idw – Informationsdienst Wissenschaft

Nachrichten, Termine, Experten

Grafik: idw-Logo
Science Video Project
idw-Abo

idw-News App:

AppStore

Google Play Store



Instance:
Share on: 
09/25/2018 11:22

Proof of Concept: Gene therapy for mitochondrial diseases

Dr. Annegret Burkert Communications
Max-Planck-Institut für Biologie des Alterns

    Mitochondrial disease is now thought to be the second most commonly diagnosed genetic disease worldwide, and, unfortunately, there are still no proven treatment strategies for those diagnosed. Scientists from the Max Planck Institute for Biology of Ageing in Cologne were involved in collaborations to apply gene-therapy approaches in mice to successfully treat an animal model of mitochondrial disease. This may pave the way for future therapeutic strategies for patients.

    Every step we take, every laugh we make, every word we say requires energy. Mitochondria play a central role in our metabolism and energy production. Consequently, mitochondrial dysfunction causes a remarkably diverse group of metabolic diseases with a broad range of symptoms leading to severe disability. “Since the 1980s it was known that mutations in the mitochondrial DNA can lead to disease” explains James Stewart, group leader at the Max Planck Institute for Biology of Ageing and continues “we have known of these patients for over 30 years and only now are we starting to develop treatments”.

    A remarkable feature of mitochondria is that they contain their own DNA. Mutations in this mitochondrial DNA (mtDNA) can lead to mitochondrial diseases, but whether a person with a mutation develops disease or not is more complex. Many copies of mtDNA are present in each of our cells and, normally, disease-causing mutations are present in only a fraction of them. However, if the fraction of mutated mtDNA molecules rises above a certain threshold, mitochondrial function is compromised resulting in mitochondrial disease. Therefore, reducing the levels of mutated mtDNA molecules is a potential treatment strategy.

    However, this treatment strategy is not so straightforward as conventional gene-therapy approaches do not work in mtDNA. Scientists from the University of Cambridge, UK and the University of Miami, USA, developed an approach to specifically degrade mutated mtDNA molecules in cell culture. Using a modified virus, they delivered a gene into the cell nucleus that encodes a protein that works as molecular scissors. These molecular scissors are then produced by the cell and targeted to mitochondria, where they specifically cut the mutated mtDNA.

    But would the method also work in complex organisms composed of many tissues like mice or humans and actually treat mitochondrial disease? Stewart and his colleagues in Cologne could provide the answer. They had generated a mouse model of mitochondrial disease that contains a specific disease-causing mutation in mtDNA which leads to disorders in cardiac and muscular tissue. They treated the animals with the virus that only infected the heart or the muscles. The virus delivered the molecular scissor to cut the mutated mtDNA in the targeted tissue. And in fact, the approach worked! The levels of mutated mtDNA were reduced and the disease symptoms were alleviated.

    “This is the first gene therapy to actually remove the cause of a mitochondrial disease in a living animal” a delighted Stewart tells us. Of course, before the therapy can be applied to human patients more detailed work and safety assessments must be done. Nevertheless, the scientists could prove that they found a way to remove the cause of these mitochondrial diseases. And since there is a link between mitochondrial dysfunction and other conditions like Alzheimer’s disease, Parkinson’s disease, diabetes, and perhaps some cancers, the approach will might even have a higher impact in fighting those disorders in the future.


    Contact for scientific information:

    Dr. James Stewart
    Max Planck Institute for Biology of Ageing
    Phone: +49(0)221 379 70 706
    E-Mail: JStewart@age.mpg.de


    Original publication:

    Payam A. Gammage, Carlo Viscomi, Marie-Lune Simard, Ana S. H. Costa, Edoardo Gaude, Christopher A. Powell, Lindsey Van Haute, Beverly J. McCann, Pedro Rebelo-Guiomar, Raffaele Cerutti, Lei Zhang, Edward J. Rebar, Massimo Zeviani, Christian Frezza, James B. Stewart and Michal Minczuk: Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo. Nature Medicine, 2018 DOI: 10.1038/s41591-018-0165-9.


    Images

    A virus-infected cell in a cell culture surrounded by uninfected cells. Mitochondria are shown in green. The virus shown in orange-red (left cell) is located to the mitochondria. Scale bars: 10 μm
    A virus-infected cell in a cell culture surrounded by uninfected cells. Mitochondria are shown in gr ...
    ©Mitochondrial Biology Unit, University of Cambridge
    None


    Criteria of this press release:
    Journalists
    Biology, Medicine
    transregional, national
    Research results
    English


     

    A virus-infected cell in a cell culture surrounded by uninfected cells. Mitochondria are shown in green. The virus shown in orange-red (left cell) is located to the mitochondria. Scale bars: 10 μm


    For download

    x

    Help

    Search / advanced search of the idw archives
    Combination of search terms

    You can combine search terms with and, or and/or not, e.g. Philo not logy.

    Brackets

    You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).

    Phrases

    Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.

    Selection criteria

    You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).

    If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).