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Low dietary protein...
Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.
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Wiesner, Diana (author)
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Sinniger, Jérome (author)
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Henriques, Alexandre (author)
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Dieterlé, Stéphane (author)
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Müller, Hans-Peter (author)
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Rasche, Volker (author)
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Ferger, Boris (author)
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Dirrig-Grosch, Sylvie (author)
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- Soylu, Rana (author)
- Lund University,Lunds universitet,Translationell neuroendokrinologi,Forskargrupper vid Lunds universitet,Translational Neuroendocrinology,Lund University Research Groups
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- Petersén, Åsa (author)
- Lund University,Lunds universitet,Translationell neuroendokrinologi,Forskargrupper vid Lunds universitet,Translational Neuroendocrinology,Lund University Research Groups
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Walther, Paul (author)
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Linkus, Birgit (author)
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Kassubek, Jan (author)
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Wong, Philip C (author)
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Ludolph, Albert C (author)
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Dupuis, Luc (author)
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(creator_code:org_t)
- 2014-12-30
- 2015
- English.
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In: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 24:8, s. 2228-2240
- Related links:
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http://www.ncbi.nlm....
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http://dx.doi.org/10...
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https://academic.oup...
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https://lup.lub.lu.s...
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https://doi.org/10.1...
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Abstract
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- Mutations in components of the molecular motor dynein/dynactin lead to neurodegenerative diseases of the motor system or atypical parkinsonism. These mutations are associated with prominent accumulation of vesicles involved in autophagy and lysosomal pathways, and with protein inclusions. Whether alleviating these defects would affect motor symptoms remain unknown. Here, we show that a mouse model expressing low levels of disease linked-G59S mutant dynactin p150(Glued) develops motor dysfunction >8 months before loss of motor neurons or dopaminergic degeneration is observed. Abnormal accumulation of autophagosomes and protein inclusions were efficiently corrected by lowering dietary protein content, and this was associated with transcriptional upregulations of key players in autophagy. Most importantly this dietary modification partially rescued overall neurological symptoms in these mice after onset. Similar observations were made in another mouse strain carrying a point mutation in the dynein heavy chain gene. Collectively, our data suggest that stimulating the autophagy/lysosomal system through appropriate nutritional intervention has significant beneficial effects on motor symptoms of dynein/dynactin diseases even after symptom onset.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
Publication and Content Type
- art (subject category)
- ref (subject category)
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- By the author/editor
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Wiesner, Diana
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Sinniger, Jérome
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Henriques, Alexa ...
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Dieterlé, Stépha ...
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Müller, Hans-Pet ...
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Rasche, Volker
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show more...
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Ferger, Boris
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Dirrig-Grosch, S ...
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Soylu, Rana
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Petersén, Åsa
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Walther, Paul
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Linkus, Birgit
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Kassubek, Jan
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Wong, Philip C
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Ludolph, Albert ...
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Dupuis, Luc
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show less...
- About the subject
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- MEDICAL AND HEALTH SCIENCES
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MEDICAL AND HEAL ...
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and Basic Medicine
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and Medical Genetics
- Articles in the publication
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Human Molecular ...
- By the university
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Lund University