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Neuroreport ; 15(18): 2735-9, 2004 Dec 22.
Article in English | MEDLINE | ID: mdl-15597044

ABSTRACT

Abnormal accumulation of alpha-synuclein filaments in Lewy bodies is a neuropathological hallmark of Parkinson's disease and sequestration of cellular protein into these protein aggregates may contribute to the degenerative process. We identified the transcriptional co-factor high mobility group protein 1 (HMGB-1) as a ligand for alpha-synuclein filaments by a filament spin-down technique, mass spectrometric peptide mapping and immunoblotting. HMGB-1 binds preferentially to aggregated alpha-synuclein and is present in alpha-synuclein filament-containing Lewy bodies isolated from brain tissue affected with dementia with Lewy bodies or Parkinson's disease. Our results demonstrate that alpha-synuclein filaments hold the potential for disturbing the cellular gene expression as they can sequester a component involved in cellular transcription regulation.


Subject(s)
HMGB1 Protein/metabolism , Nerve Tissue Proteins/metabolism , Animals , Brain/metabolism , Brain/pathology , HMGB1 Protein/analysis , HMGB1 Protein/chemistry , HMGB1 Protein/ultrastructure , Humans , Immunoblotting/methods , Immunohistochemistry/methods , Iodine Isotopes/metabolism , Lewy Bodies/metabolism , Lewy Body Disease/metabolism , Ligands , Microscopy, Immunoelectron/methods , Nerve Tissue Proteins/analysis , Nerve Tissue Proteins/ultrastructure , Neurites/metabolism , Neurons/cytology , Neurons/metabolism , Parkinson Disease/metabolism , Peptide Mapping/methods , Protein Binding , Rats , Recombinant Proteins/metabolism , Synucleins , alpha-Synuclein
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