Autophagosome-like vacuole formation in Huntington's disease lymphoblasts

Research output: Contribution to journalArticle

Abstract

In an effort to clarify cellular abnormalities in Huntington's disease without the confounding factor of gross degeneration and postmortem alterations associated with studies of the brain, we have examined HD patient lymphoblasts. We report pronounced vacuole formation in patients. The vacuoles possess huntingtin remnants and cathepsin B staining, a lysosomal marker, suggesting autophagy. The number and size of vacuoles parallel the number of polyglutamine repeats in patients. Treatment with staurosporine, which augments apoptosis, leads to increased vacuole formation in Huntington's disease cells but does not influence control cells. Our findings provide direct evidence for abnormalities in Huntington's disease tissues outside the brain under basal conditions. Autophagic cellular alterations may be utilized as peripheral markers of Huntington's disease pathology.

Original languageEnglish (US)
Pages (from-to)1325-1328
Number of pages4
JournalNeuroreport
Volume15
Issue number8
DOIs
StatePublished - Jun 7 2004

Keywords

  • Autophagosome
  • Huntington's disease
  • Lymphoblasts

ASJC Scopus subject areas

  • Neuroscience(all)

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