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Mitochondrial matrix delivery using MITO-Porter, a liposome-based carrier that specifies fusion with mitochondrial membranes

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/45098

Title: Mitochondrial matrix delivery using MITO-Porter, a liposome-based carrier that specifies fusion with mitochondrial membranes
Authors: Yasuzaki, Yukari Browse this author
Yamada, Yuma Browse this author →KAKEN DB
Harashima, Hideyoshi Browse this author
Keywords: Mitochondria
Mitochondrial matrix delivery
Mitochondrial drug delivery
Mitochondrial gene therapy
MITO-Porter
Membrane fusion
mtDNA
Issue Date: 25-Jun-2010
Publisher: Elsevier
Journal Title: Biochemical and Biophysical Research Communications
Volume: 397
Issue: 2
Start Page: 181
End Page: 186
Publisher DOI: 10.1016/j.bbrc.2010.05.070
PMID: 20580633
Abstract: Mitochondria are the principal producers of energy in cells of higher organisms. It was recently reported that mutations and defects in mitochondrial DNA (mtDNA) are associated with various mitochondrial diseases including a variety of neurodegenerative and neuromuscular diseases. Therefore, an effective mitochondrial gene therapy and diagnosis would be expected to have great medical benefits. To achieve this, therapeutic agents need to be delivered into the innermost mitochondrial space (mitochondrial matrix), which contains the mtDNA pool. We previously reported on the development of MITO-Porter, a liposome-based carrier that introduces macromolecular cargos into mitochondria via membrane fusion. In this study, we provide a demonstration of mitochondrial matrix delivery and the visualization of mitochondrial genes (mtDNA) in living cells using the MITO-Porter. We first prepared MITO-Porter containing encapsulated propidium iodide (PI), a fluorescent dye used to stain nucleic acids to detect mtDNA. We then confirmed the emission of red-fluorescence from PI by conjugation with mtDNA, when the carriers were incubated in the presence of isolated rat liver mitochondria. Finally, intracellular observation by confocal laser scanning microscopy clearly verified that the MITO-Porter delivered PI to the mitochondrial matrix.
Type: article (author version)
URI: http://hdl.handle.net/2115/45098
Appears in Collections:薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 山田 勇磨

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