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PETBioNewsNewsNew discovery into the cause of motor neurone disease

BioNews

New discovery into the cause of motor neurone disease

Published 9 June 2009 posted in News and appears in BioNews 447

Author

Dr Charlotte Maden

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.

New findings in the research of motor neuron disease (MND) have been published in the journal Science which have greatly furthered understanding of the disease. MND is a currently incurable degenerative disorder in which motor neurons are killed so that muscles in the body are unable to...

New findings in the research of motor neuron disease (MND) have been published in the journal Science which have greatly furthered understanding of the disease.


MND is a currently incurable degenerative disorder in which motor neurons are killed so that muscles in the body are unable to be used, resulting in muscle wasting. The mind is usually unaffected, but the body has difficulties with limb mobility, speech, swallowing and breathing. The disease can affect any person at any age, and is not always inheritable. It affects about two in 100,000 people.


A team of British and Australian scientists, led by researchers at King's College London, studied a large family affected by a rare inherited form of the disease, called amyotrophic lateral sclerosis (ALS). They found that a single gene with a mutation was involved, the gene coding for the protein TDP-43. This protein was already known to accumulate in neurons in the disease. The discovery now indicates that this is not just an innocent by-product of the disease, but a critical event in the disease process, as it causes neurons to self-destruct.


Professor Chris Shaw led the team at King's College. He says the results are a 'major leap' in the right direction of curing the disease. They are the most significant since the last discoveries were made in 1993, when a gene was first linked to the disease.


The disease is related to other neurodegenerative diseases, namely Parkinson's disease, variant CJD (Creutzfeldt-Jakob disease) and Alzheimer's disease. Previously, scientists did not know the cause of over 95 per cent of cases, although genetic factors were known to be involved. Drugs for treating the disease are based on another protein, called SOD, from a gene known to be involved, but have not been beneficial to patients thus far, which triggered a push for more information.


The results can now be used to develop cellular and animal models, vital tools for scientists to study the disease, giving them a 'real chance of understanding how motor neurons degenerate', said Professor Shaw. 'This could dramatically accelerate the drug screening process', he added.


Brian Dickie is the director of research development at the MND Association, which partly funded the study. He said that he is excited by the findings, and that they are 'a spring board to greater understanding of the processes that cause motor nerves to die - and it is through such understanding that we will develop the treatment strategies to defeat this devastating disease'.

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Image by Sílvia Ferreira, Cristina Lopo and Eileen Gentleman via the Wellcome Collection. Depicts a single human stem cell embedded within a porous hydrogel matrix (false colour).
CC BY 4.0
Image by Sílvia Ferreira, Cristina Lopo and Eileen Gentleman via the Wellcome Collection. Depicts a single human stem cell embedded within a porous hydrogel matrix (false-coloured cryogenic scanning electron micrograph).
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A new research project, which will use human stem cells to artificially create the diseased brain cells affected in Motor Neurone Disease (MND) could pave the way for a cure for sufferers....

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
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9 June 2009 • 2 minutes read

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By Heidi Colleran: An international team lead by UK researchers at the Centre for Neurodegenerative Research (CNR) at Kings College, London, have discovered a genetic variation that prolongs survival in people affected with motor neuron disease (MND). In a study of over 5,000 people in six countries - almost half of...

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