Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Increased caspase 3 and Bax immunoreactivity accompany nuclear GAPDH translocation and neuronal apoptosis in Parkinson's disease.

      Experimental Neurology
      Aged, Aged, 80 and over, Apoptosis, physiology, Caspase 3, Caspases, metabolism, Chromatin, pathology, DNA Fragmentation, Glyceraldehyde-3-Phosphate Dehydrogenases, genetics, Humans, Infant, Middle Aged, Mitochondria, Nerve Degeneration, physiopathology, Neurons, Parkinson Disease, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-bcl-2, Signal Transduction, Substantia Nigra, Translocation, Genetic, bcl-2-Associated X Protein

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In situ end labeling combined with YOYO staining was used to mark apoptotic DNA fragmentation and chromatin condensation respectively in human postmortem brain sections. Increased numbers of apoptotic neuronal nuclei were identified in the Parkinson's disease (PD) nigra compared with age-matched controls. Caspase 3 and Bax showed increased immunoreactivity in melanized neurons of the PD nigra compared with controls. Importantly, GAPDH nuclear accumulation was also observed in the PD nigra, suggesting apoptotic rather than necrotic cell death. Interestingly, both Lewy bodies and the intranuclear Marinesco's bodies were GAPDH immunoreactive in the PD brain. Copyright 2000 Academic Press.

          Related collections

          Author and article information

          Comments

          Comment on this article