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Recent Advances in Mitochondria-Targeted Gene Delivery

Mitochondria are the energy-producing organelles of cells. Mitochondrial dysfunctions link to various syndromes and diseases including myoclonic epilepsy and ragged-red fiber disease (MERRF), Leigh syndrome (LS), and Leber hereditary optic neuropathy (LHON). Primary mitochondrial diseases often resu...

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Detalles Bibliográficos
Autores principales: Jang, Yoon-ha, Lim, Kwang-il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225103/
https://www.ncbi.nlm.nih.gov/pubmed/30208599
http://dx.doi.org/10.3390/molecules23092316
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author Jang, Yoon-ha
Lim, Kwang-il
author_facet Jang, Yoon-ha
Lim, Kwang-il
author_sort Jang, Yoon-ha
collection PubMed
description Mitochondria are the energy-producing organelles of cells. Mitochondrial dysfunctions link to various syndromes and diseases including myoclonic epilepsy and ragged-red fiber disease (MERRF), Leigh syndrome (LS), and Leber hereditary optic neuropathy (LHON). Primary mitochondrial diseases often result from mutations of mitochondrial genomes and nuclear genes that encode the mitochondrial components. However, complete intracellular correction of the mutated genetic parts relevant to mitochondrial structures and functions is technically challenging. Instead, there have been diverse attempts to provide corrected genetic materials with cells. In this review, we discuss recent novel physical, chemical and biological strategies, and methods to introduce genetic cargos into mitochondria of eukaryotic cells. Effective mitochondria-targeting gene delivery systems can reverse multiple mitochondrial disorders by enabling cells to produce functional mitochondrial components.
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spelling pubmed-62251032018-11-13 Recent Advances in Mitochondria-Targeted Gene Delivery Jang, Yoon-ha Lim, Kwang-il Molecules Review Mitochondria are the energy-producing organelles of cells. Mitochondrial dysfunctions link to various syndromes and diseases including myoclonic epilepsy and ragged-red fiber disease (MERRF), Leigh syndrome (LS), and Leber hereditary optic neuropathy (LHON). Primary mitochondrial diseases often result from mutations of mitochondrial genomes and nuclear genes that encode the mitochondrial components. However, complete intracellular correction of the mutated genetic parts relevant to mitochondrial structures and functions is technically challenging. Instead, there have been diverse attempts to provide corrected genetic materials with cells. In this review, we discuss recent novel physical, chemical and biological strategies, and methods to introduce genetic cargos into mitochondria of eukaryotic cells. Effective mitochondria-targeting gene delivery systems can reverse multiple mitochondrial disorders by enabling cells to produce functional mitochondrial components. MDPI 2018-09-11 /pmc/articles/PMC6225103/ /pubmed/30208599 http://dx.doi.org/10.3390/molecules23092316 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jang, Yoon-ha
Lim, Kwang-il
Recent Advances in Mitochondria-Targeted Gene Delivery
title Recent Advances in Mitochondria-Targeted Gene Delivery
title_full Recent Advances in Mitochondria-Targeted Gene Delivery
title_fullStr Recent Advances in Mitochondria-Targeted Gene Delivery
title_full_unstemmed Recent Advances in Mitochondria-Targeted Gene Delivery
title_short Recent Advances in Mitochondria-Targeted Gene Delivery
title_sort recent advances in mitochondria-targeted gene delivery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225103/
https://www.ncbi.nlm.nih.gov/pubmed/30208599
http://dx.doi.org/10.3390/molecules23092316
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