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通过 MITO-Porter 靶向线粒体基因组:mtDNA 和 mtRNA 水平及线粒体功能的评估。

Targeting the Mitochondrial Genome Via a MITO-Porter : Evaluation of mtDNA and mtRNA Levels and Mitochondrial Function.

机构信息

Laboratory for Molecular Design of Pharmaceutics, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.

出版信息

Methods Mol Biol. 2021;2275:227-245. doi: 10.1007/978-1-0716-1262-0_14.

Abstract

Genetic mutations and defects in mitochondrial DNA (mtDNA) are associated with certain types of mitochondrial dysfunctions, ultimately resulting in the emergence of a variety of human diseases. To achieve an effective mitochondrial gene therapy, it will be necessary to deliver therapeutic agents to the innermost mitochondrial space (the mitochondrial matrix), which contains the mtDNA pool. We recently developed a MITO-Porter, a liposome-based nanocarrier that delivers cargo to mitochondria via a membrane-fusion mechanism. In this chapter, we discuss the methodology used to deliver bioactive molecules to the mitochondrial matrix using a Dual Function (DF)-MITO-Porter, a liposome-based nanocarrier that delivers it cargo by means of a stepwise process, and an evaluation of mtDNA levels and mitochondrial activities in living cells. We also discuss mitochondrial gene silencing by the mitochondrial delivery of antisense RNA oligonucleotide (ASO) targeting mtDNA-encoded mRNA using the MITO-Porter system.

摘要

遗传突变和线粒体 DNA(mtDNA)缺陷与某些类型的线粒体功能障碍有关,最终导致多种人类疾病的出现。为了实现有效的线粒体基因治疗,有必要将治疗剂递送到最内部的线粒体空间(线粒体基质),其中包含 mtDNA 池。我们最近开发了一种 MITO-Porter,这是一种基于脂质体的纳米载体,通过膜融合机制将货物递送到线粒体。在本章中,我们讨论了使用双功能(DF)-MITO-Porter 将生物活性分子递送到线粒体基质的方法,DF-MITO-Porter 是一种基于脂质体的纳米载体,通过逐步过程递送其货物,以及评估活细胞中的 mtDNA 水平和线粒体活性。我们还讨论了使用 MITO-Porter 系统通过线粒体递送来靶向 mtDNA 编码 mRNA 的反义 RNA 寡核苷酸(ASO)进行线粒体基因沉默。

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