Neurodegeneration and Mitochondria Organelle Transplantation: “A Technology That Proof of Principle Suggest Is Ready for Prime Time”

R. Elliott, X. Jiang
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Abstract

It is known that mitochondrial dysfunction is associated with neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). Researchers have tested the therapeutic efficacy of many mitochondrial targeted agents; however, results have been disappointing without significant impact on disease survival. Several groups have demonstrated that mitochondrial transfer of isolated normal healthy mitochondria to defective calls can restore functional recovery. Our experience with mitochondria organelle transplantation (MOT) in cancer cells led to investigating the technology for neurodegenerative diseases (NDs), especially ALS. The rationale was that if the uptake of normal mitochondria into cancer cells inhibited proliferation and glycolysis; then MOT might be a cell-based therapy for NDs. In this communication, we will present background research on MOT in vitro and in vivo cell culture and animal models respectively. This research evidence showed proof of principle of the technology. This fact led us to try the procedure on a desperate human ALS patient.
神经变性和线粒体细胞器移植:“一项原理证明即将进入黄金时代的技术”
众所周知,线粒体功能障碍与包括肌萎缩性侧索硬化症(ALS)在内的神经退行性疾病有关。研究人员已经测试了许多线粒体靶向药物的治疗效果;然而,结果令人失望,对疾病生存没有显著影响。几个小组已经证明,将分离的正常健康线粒体转移到有缺陷的细胞中可以恢复功能恢复。我们在癌细胞线粒体细胞器移植(MOT)方面的经验促使我们研究神经退行性疾病(NDs),特别是ALS的技术。其基本原理是,如果癌细胞摄取正常线粒体会抑制增殖和糖酵解;那么MOT可能是一种以细胞为基础的nd治疗方法。在这篇通讯中,我们将分别介绍MOT的体外、体内细胞培养和动物模型的背景研究。这一研究证明了该技术的原理。这一事实促使我们在一名绝望的ALS患者身上进行试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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