Wei Runxiu, Chen Yiman, Yang Qiang, Wang Tongge, He Yanyun, Yin Na, Yang Liya, Gao Yifei, Guo Ling, Feng Min
School of Pharmaceutical Sciences, Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, Sun Yat-Sen University, University Town, Guangzhou 510006, China.
Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, China.
ACS Nano. 2025 Feb 4;19(4):4403-4421. doi: 10.1021/acsnano.4c12557. Epub 2025 Jan 24.
Mitochondrial transplantation is a significant therapeutic approach for addressing mitochondrial dysfunction in patients with spinal cord injury (SCI), yet it is limited by rapid mitochondrial deactivation and low transfer efficiency. Here, high-quality mitochondria microfactories (HQ-Mitofactories) were constructed by anchoring Prussian blue nanoenzymes onto mesenchymal stem cells for effective mitochondrial transplantation to treat paralysis from SCI. Notably, the results demonstrated that HQ-Mitofactories could continuously produce vitality-boosting mitochondria with highly interconnected and elongated network structures under oxidative stress by scavenging excessive ROS. Furthermore, HQ-Mitofactories enabled efficient transfer of therapeutic mitochondria to injured neurons primarily via gap junctions, resulting in the restoration of mitochondrial homeostasis and thereby suppressing intracellular ROS burst and facilitating neuronal repair. After administration, HQ-Mitofactories migrated to the injured spinal cords of SCI mice and subsequently promoted neuronal regeneration and remyelination. Consequently, HQ-Mitofactory-treated mice successfully recovered locomotor function within 4 weeks, with 40% of the mice fully restoring walking after hindlimb paralysis. Conversely, untreated SCI exhibited completely abolished hindlimb movements. In light of real-time generation of vitality-boosting mitochondria even under oxidative stress and enabling targeted mitochondrial transfer, HQ-Mitofactories have promising therapeutic potential in the context of mitochondrial transplantation to reduce SCI-related paralysis, and more broadly impact the field of neuroregenerative medicine.
线粒体移植是治疗脊髓损伤(SCI)患者线粒体功能障碍的一种重要治疗方法,但它受到线粒体快速失活和低转移效率的限制。在此,通过将普鲁士蓝纳米酶锚定在间充质干细胞上构建了高质量线粒体微工厂(HQ-线粒体微工厂),用于有效的线粒体移植以治疗SCI引起的瘫痪。值得注意的是,结果表明HQ-线粒体微工厂能够在氧化应激下通过清除过量的活性氧(ROS),持续产生具有高度互连和细长网络结构的增强活力的线粒体。此外,HQ-线粒体微工厂主要通过缝隙连接将治疗性线粒体高效转移至受损神经元,从而恢复线粒体稳态,进而抑制细胞内ROS爆发并促进神经元修复。给药后,HQ-线粒体微工厂迁移至SCI小鼠的受损脊髓,随后促进神经元再生和髓鞘再生。因此,经HQ-线粒体微工厂治疗的小鼠在4周内成功恢复运动功能,40%的小鼠在后肢瘫痪后完全恢复行走。相反,未经治疗的SCI小鼠后肢运动完全丧失。鉴于即使在氧化应激下也能实时产生增强活力的线粒体并实现靶向线粒体转移,HQ-线粒体微工厂在减少SCI相关瘫痪的线粒体移植背景下具有广阔的治疗潜力,并更广泛地影响神经再生医学领域。