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Mutant huntingtin can paradoxically protect neurons from death

Författare

  • T Zuchner
  • Patrik Brundin

Summary, in English

Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a mutation in the gene huntingtin and characterized by motor, cognitive and psychiatric symptoms. Huntingtin contains a CAG repeat in exon 1. An expansion of this CAG repeat above 35 results in misfolding of Huntingtin, giving rise to protein aggregates and neuronal cell death. There are several transgenic HD mouse models that reproduce most of the features of the human disorder, for example protein inclusions, some neurodegeneration as well as motor and cognitive symptoms. At the same time, a subgroup of the HD transgenic mouse models exhibit dramatically reduced susceptibility to excitotoxicity. The mechanism behind this is unknown. Here, we review the literature regarding this phenomenon, attempt to explain what protein domains are crucial for this phenomenon and point toward a putative mechanism. We suggest, that the C-terminal domain of exon 1 Huntingtin, namely the proline rich domain, is responsible for mediating a neuroprotective effect against excitotoxicity. Furthermore, we point out the possible importance of this mechanism for future therapies in neurological disorders that have been suggested to be associated with excitotoxicity, for example Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis.

Publiceringsår

2008

Språk

Engelska

Sidor

435-442

Publikation/Tidskrift/Serie

Cell Death and Differentiation

Volym

15

Issue

3

Dokumenttyp

Artikel i tidskrift

Förlag

Nature Publishing Group

Ämne

  • Neurosciences

Nyckelord

  • domain
  • neuroprotection
  • proline rich
  • NMDA
  • excitotoxicity
  • Huntington's disease
  • Huntingtin

Status

Published

ISBN/ISSN/Övrigt

  • ISSN: 1350-9047