Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Fusion Oriented Research for Disruptive Science and Technology (FOREST) Program, Japan Science and Technology Agency (JST), Japan.
Expert Opin Biol Ther. 2022 Sep;22(9):1209-1219. doi: 10.1080/14712598.2022.2070427. Epub 2022 May 11.
After the emergence of lipid nanoparticles (LNP) containing therapeutic mRNA as vaccines for use against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the clinical usefulness of nucleic acid-encapsulated LNPs is now a fact. In addition to the nucleus and cytoplasm, mitochondria, which have their own genome, are a site where nucleic acids function in the cell. Gene therapies targeting mitochondria are expected to pave the way for the next generation of therapies.
Methods for delivering nucleic acids to mitochondria are needed in order to realize such innovative therapies. However, only a few reports on delivery systems targeting mitochondria have appeared. In this review, we summarize the current state of research on RNA-based therapeutics targeted to mitochondria, with emphasis on mitochondrial RNA delivery therapies and on therapies that involve the use of mitochondrial genome editing devices.
We hope that this review article will focus our attention to this area of research, stimulate more interest in this field of research, and lead to the development of mitochondria-targeted nucleic acid medicine. It has the potential to become a major weapon against urgent and unknown diseases, including SARS-CoV-2 infections.
在含有治疗性 mRNA 的脂质纳米颗粒(LNP)作为针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的疫苗出现后,核酸包裹的 LNP 的临床应用已成为现实。除了细胞核和细胞质,线粒体也具有自己的基因组,是细胞内核酸发挥作用的场所。针对线粒体的基因疗法有望为下一代疗法铺平道路。
为了实现这些创新疗法,需要将核酸递送到线粒体的方法。然而,只有少数关于靶向线粒体的递药系统的报道。在这篇综述中,我们总结了靶向线粒体的基于 RNA 的治疗方法的最新研究进展,重点介绍了线粒体 RNA 递药疗法和涉及使用线粒体基因组编辑装置的疗法。
我们希望这篇综述文章能引起人们对这一研究领域的关注,激发人们对这一研究领域的兴趣,并推动线粒体靶向核酸药物的发展。它有可能成为对抗包括 SARS-CoV-2 感染在内的紧急和未知疾病的主要武器。