissue engineering strategies to develop functionalized microspheres (GM@mTG-V) through microfluidic synthesis, where vanillin - a natural compound with anti-inflammatory and antioxidant properties - was polymerized with gelatin methacryloyl (GelMA, composed of gelatin derived from methyl acrylamide and methacrylate groups). In vitro, the functionalized microspheres not only enhanced vanillin release efficiency but also effectively suppressed inflammatory responses and oxidative stress in nucleus pulposus (NP) cells. By dynamically regulating matrix stiffness, these microspheres could remodel the mechanical microenvironment of degenerated IVD, significantly promoting extracellular matrix (ECM) secretion. In vivo, both 4 week and 8 week IVDD models demonstrated that GM@mTG-V markedly reduced tissue inflammation, accelerated ECM accumulation, and restored IVD structure, as confirmed by radiographic and histological analyses. This study verifies that GM@mTG-V promotes regeneration of degenerated IVD through dual mechanisms: stabilizing mechanical matrix stiffness and suppressing inflammatory microenvironments, providing a novel and promising therapeutic strategy for early stage IVDD.

摘要

椎间盘退变(IVDD)已成为一项重大的全球公共卫生挑战,给个人和社会都带来了沉重负担。越来越多的证据表明,调节退变椎间盘的力学微环境并减轻炎症可促进组织再生。在本研究中,我们将天然药物与组织工程策略相结合,通过微流控合成技术制备了功能化微球(GM@mTG-V),其中香草醛(一种具有抗炎和抗氧化特性的天然化合物)与甲基丙烯酰化明胶(GelMA,由甲基丙烯酰胺和甲基丙烯酸酯基团衍生的明胶组成)聚合。在体外,功能化微球不仅提高了香草醛的释放效率,还能有效抑制髓核(NP)细胞中的炎症反应和氧化应激。通过动态调节基质硬度,这些微球可以重塑退变椎间盘的力学微环境,显著促进细胞外基质(ECM)分泌。在体内,4周和8周的IVDD模型均表明,GM@mTG-V显著减轻了组织炎症,加速了ECM积累,并恢复了椎间盘结构,影像学和组织学分析证实了这一点。本研究证实,GM@mTG-V通过稳定力学基质硬度和抑制炎症微环境这两种机制促进退变椎间盘再生,为早期IVDD提供了一种新颖且有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/beef6e5e175f/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/9cc322185eb9/ga1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/337863d02abf/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/f4526b57128c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/0cb6644fc728/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/f60daf518538/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/35fb18c4c043/gr5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/4a78adbb0898/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/0c7ea994639b/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/beef6e5e175f/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/9cc322185eb9/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/ad9409593228/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/337863d02abf/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/f4526b57128c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/0cb6644fc728/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/f60daf518538/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/35fb18c4c043/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/daad4d2315a5/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/4a78adbb0898/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/0c7ea994639b/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/12152893/beef6e5e175f/gr9.jpg

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KMT2A regulates the autophagy-GATA4 axis through METTL3-mediated mA modification of ATG4a to promote NPCs senescence and IVDD progression.KMT2A 通过 METTL3 介导的 ATG4a 的 mA 修饰调控自噬-GATA4 轴,促进 NPC 衰老和 IVDD 进展。
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