BMC Cell Biology · 2008 · 26 citations · 25 references
Life SciencesCell BiologyMolecular BiologyCytoskeletonPrion DiseasesProtein FoldingFolding DiseasesPrion Protein MisfoldingProtein AggregationProtein Aggregation DisordersProtein MisfoldingProtein Misfolding DisordersAggresome FormationDisease-related Protein AggregationMisfolded Protein AggregationProteasome InhibitorsProteasome SystemProtein AggregatesProtein Misfolding PathogenesisProtein Misfolding Response
BACKGROUND: Aggresomes are juxtanuclear inclusion bodies that have been proposed to represent a general cellular response to misfolded proteins in mammalian cells. Yet, why aggresomes are not a pathological characteristic of protein misfolding diseases is unclear. Here, we investigate if a misfolded protein inevitably forms aggresomes in mammalian cells. RESULTS: We show that a cytoplasmic form of the prion protein may form aggresomes or dispersed aggregates in different cell lines. In contrast to aggresomes, the formation of dispersed aggregates is insensitive to histone deacetylase 6 inhibitors and does not result in cytoskeleton rearrangements. Modulation of expression levels or proteasome inhibitors does not alter the formation of dispersed aggregates. CONCLUSION: Our results establish that aggresomes are not obligatory products of protein misfolding in vivo.
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Stephen J. Haggarty, Kathryn M. Koeller, Jason Chun Yu Wong et al. · Proceedings of the National Academy of Sciences · 2003 · 1.1K citations · Full text