生物仿真支架与协同的BMSC向和ROS清理用于线粒体保护和有效的骨缺陷修复
Sheng Yao1, Lian Zeng2, Huan Wang3
1Department of Rehabilitation Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Journal of nanobiotechnology
|February 3, 2026
概括
工程外体向线粒体保护细胞并增强骨修复. 这种新的策略使用复合脚手架改善了大缺陷的骨再生.
科学领域:
- 生物材料科学 生物材料科学
- 再生医学是一种再生医学.
- 细胞生物学 细胞生物学
背景情况:
- 由于植入物效率差,大骨缺陷重建具有挑战性.
- 介质干细胞衍生的外生体显示出骨修复的潜力.
- 目前的策略缺乏有针对性的线粒体保护和细胞招募.
研究的目的:
- 开发一种针对线粒体的外体细胞战略,用于骨缺陷的修复.
- 通过表面功能化和支架集成来增强外体的有效性.
主要方法:
- 骨髓介质干细胞衍生的外体细胞 (BMSCs) 用MitoQ进行了工程设计,用于ROS清理.
- 外体被Apt19S表面装饰,以加强BMSC向.
- 功能化外体 (EM-Apt) 被集成到一个3D打印的β-三酸支架与SIS水凝 (TCP/SIS@EM-Apt).
主要成果:
- 工程外体展示了有针对性的ROS清理和BMSC招募.
- 在大鼠骨缺陷模型中,TCP/SIS@EM-Apt复合物显著增加了骨体积/总体积 (BV/TV) 的1.9倍.
- 脚手架表现出抗炎,血管新生和骨质新生作用.
结论:
- 在复合支架中集成的线粒体向外体,为大骨缺陷重建提供了一个有希望的解决方案.
- 这种协同方法通过多种治疗机制增强了骨再生.
- 该战略为复杂的再生挑战提供了一个新的治疗途径.
更多相关视频
07:48Three-Dimensional In Vitro Biomimetic Model of Neuroblastoma Using Collagen-Based Scaffolds
Published on: July 9, 2021
4.0K
07:53Peptides from Phage Display Library Modulate Gene Expression in Mesenchymal Cells and Potentiate Osteogenesis in Unicortical Bone Defects
Published on: December 10, 2010
18.5K
相关概念视频
Fractures: Bone Repair
5.4K
Treatment for a fracture is based on the type of break, the bone affected, and the patient's age.
Minor fractures with no bone displacement are treated by immobilizing the fractured bone using a cast or splint. However, in the case of fractures with displaced bones, the broken bones are repositioned before immobilization to ensure successful healing without deformation and loss of function. The realignment of fractured bone ends is performed through a process called reduction. If the...
Minor fractures with no bone displacement are treated by immobilizing the fractured bone using a cast or splint. However, in the case of fractures with displaced bones, the broken bones are repositioned before immobilization to ensure successful healing without deformation and loss of function. The realignment of fractured bone ends is performed through a process called reduction. If the...
5.4K
Animal Mitochondrial Genetics
9.3K
Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
9.3K
Export of Mitochondrial and Chloroplast Genes
4.2K
A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred...
4.2K
Mismatch Repair
43.7K
Overview
43.7K
Overview of DNA Repair
33.7K
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...
33.7K
Base Excision Repair
26.4K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
The first step of...
26.4K
