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负载工程外泌体的丝状结构微针通过调节线粒体自噬恢复和细胞外基质稳态来修复纤维环。

Thread-structural microneedles loaded with engineered exosomes for annulus fibrosus repair by regulating mitophagy recovery and extracellular matrix homeostasis.

作者信息

Hu Shaojun, Zhu Meng, Xing Hongyuan, Xue Yucheng, Li Jun, Wang Zhan, Zhu Zhou, Fang Miaojie, Li Zilong, Xu Jianbin, He Yong, Zhang Ning

机构信息

Department of Orthopedic Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou City, Zhejiang Province, PR China.

Orthopedics Research Institute of Zhejiang University, Hangzhou City, Zhejiang Province, PR China.

出版信息

Bioact Mater. 2024 Mar 13;37:1-13. doi: 10.1016/j.bioactmat.2024.03.006. eCollection 2024 Jul.

DOI:10.1016/j.bioactmat.2024.03.006
PMID:38515611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10951295/
Abstract

Low back pain is among the most grave public health concerns worldwide and the major clinical manifestation of intervertebral disc degeneration (IVDD). The destruction of annulus fibrosus (AF) is the primary cause of IVDD. A sustainable and stable treatment system for IVDD is lacking because of the special organizational structure and low nutrient supply of AF. We here found that IVDD results in the impaired mitochondrial function of AF tissue, and mitochondrial autophagy (mitophagy) plays a protective role in this process. We therefore reported a thread-structural microneedle (T-MN) matching the ring structure of AF. Based on the adsorption effect of laminin, our T-MN could load with bone marrow mesenchymal stem cell-derived exosomes to envelope the regulating mitophagy microRNA (miRNA 378), named as T-MN. In general, we offered in situ locking in the defect site of AF to prevent nucleus pulposus leakage and promoted AF repair. The design of the thread structure was aimed at bionically matching the layered AF structure, thereby providing stronger adhesion. The T-MN effectively attached to AF and slowly released therapeutic engineered exosomes, and prevented IVDD progression by restoring mitophagy, promoting AF cell proliferation and migration, and inhibiting the pathological remodeling of the extracellular matrix. This functional system can be used as an excellent tool for sustained drug release and has a certain prospect in substituting the conventional treatment of IVDD.

摘要

腰痛是全球最严重的公共卫生问题之一,也是椎间盘退变(IVDD)的主要临床表现。纤维环(AF)的破坏是IVDD的主要原因。由于AF特殊的组织结构和低营养供应,目前缺乏一种可持续且稳定的IVDD治疗系统。我们在此发现IVDD会导致AF组织的线粒体功能受损,而线粒体自噬(mitophagy)在此过程中发挥保护作用。因此,我们报道了一种与AF环结构相匹配的线状结构微针(T-MN)。基于层粘连蛋白的吸附作用,我们的T-MN可以负载骨髓间充质干细胞来源的外泌体,包裹调节线粒体自噬的微小RNA(miRNA 378),命名为T-MN。总体而言,我们提供了在AF缺损部位的原位锁定,以防止髓核渗漏并促进AF修复。线状结构的设计旨在仿生匹配分层的AF结构,从而提供更强的附着力。T-MN有效地附着于AF并缓慢释放治疗性工程外泌体,通过恢复线粒体自噬、促进AF细胞增殖和迁移以及抑制细胞外基质的病理重塑来防止IVDD进展。这种功能系统可作为一种优秀的持续药物释放工具,在替代IVDD的传统治疗方面具有一定的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/9493656eeab1/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/55ab8075c902/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/003fd19a289d/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/41e7075ced78/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/7373d737b147/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/56caa81a9da1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/d47772ddcf94/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/517c4983dc1e/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/9493656eeab1/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/55ab8075c902/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/003fd19a289d/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/41e7075ced78/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/7373d737b147/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/56caa81a9da1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/d47772ddcf94/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/517c4983dc1e/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/255a/10951295/9493656eeab1/gr6.jpg

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